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Review

Biomaterials and Clinical Application of Dental Implants in Relation to Bone Density—A Narrative Review

by
Angkoon Khaohoen
1,
Tanapon Sornsuwan
2,
Pisaisit Chaijareenont
1,
Pongsakorn Poovarodom
1,
Chaiy Rungsiyakull
3 and
Pimduen Rungsiyakull
1,*
1
Department of Prosthodontics, Faculty of Dentistry, Chiang Mai University, Chiang Mai 50200, Thailand
2
Department of Restorative Dentistry, Faculty of Dentistry, Naresuan University, Phitsanulok 65000, Thailand
3
Department of Mechanical Engineering, Faculty of Engineering, Chiang Mai University, Chiang Mai 50200, Thailand
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2023, 12(21), 6924; https://doi.org/10.3390/jcm12216924
Submission received: 8 October 2023 / Revised: 29 October 2023 / Accepted: 2 November 2023 / Published: 3 November 2023
(This article belongs to the Special Issue New Challenges in Dental Implants)

Abstract

:
Titanium has been the material of choice for dental implant fixtures due to its exceptional qualities, such as its excellent balance of rigidity and stiffness. Since zirconia is a soft-tissue-friendly material and caters to esthetic demands, it is an alternative to titanium for use in implants. Nevertheless, bone density plays a vital role in determining the material and design of implants. Compromised bone density leads to both early and late implant failures due to a lack of implant stability. Therefore, this narrative review aims to investigate the influence of implant material/design and surgical technique on bone density from both biomechanical and biological standpoints. Relevant articles were included for analysis. Dental implant materials can be fabricated from titanium, zirconia, and PEEK. In terms of mechanical and biological aspects, titanium is still the gold standard for dental implant materials. Additionally, the macro- and microgeometry of dental implants play a role in determining and planning the appropriate treatment because it can enhance the mechanical stress transmitted to the bone tissue. Under low-density conditions, a conical titanium implant design, longer length, large diameter, reverse buttress with self-tapping, small thread pitch, and deep thread depth are recommended. Implant material, implant design, surgical techniques, and bone density are pivotal factors affecting the success rates of dental implant placement in low-density bone. Further study is required to find the optimal implant material for a clinical setting’s bone state.

1. Introduction

Dental implants generally represent the go-to procedure for replacing missing teeth because of their high success rate and attractive results. However, compromised bone quality leads to both early and late implant failures in 7.7% of cases [1]. According to this result, achieving initial stability in low-density bone, which is essential for osseointegration, is a challenging task. With the advancement of technology, numerous studies strive to enhance fixture designs and surgical techniques based on soft bone [2,3,4]. The factors that can affect the success rate of dental implants include implant material, implant design, surgical technique, patient health, or host bed [5].
Dental implant materials and designs (length, diameter, and macro- and microgeometry) affect how much stress and strain develops around the peri-implant tissue, which indicates the chance of successful osseointegration [5,6]. Consequently, the incompatibility between the elastic modulus of the implant material and bone may cause the “stress-shielding” phenomenon, which is related to peri-implant bone resorption [7,8,9]. In other words, the closer the elastic modulus implants are to the bone tissue, the better the distribution of tension. To lessen this difference, numerous studies have suggested developing either porous implants that serve as a scaffold for internal bone growth and lower the modulus of elasticity or innovative materials alloys with lower moduli [10,11,12].
Titanium has been utilized in the fabrication of dental implants since approximately 1981 [13]. According to the osseointegration concept, Brånemark first demonstrated how titanium implants induce bone integration and discovered that the titanium oxide (TiO2) layer might be responsible for establishing direct bone–implant contact [14]. Due to the TiO2 passivation coating that covers the metal surface, titanium demonstrates a strong corrosion resistance [15] in addition to desired mechanical properties, such as fatigue strength and wear resistance. Titanium and its alloys have an advantage in biological reactions due to their complete inertness in the body environment and biocompatibility [16]. Zirconia may be an alternative to titanium for individuals worried about a metallic look in the esthetic zone or metal allergies [17]. Currently, commercially available zirconia implant fixtures involve 3 mol% yttria–tetragonal zirconia polycrystal (3Y-TZP), ceria-stabilized zirconia/alumina nanocomposite (Ce-TZP/Al2O3 or NanoZR), and alumina-toughened zirconia (ATZ) [18]. Even though several studies have shown that zirconia implants have an osseointegration capacity comparable to that of titanium implants [19,20], long-term clinical data regarding mechanical [21] and biological aspects are still required.
Macrogeometry has a remarkable impact on implant stability. In cases of low-density bone, it has been proved that a conical shape achieves better initial fixation than a cylindrical design. Additionally, implant microdesign—which includes thread shape, depth, pitch, and width—is crucial for both mechanical and biological responses [22].
An additional key indicator of an implant’s success rate is the appropriate surgical technique. Various approaches are suggested by several studies to prevent failure mode, particularly in low-density bone. For instance, osseodensification is a strategy that increases drill torque without damaging biological tissue from excessively high temperatures. Under-drilling is an adaptive technique that skips the final drill protocol to enhance implant primary stability and interfacial contact. Still, the drilling guideline is debatable and frequently based on clinically perceived sensibility [2,23,24].
To reduce the high risk of implant failure associated with low bone density, researchers attempt to develop appropriate implant designs and surgical techniques to achieve the optimization guidelines for each bone condition. Nevertheless, there have been a limited number of studies regarding implant material, implant design, and surgical technique in relation to bone densities. Therefore, the purpose of this narrative review is to investigate the influence of implant material, implant design, and surgical technique on bone density from both biomechanical and biological standpoints. An additional aim is to identify the association between implant material and bone density in terms of clinical outcome.

2. Materials and Methods

The focused (PICO) question to be addressed by this review is as follows: “How do dental implant material, implant design, and surgical technique affect bone density in terms of biomechanical and biological aspects?”
P: Edentulous area treated with implant surgery.
I: Dental implant materials (titanium, zirconia, other materials).
C: Different bone densities of hard bone D1, medium bone D2–D3, soft bone D4, and cortical bone D123, no cortical D4. In this study, we classified bone densities according to high (D1–D2) and low (D3–D4).
O: Stress concentration, bone–implant interface contact (BIC), push-in values, removal torque, fracture resistance, low-temperature degradation (LTD), mean bone loss (MBL), and success and survival rates.
S: Randomized controlled or non-randomized controlled trials, case reports, animal studies, in vitro studies, finite element analysis, and review articles.
An initial electronic search of PubMed/Medline, Scopus, Embase, and other gray sources was carried out for publication dates up to 2023 with a limit of 10 years and English language search criteria. The search terms were applied in Table 1.
Included articles were those that investigated the biomaterial of dental implants related to bone mineralized density in terms of biomechanical, biological, and clinical outcomes. After preliminary searching, 529 articles were found. Duplicated articles were eliminated, and irrelevant articles were filtered out due to ineligibility based on the criteria. A total of 119 articles from the findings were included for consideration in this review. Gray literature was also taken into consideration for this analysis. For bone density in the clinical setting, 7 included articles were examined (Figure 1). Software for managing references (EndNote version 9) was employed.
After evaluating the relevant articles, the included studies were recorded on an Excel spreadsheet (Microsoft Corporation, Redmond, WA, USA). The data were grouped depending on the study design, bone types/density, dental material types, and outcome measurements such as mean bone loss, success rate, and survival rate.

3. Results

3.1. Bone Response to Dental Implant Materials

Both biomechanical and biological events can be achieved by osseointegration, referring to a direct bone–implant interface without the interposition of non-bone tissue—a higher degree of osseointegration results in the increased function and primary stability of dental implants [25]. Biomechanical factors are related to the clinical bone response to surgically placed dental implants at the time of insertion. Related factors such as surgical technique, bone density, and the utilization of adjacent graft material and device capabilities are crucial to encouraging and achieving initial bone growth. This initial stability must persist throughout the demineralization phase of bone injury. At 5 or 6 weeks, basic multicellular unit (BMU) remodeling begins, replacing the woven bone with more dense lamellar bone. The bone mineral density around the implant body was then increased for up to two years [26,27].
As well as the implant-related factor and prosthetic relevance (prosthetic design, force magnitude and direction, and load distribution) [28], one of the critical parameters for achieving both osseointegration and mechanical stability is the compatibility between the bone quality of the patient and the stiffness of the implant [9]. As a result, to optimize implant design based on the patient’s specific bone quality, the properties of the dental implant should be correspondingly adjusted.

3.1.1. Bone Density

Bone density, often known as bone quality, refers to the internal structure of bone [29]. Depending on the mechanical properties of the bone, bone quality can be divided into two aspects: density and modulus of elasticity [30]. Regarding bone structure, cortical bone is a crucial feature affecting the primary stability of implant placement, whereas cancellous bone is related to blood supply [31]. According to Misch’s classification [32], bone is categorized into the four following types according to the mineralized density and cortical thickness:
D1 bone is primarily dense cortical bone.
D2 bone comprises dense to thick, porous cortical bone with coarse trabecular bone underneath.
D3 bone is composed of thinner porous cortical bone and fine trabecular bone.
D4 bone comprises only fine trabecular bone.
Generally, the bone quality depends upon the jaw location, showing that the mandible surrounding the implant is superior in quality to the maxilla (Table 2). Significant differences exist between healthy and medically compromised subjects, age, and gender. For instance, Young’s modulus of bone can drop by up to 40 to 50% in an osteoporotic patient compared to a normal patient [33]. Regarding gender, males have higher mean bone density values at implant sites than females because of hormonal differences. Furthermore, older females have been found to have lower bone mineral densities than older males [34].
Several studies have classified bone density before implant placement based on Hounsfield units (HUs) in computer tomography (CT) examinations. Hounsfield scale is a semiquantitative technique for determining X-ray attenuation. In the HU scale, distilled water is arbitrarily assigned a value of 0 HU and air defined as −1000 HU (black on the gray scale), and characterized bone quality is represented by a value of +150 to +350 (D4), +350 to +850 (D3), +850 to +1250 (D2), and >1250 (D1) [35], as shown in Table 3. Due to its high resolution and minimized radiation exposure compared to traditional CT, cone beam computed tomography (CBCT) is one of the imaging modalities used to measure bone density. However, the gray values (GVs) from CBCT cannot be directly translated to HUs due to the lack of clinical research, which is needed to justify its use as a diagnostic tool [36,37].

3.1.2. Bone Remodeling and Bone Density

Peri-Implant Bone Strain

Mechanical loads result in bone apposition and deformation or strain, which preserve bone mass and structure through remodeling and modeling processes. Frost’s theory proposes that strain magnitude is the stimulus for bone functional adaptation. Regarding loading, the term “strain” describes the relative alteration in bone length or the deformation of bone tissue. Bone resorption occurs when the strains are between 50 and 100 microstrains. In contrast, pathologic bone occurs as microdamage or fracture if the strains have limited bone capacity or greater than 25,000 microstrains. There is a short window, between 1500 and 3000 microstrains, where non-physiologic or mild overloading causes bone gain [41,42].

Stress Distribution in Peri-Implant Bone

The density of each bone varies in strength and impacts elastic modulus, which influences the distribution of stress and strain at the bone–implant contact and the BIC (bone–implant contact) percentage. Low cancellous bone density increases bone strains while decreasing implant stability, which may result in implant failure. In addition, low bone density can also make it more challenging to place the implant in the desired location and angle. The initial bone density provides mechanical immobilization during healing and better stress transmission from the prosthesis to the bone–implant interface [43]. Consistent with previous studies [44,45], higher stress levels were observed in D4-type bone compared with the other bone types. The stress was generally concentrated in the cervical part of the implant socket. In other words, decreased bone density and cortical bone thickness increase the stress on the bone and implants, which can result in bone resorption and implant failure. On the contrary, higher bone density can provide better implant stability and a more evenly distributed occlusal load, reducing the stress and strain on the implant and the surrounding bone tissue [46].
In terms of mechanical incompatibility, differences in the elastic modulus of bone tissue and implant materials (Table 4) induce “stress shielding” by absorbing tension and transferring less stress and deformation to the bone tissue, leading to peri-implant bone loss and aseptic implant loosening [47]. In other words, the closer the elastic modulus implants are to the bone tissue, the better the distribution of tension. However, finite element analysis shows that using softer materials with similar strength to the bone provides no benefits in better stress distribution to the peri-implant bone. For example, polyetheretherketone (PEEK) material does not affect the yielding or fracture of implant components; using PEEK as an implant or abutment results in more significant deformation than titanium under static load [48]. More data from controlled clinical trials on PEEK implants are needed. Titanium alloy or zirconia implants currently remain the materials of choice due to their excellent mechanical qualities, such as stiffness. In addition, the use of advanced materials, such as nanostructured or porous materials and novel alloys, can provide a better stress distribution by reducing its elastic modulus and improving the implant’s biological response in subsequent osseointegration, particularly under compromised bone conditions. Considerably, implant design, implant location, manufacturing method, and functional graduation are also essential factors to consider in addition to implant material [12,46].
Based on a thorough assessment of the patient’s bone quality, the mechanical response of different implant designs and materials in different bone densities should be demonstrated as valuable information for clinical decision-making.

Clinical Assessment Tool

Insertion torque (IT) and resonance frequency analysis (RFA) are clinical measurements of implant stability. The insertion torque value (ITV) represents the resistance to a rotational load against the implant to the bone during implant insertion measured in Ncm [50]. According to Aparicio and colleagues, 30 to 50 Ncm provides acceptable implant stability. Some clinicians claim that a high ITV can act as a stimulus for faster osseointegration. A systematic review stated that a high ITV is required for immediate or early loading [51].
ITV, however, is largely dependent on the area of contact with bone, notably the cortical layer [52]. Moreover, the implant-cutting design capacity and bone friction are crucial determinants of distinct bone effects, resulting in high or low ITV [53]. A retrospective study [54] evaluating the mechanical effect of a drilling technique based on bone quality discovered that the bone type and implant diameter significantly influenced ITV. Compared to bone types 3 and 4, type 1 demonstrated a higher ITV. Even if the dense bone type achieves a high ITV value, the marginal bone may lose mean bone mass due to excessive stress and strain. Therefore, before implant placement in dense bone, the operator should minimize ITV to reduce the local pressure using taps or countersinking for the cortical layer.
RFA is a different technique that works by sending a frequency signal to a screwed transducer, which causes the implant to vibrate. The RFA output is expressed as an implant stability quotient (ISQ). The function of the stiffness of the bone-to-implant contact during treatment and follow-up is indicated by the greater ISQ value [55]. Several studies confirm that ISQ values below 70 and 75 at implant placement or after 3–4 months of healing indicate implants with a higher risk of failure [24,56].
Removal torque (RTQ) is a destructive test determining the critical torque value for disrupting the bone-to-implant interlocking by unscrewing the implant. This test, unutilized in clinical research, can be used to assess the quality of osseointegration in terms of bone-to-implant contact. Like the ITV, the RTQ is influenced by bone quality, implant geometry, and implant stability [57,58].

Histological Assessment Tool

The higher ISQ value indicates the function of the stiffness of the BIC. The BIC ratio is correlated with the biomechanical properties of the bone-to-implant interface and increases during bone healing [59]. Histological analysis of bone-to-implant interfaces has determined the presence of mineralized tissue in contact with the implant surface rather than fibrous tissue. Nonetheless, it is still being determined how the BIC % can be translated into osseointegration [60]. According to Albrektsson and coworkers [61], good integration accounts for 60% of BIC. Different results can be obtained depending on the bone type, healing time, and implant type.

3.2. Material Used for Dental Implants and Their Properties

Titanium has recently become the material of choice for dental implant fixtures due to its exceptional qualities and excellent balance of rigidity and stiffness. Since zirconia is a soft-tissue-friendly material and caters to aesthetic demands, it is an alternative material to titanium implants. Additionally, PEEK is a polymer material with excellent mechanical properties and superior biocompatibility because it has a low Young’s modulus comparable to surrounding bone, which influences an optimal load transfer [62].

3.2.1. Biomaterial of Dental Implants

Metal and Metal Alloy

Titanium and Ti-6Al-4V
Titanium is a frequently used material for dental implants, mainly because of its biocompatibility and capacity to promote osseointegration. The ability of titanium metal to react with air and generate hydroxyl and hydroxide groups endows it with a high capacity for resisting corrosion. This reaction results in the formation of titanium dioxide, which is the most reported in dental implant fields [63]. Currently, there are four grades of commercially pure titanium (CpTi), ranging in purity from 98.0% to 99.6% and processing oxygen content, as well as two different types of titanium alloys made of Ti-6Al-4V and Ti-6Al-4V Extra-Low Interstitial alloys in mechanical properties, such as strength, ductility, and corrosion resistance [64].
Grade IV CpTi is the most commonly utilized variety due to its high oxygen content (0.4%) and, thus, excellent mechanical strength. The alloy Ti-6Al-4V, often known as grade V titanium, is widely used in orthopedics because of its superior strength and lower Young’s modulus [13]. However, aluminum (Al) and vanadium (V) may affect bone mineralization and type IV allergic reactions, respectively [65]. To avoid an adverse biological response, vanadium-free alloys and non-toxic components such as Nb, Ta, Zr, and Pd are being developed [64].
Titanium and Titanium–Zirconium Alloy
A novel alloy (Roxolid®, Straumann, Basel, Switzerland: TiZr1317) has been produced based on the binary formation of 83–87% titanium and 13–17% zirconium [66]. It outperforms CpTi and Ti-6Al-4V in terms of tensile (953 MPa) and fatigue strength (230 N) [67]. Furthermore, this alloy material exhibits good biocompatibility as pure titanium [68].
Titanium Alloys in 3D Printing
In recent years, 3D printing technologies, also known as additive manufacturing (AM) technologies, have been successfully applied in implant dentistry because they are the alternative method for generating implant products. Moreover, they have allowed for the fabrication of custom implants with microscale resolution. Metallic implants were frequently created using selective laser fusion (SLM) and electron beam fusion (EBM) procedures [69].

Ceramics

For people concerned about a metallic appearance in the esthetic zone or metal allergies, ceramics are an alternative material to titanium [4]. Ceramics are known as inert materials and have good physical properties. They are widely used as a coating material for metal implants [70] and a substrate for fabricating dental implants [71]. Presently, commercially available zirconia implant fixtures involve Y-TZP and ATZ. Details on the manufacturer, brand name, material, and design of the zirconia implant system are given by Ban [18].
Yttria–Tetragonal Zirconia Polycrystal (Y-TZP)
Zirconium dioxide (ZrO2), often known as zirconia, is a polymorphic material occurring in three temperature-dependent forms: monoclinic (stable from room temperature to 1170 °C), tetragonal (from 1170 to 2370 °C), and cubic (from 2370 °C to the melting point, 2680 °C). When cooling, there is a significant alteration in zirconia unit cell volume, resulting in structural defects that affect the mechanical properties. Because of the spontaneous phase shift of zirconia from tetragonal to monoclinic, doping agents (CaO, MgO, Y2O3) are used to stabilize the structure to create partially stabilized zirconia (PSZ) or tetragonal zirconia polycrystal (TZP) [72,73]. The microstructure of 3Y-TZP ceramics for dental applications comprises 3 mol% yttria as a stabilizer and up to 98% small equiaxed tetragonal grains, occasionally with a small amount of cubic phase. The mechanical characteristics of 3Y-TZP depend on the grain size, determined by the sintering temperature [74,75]. Recently, Y-TZP used as an oral implant material has demonstrated exceptionally high strength (>1200 MPa) [76]. Nevertheless, low-temperature degradation or aging can reduce the fracture resistance of the material [77] and generate microcracks or micro-roughness on the surface caused by a spontaneous and progressively change in Zr2O grains from the tetragonal to the monoclinic phase in the presence of water molecules. Then, moisture can seep deeper into the material, accelerating the aging phenomenon [78]. A novel ceria-stabilized zirconia-based composite was developed to reduce the aging in dental ceramics [79] that is not prone to aging due to the stabilization using cerium rather than yttrium [80]. According to an in vitro investigation, this innovative zirconia-based composite is appropriate for reduced-diameter one-piece design implants in the anterior jaw regions [81].
Alumina-Toughened Zirconia (ATZ)
ATZ, a zirconia–alumina composite, is a composite ceramic material of 20 vol% alumina and 80 vol% zirconia with 3 mol% yttria. The addition of alumina significantly improves flexural strength, fracture toughness, and resistance of the material to surface degradation [82]

Polyetheretherketone (PEEK)

PEEK has been used as an alternative to metals for implants since 1998. It has emerged as an option for individuals desiring metal-free restorations in cases of bruxism and allergic responses. Due to its stiff semicrystalline nature, hardness resembling bone, excellent mechanical capabilities, and superior biocompatibility, PEEK is employed as a biomaterial for implant rehabilitation [62].
PEEK material has a Young’s modulus of 3.6 GPa in pure form, 18 GPa in carbon-reinforced PEEK (CFR-PEEK), and 12 GPa in glass fiber-reinforced PEEK (GFR-PEEK) [49]. Because PEEK has Young’s modulus close to that of bone, it allows for better dispensation of masticatory force around the implant and exhibits less stress shielding than titanium implants [83].
Most polymers, such as PEEK, have low surface energy, making them bioinert, and do not provide osteoconductive properties. As a result, PEEK stimulates less osteoblast differentiation than titanium [62]. To induce more bone formation on the PEEK surface, various modifications such as hydroxyapatite (HA)-covered PEEK, TiO2 coating on PEEK, or sandblasting (nFA/PEEK) can improve the PEEK surface by rendering it more biologically compatible [84].
Furthermore, PEEK influences biofilm structure and reduces the potential of peri-implant inflammation. However, because there have been very few clinical trials on PEEK as a dental implant, conclusive evidence is awaited on whether it can truly replace titanium as a dental implant [62].

3.2.2. Functional Properties of Dental Implant Materials to Bone Density

The mechanical properties of implant materials, such as stiffness, strength, ductility, and toughness, describe their capacity to withstand forces and displacements measured by uniaxial tensile tests [85]. Stress, which defines the force applied to a material, is classified into three types: tensile, compressive, and shear.
Strength is generally defined as the ability of the prosthesis to withstand applied stress without fracture (ultimate strength) or permanent deformation (yield strength). As a property, strength is not as reliable for estimating the survival probabilities of brittle material prostheses over time compared to fracture toughness, which more clearly describes the resistance to crack propagation of brittle materials [86]. Flexural strength, also called bending strength or modulus of rupture, is a strength test of the material’s ability to sustain bending forces applied perpendicular to its longitudinal axis [87].
Elastic modulus, measured by the ratio of elastic stress to elastic strain, is a term used to describe a material’s relative stiffness or rigidity. This property impacts the strength and fatigue strength of the materials as well as the functionality of manufactured implants [47].
Ductility represents the ability of a material to resist a sizeable permanent deformation under a tensile load up to the point of fracture. For example, material A is the most ductile, as shown by the most extended plastic strain range. In contrast, material B is brittle, defined as having no plastic deformation and breaking at the proportional limit [86].
The overall area between the elastic and plastic zones, from zero stress to fracture stress, is related to toughness. Fracture toughness measures the energy required to propagate critical flaws in the structure. For instance, a tough material is generally strong, whereas a strong material is not necessarily tough [86].

Elastic Modulus, Stiffness

After an implant completes osseointegration, the chewing stress is transferred to the bone tissue surrounding the implant body. As a result of the mismatch between the stiffness of the implant material and the peri-implant bone, the stress imbalance can lead to marginal bone loss and implant failure [88]. This stress-induced marginal bone destruction can be described using the “composite beam analysis” principle. In the case of two materials with different elastic moduli, the primary point of contact between the two materials is where the greatest stress is concentrated [89]. According to Hooke’s law, material stiffness depends on its modulus. In the case of the bone–implant system, the bone tends to create more significant deformations. Thus, controlling the variables determining how to reduce the transferred stress is critical, including load type, implant treatment protocol, design component, and peri-implant bone quality [90]. Ti-6Al-4V alloy is the most frequently utilized in the fabrication of dental implants because of its superior elastic modulus and tensile strength [91]. In cases of limited bone availability, a rigid alloy called “Ti-Zr” has been developed [92]. Zirconia implants, such as Y-TZP, have become more popular as aesthetic concerns have increased. To improve the elastic properties to more closely resemble the characteristics of pristine bone with better biomimetics and biocompatibility, many researchers have attempted to develop novel alloys [93] or improve the implant surface characteristics (porosity) [94,95]. Therefore, by reducing the stiffness of the implant materials, many studies have attempted to determine the optimal mechanical characteristics of titanium-based materials. To modify its mechanical properties, alloy elements are often added, including Nb, Zr, Ta, and Sn. Furthermore, producing a porous structure employing 3D printing technology lessens implant stiffness, improves stress transmission, and accelerates the formation of new bone and osseointegration [47].
PEEK is widely used to replace titanium or zirconia implant materials because carbon fiber can be added to it to produce carbon fiber PEEK (CFR-PEEK) with varying elastic moduli, which are within the range of the bones’ elastic modulus [96,97]. Interestingly, 30% carbon fibers PEEK (30CFR-PEEK) shows higher stress concentration and deformation at the bone–implant interface, even though reinforcing PEEK with carbon and glass fiber—by determining the optimum quantity, size, and shape of carbon fibers—is the most effective way to improve mechanical properties and prevent stress shielding. However, these drawbacks can be lessened using 60% carbon fibers PEEK (60CFR-PEEK) [98]. In clinical settings, PEEK is expected to replace titanium and zirconia implant materials due to its low stress shielding. Furthermore, PEEK has greater application benefits for patients with poor bone conditions, bruxism, and esthetic concerns [99]. The functional properties of various implant materials are presented in Table 5.
The implant geometry significantly affects the implant treatment because it can enhance the mechanical stress transmitted to the bone tissue, causing marginal bone loss [100]. To be more precise, unbalanced load distribution can be improved by modifying implant macro- or microgeometries. According to one literature review, a hybrid design, which combines conical and cylindrical forms, has the highest primary stability because it can distribute stresses more uniformly and incorporate more bone. A conical design, which is wider at the base and narrower at the top, also provides better initial stability and load distribution. This result can reduce marginal bone loss when compared to a cylindrical form [101]. In cases requiring immediate implant insertion, conical implant systems with double threads and a low thread helix angle should be used [102]. In addition to implant shape, a previous study concluded that primary stability significantly increases with implant length. Longer implants can affix to more bone in soft bone situations because they have a greater surface area for osseointegration, increasing primary stability. Nevertheless, different implant lengths and diameters do not appreciably alter the primary stability properties in environments of dense bone [103]. Diameter becomes a more decisive factor as soon as implant length is sufficient since the stress occurs at the implant neck, where bone loss initiates at an early implantation stage. In soft bone, wider-diameter implants improve primary stability and functional surface area, allowing even load distribution [104].
The implant’s thread design is crucial for its early mechanical primary and ensuing secondary biological stability [105]. Dental implants with a narrow pitch have an increased implant surface and more threads per implant length, which might improve load distribution [106].
The higher the thread depth, the more the surface and the load distribution increase. Greater thread depths may benefit the more excellent functional surface, particularly with softer bone and high occlusal stresses [107], while axial forces distributed as compressive forces with square and buttress threads can be transformed into shear and compressive forces using V-shaped reverse buttress threads [108]. Thread designs with a depth of 0.34 to 0.5 mm and a width of 0.18 to 0.3 mm are reportedly advantageous [108]. Moreover, the thread’s face angle directly controls how much force the implant applies to the surrounding bone [109]. The optimal pitch, with more than 0.8 mm and greater thread-to-thread spacing, can increase resistance to vertical stresses [108]. A few studies from the review period used zirconia or PEEK implant materials to investigate the relationship between implant shape and bone density. However, there was some advice that the diameter of the zirconia implant should exceed 3.25 mm to sufficiently occupy the deep thread depth. Additionally, the cylindrical form design for the zirconia implant should be low-density.
The summary of implant geometries associated with the bone densities in each implant material is displayed in Table 6.
The overall success of dental implants also depends on other factors, including the type of implant, prosthetic connection, and the surgical technique.
First, the implant types can be categorized into one-piece and two-piece implants. Microgaps between the implant fixture and the abutment in two-piece dental implants have been associated with microleakage and bacterial contamination [110]. According to the in silico study [111], in comparison to one-piece dental implants, there were higher stress values found in the crestal bone surrounding two-piece implants. These results are used to explain the higher levels of peri-implant marginal bone loss in two-piece dental implants compared to one-piece implants.
Second, many studies have compared external and internal connection types of implants. A retrospective study compared survival rate and peri-implant marginal bone loss between different types of connections. Marginal bone loss was higher in the area around the implants with an external abutment connection after the 1-year follow-up. After five years, there was no apparent distinction between the groups with internal and external connections [112]. A systematic review compared the platform-switching and non-platform-switching implants in terms of crestal bone loss. This result confirmed that platform-switched implants are useful in clinical settings and can help to prevent bone loss around the implants [113].
Thirdly, the surgical technique plays a critical role in achieving primary stability when placing dental implants in bone that is primarily composed of medullary tissue (D3-D4). There are various surgical techniques suggested to enhance the primary stability in the low-density bone, such as undersized drilling, osteotome technique, piezoelectric bone surgery, and magnetodynamic surgery. Several studies have proved that osseodensification, underpreparation, or expander techniques improved the primary stability of low-density bone, while conventional drilling obtained lower ISQ values [2,3]. A systematic review found that while piezoelectric inserts may speed up the bone healing process, they do not affect the primary mechanical stability [114]. Recently, several authors have explored the application of magnetodynamic technology in implant rehabilitation. An in vitro study assessed the initial stability of two surgical techniques in low-density bone. Compared to the conventional method, magnetodynamic surgery seems to provide higher IT, ISQ, and RT values [115].
Table 5. Functional properties of implant materials.
Table 5. Functional properties of implant materials.
PropertiesElastic Modulus (GPa)Flexural/Tensile Strength (MPa)Yield Strength (MPa)Fracture Strength (N)Surface RoughnessThermal ConductivityHydrophobicityRef.
TicpTi
(IV)
104.1680485-More than Zr and PEEKYesNo[116,117]
TiAl6V4110954729-[118]
Ti-Zr96953--[116,119]
Ti-24Nb-4Zr-8Sn (Ti2448)45850--[120]
Zr3Y210900–1200-516–607LessLowNo[121]
ATZ2201800–2400-1064–1734[121]
PEEKPEEK3–480--LessLowYes[121,122]
CFR-PEEK18120--[121,122]
GFR-PEEK12---[96,121]
Table 6. Implant geometries related to the bone densities [22,47,102].
Table 6. Implant geometries related to the bone densities [22,47,102].
Titanium Implant MacrogeometryMicrogeometry
(Thread Design)
Bone DensityImplant Placement ConditionShapeDiameterLengthShapePitchWidthDepth
High-
-
Cylindrical
-
Conical
-
Hybrid design (apical conical and crestal cylindrical)
AllAll
(≥6 mm)
-
V-thread
-
Square thread
-
Buttress thread
Standard (1.2 mm)Standard (0.18–0.30 mm)Standard (0.42 mm)
Low-
-
Conical
-
Conical with crestal back taper
-
Cylindrical design with apical taper
Wider
(≥4 mm)
Longer
(9–11 mm)
-
Reverse buttress
-
Self-tapping
🡇
Lower than the standard
Standard🡅
Higher than the standard
-Immediate
-
Conical
≥4 mm≥11 mm
-
Self-tapping
---

Fracture Resistance

ISO 14801:2016 [123] describes a method for evaluating fracture resistance appropriate for in vitro testing. Several studies have been conducted to assess the fracture resistance behaviors (including fracture load and survival probability) of dental implants.
Implant-supported restoration using a titanium abutment and metal–ceramic crown, which has a high success rate of about 95%, is one of the traditional treatment options of choice [124]. Due to its outstanding esthetics, biocompatibility, and mechanical properties, zirconia is a considerably suitable material for constructing implant abutments or crowns in the anterior region [125]. Several studies have investigated the fracture resistance of zirconia as an abutment and values above the occlusal forces applied in the anterior section were achieved. This finding is consistent with Agustin-Panadero et al. [126], who compared the fracture resistance and failure mode of esthetic crown materials (zirconia, lithium disilicate, nanoceramic resin) and confirmed that all zirconia abutments with the three different crown materials, can withstand the physiological loads that occur in the anterior region. However, zirconia abutments bearing zirconia crowns exhibited the lowest fracture resistance (459.63 ± 66.52 N), and the most common fracture locations were the screw (80%) and abutment (15%). Focusing on the titanium implant connection interface, the interconnection between the same material outperformed zirconia abutments in fit and experienced less wear [127].
The literature has evaluated zirconia implants for their fracture resistance based on various criteria, including material selection, design, manufacturing, and restoration. Kohal et al. compared fracture strength between one-piece ATZ and Y-TZP ceramic implants [128]. The results showed that ATZ has higher mechanical stability than Y-TZP and can withstand functional loads for an anticipated 20 years. Hanes and colleagues [129] investigated the fracture resistance characteristics of titanium–zirconium, one-piece zirconia, and two-piece zirconia implants restored with zirconia crowns. The results showed that titanium–zirconium implants with prefabricated titanium abutments and zirconia crowns had higher peak fracture loads (942 ± 241 N) and better survival probability behavior than the one-piece and two-piece zirconia implants. Moreover, one-piece zirconia implants with zirconia crowns and two-piece zirconia implants with screw-retained zirconia crowns on prefabricated titanium abutment had comparable peak fracture loads (645 ± 165 N vs. 650 ± 124 N) and survival probability behavior.
A systematic meta-analysis investigated the effects of different treatments (dynamic loading, hydrothermal aging) and implant attributes (material, design, or manufacturing procedures) on the fracture resistance of zirconia implants. Regarding material, the AZT implant was more fracture-resistant than the Y-TZP implant using a one-piece design. Nonetheless, there was no statistically significant difference between the two-piece designs of ATZ and Y-TZP implants. The multi-material complex of the available two-piece zirconia implants may have caused different aging degradation behaviors under treatments (hydrothermal aging or dynamic loading). Finally, the implant components may fracture after static loading [130]. In the instance of two-piece zirconia implants combined with three distinct abutment screw materials (gold, titanium, and PEEK), there were no significant differences in fracture load among materials. The PEEK screw, however, showed inferior results. As previously stated, the evidence implies that a two-piece ATZ implant system assembled with a PEEK abutment screw is not inferior to a two-piece titanium implant in terms of its fracture resistance [131].
For implants, a one-piece design was found to be more fracture-resistant than a two-piece design [130]. Although one-piece zirconia overcame two-piece zirconia in terms of fracture resistance and insusceptibility to low-temperature degradation due to the lack of potential stress concentration at the interface and screw attachment, the lack of flexibility for detailed adjustments resulted in clinical problems for the surgeon and prosthodontist; for example, it represents a potential limitation when trying to compensate for mal-positioned implants [21]. The two-piece implant system has recently played an outstanding role on the market, but there is limited long-term clinical data and fracture analyses. The clinical fracture analysis of one-piece and two-piece zirconia implants was evaluated by Zhang et al. [21]. They found that the fracture initiation site of one-piece implants originated in the constriction area between two threads in the endosseous component. For two-piece implants, three distinct fracture initiation sites were observed at the abutment neck, internal abutment–implant connections or implant–screw connection (inner threads), and the implant body in the endosseous part. According to the investigation, the abutment neck of one-piece zirconia implants is one of the areas of stress concentration. In contrast, for two-piece zirconia implants, the quality of the abutment surface seems critically important.
The macro-design of zirconia implants is an essential parameter to consider when deciding on a system. Zirconia implants with a diameter less than or equal to 3.25 mm, a profound thread depth, and a sharp or pointed thread design are not clinically advisable due to local stress concentration [132].
Other factors affecting the fracture resistance of zirconia have been investigated, in which no statistically significant difference was found in the fracture resistance due to manufacturing method, use of different implant diameters (3.8–4.5 mm), and treatment by thermal aging or dynamic loading [130].

3.2.3. Biological Properties of Dental Implant Materials to Bone Density

Biological reactions at the implant surface and bone contact are critical to the longevity of implant osseointegration and the function of the prostheses. The titanium surface interacts with water molecules and mineral ions during surgery. The surface polarity shifts and the plasma protein (albumin) binds to the surface. After that, the plasma proteins placed by the extracellular matrix protein (vitronectin) aid in cell adhesion. Cells attach to the titanium surface by binding to the vitronectin coating and other extracellular matrix proteins. After one week of implant insertion, the first bone, known as the “woven bone”, contacts the implant surface. The woven bone is then replaced by lamellar bone via the process of bone remodeling. This process may continue for years, depending on the stress distribution surrounding the implant and the bone [133,134].
Titanium is a well-known biomaterial for dental implants since it is inert and does not stimulate foreign body responses. The biomaterial serves as a scaffold for bone growth. The biomaterial’s macro- and microporosity allows osteogenic cells and blood vessels to invade, proliferate, and differentiate inside the biomaterial particles. Several surface modification techniques have been developed to improve the surface biocompatibility and bone response surrounding the implant, allowing for faster osseointegration and early loading [135].
Zirconia implants have been investigated in recent years. Zirconia is a chemically inert biomaterial with minimal local or systemic adverse effects, good cell adhesion, great tissue response, and biocompatibility with the nearby bone and soft tissue [132]. Numerous studies have shown that zirconia implants have an osteoconductive characteristic after implantation and do not have any cytotoxic effects on the bone or fibroblast [71]. Koch et al. [136] investigated the osseointegration of one-piece zirconia and titanium implants. After four months, there were no significant differences in bone level in the crestal aspect concerning material type. With the same surface modification and roughness, zirconia implants could achieve near BIC rates comparable to titanium implants. In terms of bacterial adhesion, the presence of Gram-negative anaerobic bacteria is closely linked with peri-mucositis and peri-implantitis. According to an in vitro study that evaluated the growth of biofilms on various implant materials, zirconia implants had either a comparable level or significantly less bacterial colonization than titanium implants [137]. The recommended materials for the fabrication of implant-supported prostheses are zirconia and titanium.
PEEK is a potential alternative material that has been utilized in dental implantology due to some negative aspects of titanium, including esthetic expectations, hypersensitivity reactions, and stress-shielding phenomena [96]. Even though this material has excellent biocompatibility and no cytotoxicity, it performs poorly osseointegration than titanium due to lower BIC area, less osteoblast differentiation, and less osteoconductive [96,136]. Increases in the hydrophilicity and roughness of PEEK materials can be generated via nanoscale surface treatments to overcome these drawbacks.
The surface characteristics of materials (Table 5), such as hydrophilicity, surface roughness, and surface modification [138], affect the rate and quality of osseointegration. For instance, there is better osseointegration on hydrophilic surfaces than on hydrophobic surfaces. The biological properties of various implant materials are shown in Table 7.
An increasing number of surface modifications are being introduced despite the majority of studies comparing machined surfaces with new rough surfaces [140]. Shalabi and coworkers [141] found positive correlations between surface roughness, bone-to-implant contact, and pushout strength. Surface roughness enhances osseointegration, stimulating bone formation and preventing bone resorption. Albrektsson and Wennerberg [142] classified the roughness of implant surfaces into four groups: smooth surfaces (Sa value of <0.5 µm), minimally rough surfaces (Sa value of 0.5–1 µm), moderately rough surfaces (Sa value of 1–2 µm), and rough surfaces (Sa value of >2 µm). There is currently consensus for titanium implants that a moderately rough surface with a Sa of 1 to 2 µm has the highest osseointegration potential [140]. However, this dogma may not apply to zirconia implants [143]. Subtractive and additive methods, influencing different orientations and roughness, are frequently employed to change the topography of surfaces, as shown in Table 8. Subtraction requires eliminating particles from the implant’s surface to leave pits or pores. Meanwhile, the additive approach involves adding material to the implant surface to provide a bumpy texture [140].
There are many techniques for modifying the topography of titanium implant surfaces, including mechanical, chemical, electrochemical, and layer addition [144]. Blasting and polishing are the mechanical processes most frequently used to alter a metallic surface [145]. Numerous studies have shown that the rate of osseointegration improves after treatment [146,147]. In addition, a more recent method called UV light functionalization produces micro- and nanostructured surface roughness in only the inner part of the thread, allowing for bone formation. This approach facilitates hastened osseointegration of titanium into bone [148]. Zirconia implant surfaces are treated similarly to titanium surfaces. According to clinical observations, acid etching after sandblasting resulted in the highest implant survival rate and the least mean bone loss. Sinter, slurry-modified, and sandblasted surfaces are the second and third most positive results, respectively. However, sandblasting followed by an acid etching technique produces an equivalent result to the sinter and slurry techniques regarding bone-to-implant contact. Therefore, one-piece zirconia with a sandblasted and etched surface treatment currently has the highest survival rates [143]. Several methods can be used to enhance the roughness and surface energy of PEEK materials, such as HA coating, UV light treatments, and TiO2 coating [138]. However, most studies on osseointegration and in vitro investigations on PEEK implants have considered only short-term consequences.
An overview of titanium, zirconia, and PEEK as dental implant materials in clinical settings is shown in Table 9.

3.3. Clinical Application of Dental Implants and Their Survival Rates

3.3.1. Survival Rate of Alternative Implant Materials

A significant factor determining the long-term success rate of implants is peri-implant mean boss loss. According to the guidelines of the consensus report of the First European Workshop on Periodontology, successful results are achieved when bone decreases of less than 1.5 mm are noted during the first year of functional loading and 0.2 mm annual bone loss is observed [149]. Many studies have reported the success rate of dental implant materials in clinical settings. Long-term usage of titanium implants has demonstrated the material’s excellent success rate in various applications [150], including single/partial implant-supported restorations, removable implant-retained/supported overdenture, and fixed implant-supported prostheses. In the past decade, zirconia implants have been employed as an alternative to titanium implants when patients have metal allergies or esthetic concerns. Zirconia has equivalent biological, physical, and biocompatibility properties to titanium [17]. In addition to material selection, several manufacturers have tried to modify the surface topography using subtractive and additive techniques to improve their properties [143]. Meta-analyses of clinical trials on alternative implant materials and success rates are summarized in Table 10.
The findings of two systematic reviews reported the overall survival rate of zirconia implants after 1 to 7.8 years of observation. Adanez and colleagues [152] found that zirconia implants had a 95% survival rate (76% to 100%) after 1 to 7 years of surveillance. In terms of implant design, one-piece designs had a survival rate of 95% (95% Cl 91–97%) following 1 to 7 years of monitoring. The two-piece designs had an overall survival rate of 94% (95% CI 87–97%) after observation periods of between 1 and 3 years. They also observed a failure rate of 6.44% for one-piece designs and 13.66% for two-piece designs. After one year, the mean MBL of zirconia implants was 0.89 mm (95% CI 0.60–1.18). According to Borges et al. [151], the overall mean MBL was 0.80 mm (95% CI: 0.60 to 1.00) and 1.01 (95% CI: 0.72 to 1.29) after 1- and 2-year observation periods, consecutively. The survival rate ranged from 71.2% at one year to 100% at 7.8 years. In conclusion, zirconia implants, particularly one-piece designs, demonstrated acceptable survival and marginal bone loss values in short-term (1-year) monitoring periods, consistent with the standard consensus [149]. However, due to a lack of clinical support, they did not suggest using two-piece zirconia in clinical settings.
Bone augmentation or narrow-diameter dental implants (NDIs) are alternative options for treatment when there is not enough bone for placing regular-diameter implants. Nevertheless, patients with parafunctional habits or areas with a high occlusal load have serious concerns about the resistance and strength of NDIs [153]. A Ti-Zr alloy was created (Roxolid; Institute Straumann AG, Basel, Switzerland) to enhance mechanical strength and biocompatibility [154]. Altuna et al. [155] concluded that narrow-diameter Ti-Zr dental implants had survival and success rates (>95%) and marginal bone loss (<1 mm) equivalent to those of regular-diameter titanium implants in the short term.

3.3.2. Survival Rate of Dental Implants Related to Bone Density

Bone density is a significant variable for anticipating stress–strain distribution at the peri-implant area, influencing bone modeling and remodeling and, consequently, the success or failure rates of dental implants. Furthermore, the difference in stiffness between implant material and peri-implant bone causes marginal bone loss and aseptic implant loosening due to stress-shielding phenomena.
Concerning bone density, mean bone loss after implant placement determines the clinical success rate of dental implant materials. Our review focuses on the factors, such as material types, properties, and bone densities (according to Misch’s classification [35]), that influence clinical outcome parameters, as indicated in Table 11. Unclear or undefined bone quality is not included in this table.
The seven included studies selected for analysis were published between 2012 and 2022 and had data regarding bone qualities according to Misch’s classification. Only one study (n = 18) evaluated zirconia material in environments of low bone density. Other studies (n = 398) examined the effects of titanium under different bone conditions. The evaluated studies had follow-up periods varying between three and twelve months.
The level of peri-implant bone loss is measured based on periapical films using the parallel technique. Regardless of the material and follow-up period, low bone quality (D3/4) tended to have more MBL than high bone quality (D1/2) [156,157,158,159,160,161]. For instance, the mean MBL reduction reported by Held et al. [119], at roughly 1.46 mm, is close to the borderline value recommendation (1.50 mm). However, the data suggested that the hydrophilic implants have good osseointegration characteristics even in low-quality bone. This finding is consistent with a previous systematic analysis, which found that the survival rates of dental implants depending on the bone density were type I, 97.6%; type II, 96.2%; type III, 96.5%; and type IV, 88.8%. Additionally, compared to machined surface implants, treated surface implants had a greater survival rate (97.1%) when placed in low-density bone. This higher survival rate may explain the surface treatment’s role in facilitating tighter cell–titanium interactions, which enhance the bone tissue’s biological and biomechanical effects [162].
Table 11. Clinical parameters of dental materials related to bone density in the included studies.
Table 11. Clinical parameters of dental materials related to bone density in the included studies.
Study/YearStudy TypeMaterialImplantSurface SiteGeometryMean MBL
(Mean ± SD)
Follow-Up
(Month)
Aldebes et al. 2022 [163]RCTsOne-piece zirconia (Y-TZP)18Sandblasting surfacePremolarAnatomic zirconia implantD3/4: 0.61 ± 0.2312
Makary et al. 2019 [156]CT 16 D1: 0.20 ± 0.2712
Titanium23Ca2+ on the SLA-treated surfaceAllDifferent diameters of 4, 4.5, 5, 5.5 mm with 10 mm lengthD2/3: 0.11 ± 0.11
7 D4: 0.33 ± 0.14
Hingsammer et al. 2017 [157]CT 15 D1: 0.66 ± 0.7212
Titanium38TiUnite surface and machine neckPosteriorShort implantsD2/3: 0.60 ± 0.77
21 D4: 0.65 ± 0.68
De Santis et al. 2016 [158]CTTitanium35TiUnite surfaceAllTapered and double-variable thread design, apical drilling bladesD2/3: 0.68 ± 0.656
109 D4: 0.73 ± 0.46
Cannizzaro et al. 2012 [159]RCTsTitanium68Dual etched and
covered with nanoscale
calcium phosphate crystal
Immediate loading site 4 mm diameter with tapered-with external connectionD123: 0.26 ± 0.356
Rossi et al. 2014 [160]CTTitanium31SLActive surface with moderate roughPosterior6 mm length with 4.1 and 4.8 mm diameterD123: 0.55 ± 0.8012
Held et al. 2013 [161]CTTitanium35Sandblasted and acid-etched surfaceAllELEMENT RC implants with 4, 4.5, 5 mm diameter and 8, 9.5, 11.5, 12, 14 mm lengthD3/4: 1.46 ± 0.753
Aldebes et al. [163] observed that the mean MBL of one-piece modified anatomic zirconia implants was 0.61 mm in the low bone type. The findings also indicated that the one-piece design and zirconia implant material, considered tissue-friendly and biocompatible, may offset lower MBL. As a result, changes in the peri-implant bone density or the level of bone-to-implant contact are indicators of the implants’ osseointegration abilities. Makaray et al. [156] did show, however, that IT values might be regulated by matching implant geometry to bone type. High IT values did not impact marginal bone levels when using a specific implant design.

4. Conclusions

-
Implant material, implant design, and surgical techniques are pivotal factors affecting the success rates of dental implant placement in low-density bone.
-
Both titanium and zirconia implants are widely accepted materials in the market. Nonetheless, PEEK implants serve as an alternative material for specific cases, such as those involving poor bone conditions, bruxism, and esthetic concerns.
-
Modified implant topography, strengthened implant geometry, and a suitable surgical technique are selected and used to achieve high survival and success rates and attain superior clinical results.
-
In low-density conditions,
o
Titanium provides a better chance of achieving initial stability due to the best mechanical performance among the three materials.
o
Conical titanium implant design, wider diameter, longer length, reverse buttress with self-tapping, small thread pitch, and deep thread depth are recommended.
o
Surgical techniques, such as underpreparation, osteotome technique, and magnetodynamic surgery, play a critical role in achieving primary stability. However, piezoelectric surgery does not affect the initial stability but does affect the secondary stability.
-
Regardless of the material and follow-up period, low bone quality tended to have more marginal bone loss than high bone quality.
-
Further study is required to identify an optimal implant material in terms of the bone state in clinical settings.

Author Contributions

Conceptualization, A.K. and P.R.; methodology, A.K. and P.R.; software, A.K.; validation, P.R., P.C., A.K. and C.R.; formal analysis, A.K. and P.R.; investigation, A.K. and P.R.; resources, A.K., P.R. and C.R.; data curation, A.K., and P.R.; writing—original draft preparation, A.K.; writing—review and editing, A.K., P.R., P.C., T.S. and P.P.; visualization, P.R., C.R., T.S. and P.P.; supervision, P.R.; project administration, P.R.; funding acquisition, P.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Chiang Mai University, Thailand.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

This research was supported by the TA/RA Scholarship from Graduate School, Chiang Mai University, Chiang Mai, Thailand.

Conflicts of Interest

The authors declare no conflict of interest.

Lists of Abbreviations

AbbreviationsExplanation
TiO2Titanium oxide
3Y-TZP3 mol% yttria–tetragonal zirconia polycrystal
ATZAlumina-toughened zirconia
BICBone–implant interface contact
LTDLow-temperature degradation
HUsHounsfield units
CTComputer tomography
CBCTCone beam computed tomography
GVsGray values
PEEKPolyetheretherketone
ITInsertion torque
RFAResonance frequency analysis
ISQImplant stability quotient
RTQRemoval torque
SLM Selective laser fusion
EBMElectron beam fusion
ZrO2Zirconium dioxide
PSZPartially stabilized zirconia
TZPTetragonal zirconia polycrystal
CFR-PEEKCarbon fiber reinforcement polyetheretherketone
GFR-PEEKGlass fiber reinforcement polyetheretherketone
GPaGigapascal
Ti6Al4VTitanium–6 Aluminum–4 Vanadium
CpTiCommercially pure titanium
HAHydroxyapatite
TPSTitanium plasma-sprayed
UVUltraviolet
RCTsRandomized Clinical Trials
Non-RCTNon-Randomized Clinical Trial

References

  1. Esposito, M.; Hirsch, J.M.; Lekholm, U.; Thomsen, P. Biological factors contributing to failures of osseointegrated oral implants. (I). Success criteria and epidemiology. Eur. J. Oral Sci. 1998, 106, 527–551. [Google Scholar] [CrossRef] [PubMed]
  2. Olmedo-Gaya, M.-V.; Romero-Olid, M.-N.; Ocaña-Peinado, F.M.; Vallecillo-Rivas, M.; Vallecillo, C.; Reyes-Botella, C. Influence of different surgical techniques on primary implant stability in the posterior maxilla: A randomized controlled clinical trial. Clin. Oral Investig. 2023, 27, 3499–3508. [Google Scholar] [CrossRef] [PubMed]
  3. Al Ahmari, N.M. Osseo-densification versus conventional surgical technique in low density jaw bone: A split mouth in vivo study. Technol. Health Care 2022, 30, 1117–1124. [Google Scholar] [CrossRef] [PubMed]
  4. Mello-Machado, R.C.; Sartoretto, S.C.; Granjeiro, J.M.; Calasans-Maia, J.A.; de Uzeda, M.J.P.G.; Mourão, C.F.A.B.; Ghiraldini, B.; Bezerra, F.J.B.; Senna, P.M.; Calasans-Maia, M.D. Osseodensification enables bone healing chambers with improved low-density bone site primary stability: An in vivo study. Sci. Rep. 2021, 11, 15436. [Google Scholar] [CrossRef]
  5. Javed, F.; Ahmed, H.B.; Crespi, R.; Romanos, G.E. Role of primary stability for successful osseointegration of dental implants: Factors of influence and evaluation. Interv. Med. Appl. Sci. IMAS 2013, 5, 162–167. [Google Scholar] [CrossRef] [PubMed]
  6. Bozkaya, D.; Muftu, S.; Muftu, A. Evaluation of load transfer characteristics of five different implants in compact bone at different load levels by finite elements analysis. J. Prosthet. Dent. 2004, 92, 523–530. [Google Scholar] [CrossRef] [PubMed]
  7. Tretto, P.H.W.; Dos Santos, M.B.F.; Spazzin, A.O.; Pereira, G.K.R.; Bacchi, A. Assessment of stress/strain in dental implants and abutments of alternative materials compared to conventional titanium alloy-3D non-linear finite element analysis. Comput. Methods Biomech. Biomed. Eng. 2020, 23, 372–383. [Google Scholar] [CrossRef] [PubMed]
  8. Robau-Porrua, A.; Pérez-Rodríguez, Y.; Soris-Rodríguez, L.M.; Pérez-Acosta, O.; González, J.E. The effect of diameter, length and elastic modulus of a dental implant on stress and strain levels in peri-implant bone: A 3D finite element analysis. Biomed. Mater. Eng. 2020, 30, 541–558. [Google Scholar] [CrossRef]
  9. Gupta, Y.; Iyer, R.; Dommeti, V.K.; Nutu, E.; Rana, M.; Merdji, A.; Biswas, J.K.; Roy, S. Design of dental implant using design of experiment and topology optimization: A finite element analysis study. Proc. Inst. Mech. Eng. H 2021, 235, 157–166. [Google Scholar] [CrossRef]
  10. Liu, B.; Xu, W.; Chen, M.; Chen, D.; Sun, G.; Zhang, C.; Pan, Y.; Lu, J.; Guo, E.; Lu, X. Structural Design and Finite Element Simulation Analysis of Grade 3 Graded Porous Titanium Implant. Int. J. Mol. Sci. 2022, 23, 10090. [Google Scholar] [CrossRef]
  11. Piotrowski, B.; Baptista, A.A.; Patoor, E.; Bravetti, P.; Eberhardt, A.; Laheurte, P. Interaction of bone-dental implant with new ultra low modulus alloy using a numerical approach. Mater. Sci. Eng. C Mater. Biol. Appl. 2014, 38, 151–160. [Google Scholar] [CrossRef]
  12. Dias Corpa Tardelli, J.; Monteiro de Barros Ciribelli Alves, B.; Lima da Costa Valente, M.; Cândido dos Reis, A. Influence of the modulus of elasticity of dental implants on the distribution of stresses in the alveolar bone by the finite element method: A systematic review. J. Oral Maxillofac. Surg. Med. Pathol. 2023, 35, 383–389. [Google Scholar] [CrossRef]
  13. Nicholson, J.W. Titanium Alloys for Dental Implants: A Review. Prosthesis 2020, 2, 100–116. [Google Scholar] [CrossRef]
  14. Brånemark, P.I. Osseointegration and its experimental background. J. Prosthet. Dent. 1983, 50, 399–410. [Google Scholar] [CrossRef] [PubMed]
  15. Alghamdi, H.S.; Jansen, J.A. The development and future of dental implants. Dent. Mater. J. 2020, 39, 167–172. [Google Scholar] [CrossRef] [PubMed]
  16. Liu, X.; Chu, P.K.; Ding, C. Surface modification of titanium, titanium alloys, and related materials for biomedical applications. Mater. Sci. Eng. R Rep. 2004, 47, 49–121. [Google Scholar] [CrossRef]
  17. Comisso, I.; Arias-Herrera, S.; Gupta, S. Zirconium dioxide implants as an alternative to titanium: A systematic review. J. Clin. Exp. Dent. 2021, 13, e511–e519. [Google Scholar] [CrossRef] [PubMed]
  18. Ban, S. Classification and Properties of Dental Zirconia as Implant Fixtures and Superstructures. Materials 2021, 14, 4879. [Google Scholar] [CrossRef]
  19. Pieralli, S.; Kohal, R.J.; Jung, R.E.; Vach, K.; Spies, B.C. Clinical Outcomes of Zirconia Dental Implants: A Systematic Review. J. Dent. Res. 2017, 96, 38–46. [Google Scholar] [CrossRef]
  20. Pieralli, S.; Kohal, R.J.; Lopez Hernandez, E.; Doerken, S.; Spies, B.C. Osseointegration of zirconia dental implants in animal investigations: A systematic review and meta-analysis. Dent. Mater. 2018, 34, 171–182. [Google Scholar] [CrossRef]
  21. Zhang, F.; Monzavi, M.; Li, M.; Čokić, S.; Manesh, A.; Nowzari, H.; Vleugels, J.; Van Meerbeek, B. Fracture analysis of one/two-piece clinically failed zirconia dental implants. Dent. Mater. 2022, 38, 1633–1647. [Google Scholar] [CrossRef] [PubMed]
  22. Heimes, D.; Becker, P.; Pabst, A.; Smeets, R.; Kraus, A.; Hartmann, A.; Sagheb, K.; Kämmerer, P.W. How does dental implant macrogeometry affect primary implant stability? A narrative review. Int. J. Implant Dent. 2023, 9, 20. [Google Scholar] [CrossRef] [PubMed]
  23. Stacchi, C.; Troiano, G.; Montaruli, G.; Mozzati, M.; Lamazza, L.; Antonelli, A.; Giudice, A.; Lombardi, T. Changes in implant stability using different site preparation techniques: Osseodensification drills versus piezoelectric surgery. A multi-center prospective randomized controlled clinical trial. Clin. Implant Dent. Relat. Res. 2022, 25, 133–140. [Google Scholar] [CrossRef]
  24. Giudice, A.; Bennardo, F.; Antonelli, A.; Barone, S.; Wagner, F.; Fortunato, L.; Traxler, H. Influence of clinician’s skill on primary implant stability with conventional and piezoelectric preparation techniques: An ex-vivo study. J. Biol. Regul. Homeost. Agents 2020, 34, 739–745. [Google Scholar] [CrossRef] [PubMed]
  25. Meyer, U.; Joos, U.; Mythili, J.; Stamm, T.; Hohoff, A.; Fillies, T.; Stratmann, U.; Wiesmann, H.P. Ultrastructural characterization of the implant/bone interface of immediately loaded dental implants. Biomaterials 2004, 25, 1959–1967. [Google Scholar] [CrossRef] [PubMed]
  26. Ferguson, S.J.; Langhoff, J.D.; Voelter, K.; von Rechenberg, B.; Scharnweber, D.; Bierbaum, S.; Schnabelrauch, M.; Kautz, A.R.; Frauchiger, V.M.; Mueller, T.L.; et al. Biomechanical comparison of different surface modifications for dental implants. Int. J. Oral Maxillofac. Implant 2008, 23, 1037–1046. [Google Scholar]
  27. Piattelli, A. Bone Response to Dental Implant Materials; Woodhead Publishing: Sawston, UK, 2016. [Google Scholar]
  28. Elsayed, M. Biomechanical factors that influence the bone-implant-interface. Res. Rep. Oral Maxillofac. Surg. 2019, 3, 1–14. [Google Scholar]
  29. Misch, C.E. Density of bone: Effect on treatment plans, surgical approach, healing, and progressive boen loading. Int. J. Oral Implantol. 1990, 6, 23–31. [Google Scholar]
  30. Misch, C. Available bone influences prosthodontic treatment. Dent. Today 1988, 7, 44–75. [Google Scholar]
  31. Lekholm, U. Patient selection and preparation. In Tissue Integrated Prostheses: Osseointegration in Clinical Dentistry; Branemark, P.I., Zarb, G.A., Albrektsson, T., Eds.; Quintessence Publishing Company: Chicago, IL, USA, 1985. [Google Scholar]
  32. Misch, C. Bone character: Second vital implant criterion. Dent. Today 1988, 7, 39. [Google Scholar]
  33. Roy, S.; Das, M.; Chakraborty, P.; Biswas, J.K.; Chatterjee, S.; Khutia, N.; Saha, S.; Chowdhury, A.R. Optimal selection of dental implant for different bone conditions based on the mechanical response. Acta Bioeng. Biomech. 2017, 19, 11–20. [Google Scholar] [PubMed]
  34. Turkyilmaz, I.; McGlumphy, E.A. Influence of bone density on implant stability parameters and implant success: A retrospective clinical study. BMC Oral Health 2008, 8, 32. [Google Scholar] [CrossRef] [PubMed]
  35. Misch, C.E. Density of bone: Effect on surgical approach, and healing. In Contemporary Implant Dentistry; Lippincott Williams & Wilkins, Inc.: Philadelphia, PA, USA, 1999; pp. 371–384. [Google Scholar]
  36. Eguren, M.; Holguin, A.; Diaz, K.; Vidalon, J.; Linan, C.; Pacheco-Pereira, C.; Lagravere Vich, M.O. Can gray values be converted to Hounsfield units? A systematic review. Dentomaxillofacial Radiol. 2022, 51, 20210140. [Google Scholar] [CrossRef] [PubMed]
  37. Patrick, S.; Birur, N.P.; Gurushanth, K.; Raghavan, A.S.; Gurudath, S. Comparison of gray values of cone-beam computed tomography with hounsfield units of multislice computed tomography: An in vitro study. Indian J. Dent. Res. 2017, 28, 66. [Google Scholar] [PubMed]
  38. Lim Fat, D.; Kennedy, J.; Galvin, R.; O’Brien, F.; Mc Grath, F.; Mullett, H. The Hounsfield value for cortical bone geometry in the proximal humerus—An in vitro study. Skelet. Radiol. 2012, 41, 557–568. [Google Scholar] [CrossRef] [PubMed]
  39. Aamodt, A.; Kvistad, K.A.; Andersen, E.; Lund-Larsen, J.; Eine, J.; Benum, P.; Husby, O.S. Determination of the Hounsfield value for CT-based design of custom femoral stems. J. Bone Jt. Surgery. Br. Vol. 1999, 81, 143–147. [Google Scholar] [CrossRef]
  40. Ahmed, M.; Ikram, Y.; Qureshi, F.; Sharjeel, M.; Khan, Z.A.; Ataullah, K. Assessment of Jaw Bone Density in Terms of Hounsfield Units Using Cone Beam Computed Tomography for Dental Implant Treatment Planning. Pak. Armed Forces Med. J. 2021, 71, 221–227. [Google Scholar] [CrossRef]
  41. Frost, H.M. Wolff’s Law and bone’s structural adaptations to mechanical usage: An overview for clinicians. Angle Orthod 1994, 64, 175–188. [Google Scholar]
  42. Frost, H.M. From Wolff’s law to the Utah paradigm: Insights about bone physiology and its clinical applications. Anat. Rec. 2001, 262, 398–419. [Google Scholar] [CrossRef]
  43. Demenko, V.; Linetsky, I.; Nesvit, V.; Linetska, L.; Shevchenko, A. FE study of bone quality effect on load-carrying ability of dental implants. Comput. Methods Biomech. Biomed. Eng. 2014, 17, 1751–1761. [Google Scholar] [CrossRef]
  44. Leblebicioğlu Kurtuluş, I.; Kilic, K.; Bal, B.; Kilavuz, A. Finite Element Analysis of the Stress Distribution Associated With Different Implant Designs for Different Bone Densities. J. Prosthodont. 2022, 31, 614–622. [Google Scholar] [CrossRef] [PubMed]
  45. Rungsiyakull, P.; Rungsiyakull, C.; Monstaporn, M.; Sae-Lee, D.; Elsaka, S. Effects of bone type and occlusal loading pattern on bone remodeling in implant-supported single crown: A finite element study. J. Prosthodont. 2023. [Google Scholar] [CrossRef] [PubMed]
  46. Yalçın, M.; Kaya, B.; Laçin, N.; Arı, E. Three-Dimensional Finite Element Analysis of the Effect of Endosteal Implants with Different Macro Designs on Stress Distribution in Different Bone Qualities. Int. J. Oral Maxillofac. Implant 2019, 34, e43–e50. [Google Scholar] [CrossRef] [PubMed]
  47. Li, J.; Jansen, J.A.; Walboomers, X.F.; van den Beucken, J.J. Mechanical aspects of dental implants and osseointegration: A narrative review. J. Mech. Behav. Biomed. Mater. 2020, 103, 103574. [Google Scholar] [CrossRef]
  48. Al-Mortadi, N.; Bataineh, K.; Albakri, I. A Three–Dimensional Finite Element Analysis of Polyetheretherketone PEEK in Dental Implant Prosthesis: A Novel Implant System. Open Dent. J. 2022, 16, e187421062203040. [Google Scholar] [CrossRef]
  49. Lee, W.T.; Koak, J.Y.; Lim, Y.J.; Kim, S.K.; Kwon, H.B.; Kim, M.J. Stress shielding and fatigue limits of poly-ether-ether-ketone dental implants. J. Biomed. Mater. Res. B Appl. Biomater. 2012, 100, 1044–1052. [Google Scholar] [CrossRef] [PubMed]
  50. Friberg, B.; Sennerby, L.; Gröndahl, K.; Bergström, C.; Bäck, T.; Lekholm, U. On cutting torque measurements during implant placement: A 3-year clinical prospective study. Clin. Implant Dent. Relat. Res. 1999, 1, 75–83. [Google Scholar] [CrossRef]
  51. Esposito, M.; Grusovin, M.G.; Willings, M.; Coulthard, P.; Worthington, H.V. The effectiveness of immediate, early, and conventional loading of dental implants: A Cochrane systematic review of randomized controlled clinical trials. Int. J. Oral Maxillofac. Implant 2007, 22, 893–904. [Google Scholar]
  52. Norton, M. Primary stability versus viable constraint—A need to redefine. Int. J. Oral Maxillofac. Implant 2013, 28, 19–21. [Google Scholar]
  53. Stocchero, M. On Influence of Undersized Implant Site On Implant Stability and Osseointegration; Faculty of Odontology, Malmö University: Malmö, Sweden, 2018. [Google Scholar]
  54. Toia, M.; Stocchero, M.; Cecchinato, F.; Corrà, E.; Jimbo, R.; Cecchinato, D. Clinical Considerations of Adapted Drilling Protocol by Bone Quality Perception. Int. J. Oral Maxillofac. Implant 2017, 32, 1288–1295. [Google Scholar] [CrossRef]
  55. Turkyilmaz, I.; Sennerby, L.; Yilmaz, B.; Bilecenoglu, B.; Ozbek, E.N. Influence of defect depth on resonance frequency analysis and insertion torque values for implants placed in fresh extraction sockets: A human cadaver study. Clin. Implant Dent. Relat. Res. 2009, 11, 52–58. [Google Scholar] [CrossRef] [PubMed]
  56. Andersson, P.; Pagliani, L.; Verrocchi, D.; Volpe, S.; Sahlin, H.; Sennerby, L. Factors Influencing Resonance Frequency Analysis (RFA) Measurements and 5-Year Survival of Neoss Dental Implants. Int. J. Dent. 2019, 2019, 3209872. [Google Scholar] [CrossRef] [PubMed]
  57. Atsumi, M.; Park, S.H.; Wang, H.L. Methods used to assess implant stability: Current status. Int. J. Oral Maxillofac. Implant 2007, 22, 743–754. [Google Scholar]
  58. Johansson, C.; Albrektsson, T. Integration of screw implants in the rabbit: A 1-year follow-up of removal torque of titanium implants. Int. J. Oral Maxillofac. Implant 1987, 2, 69–75. [Google Scholar]
  59. Mathieu, V.; Vayron, R.; Soffer, E.; Anagnostou, F.; Haïat, G. Influence of healing time on the ultrasonic response of the bone-implant interface. Ultrasound Med. Biol. 2012, 38, 611–618. [Google Scholar] [CrossRef] [PubMed]
  60. Masuda, T.; Yliheikkilä, P.K.; Felton, D.A.; Cooper, L.F. Generalizations regarding the process and phenomenon of osseointegration. Part I. In vivo studies. Int. J. Oral Maxillofac. Implant 1998, 13, 17–29. [Google Scholar]
  61. Albrektsson, T.; Eriksson, A.R.; Friberg, B.; Lekholm, U.; Lindahl, L.; Nevins, M.; Oikarinen, V.; Roos, J.; Sennerby, L.; Astrand, P. Histologic investigations on 33 retrieved Nobelpharma implants. Clin. Mater. 1993, 12, 1–9. [Google Scholar] [CrossRef]
  62. Mishra, S.; Chowdhary, R. PEEK materials as an alternative to titanium in dental implants: A systematic review. Clin. Implant Dent. Relat. Res. 2019, 21, 208–222. [Google Scholar] [CrossRef]
  63. Chen, X.; Mao, S.S. Titanium dioxide nanomaterials: Synthesis, properties, modifications, and applications. Chem. Rev. 2007, 107, 2891–2959. [Google Scholar] [CrossRef]
  64. Osman, R.B.; Swain, M.V. A Critical Review of Dental Implant Materials with an Emphasis on Titanium versus Zirconia. Materials 2015, 8, 932–958. [Google Scholar] [CrossRef]
  65. Morais, L.S.; Serra, G.G.; Muller, C.A.; Andrade, L.R.; Palermo, E.F.A.; Elias, C.N.; Meyers, M. Titanium alloy mini-implants for orthodontic anchorage: Immediate loading and metal ion release. Acta Biomater. 2007, 3, 331–339. [Google Scholar] [CrossRef]
  66. Silva, R.C.S.; Agrelli, A.; Andrade, A.N.; Mendes-Marques, C.L.; Arruda, I.R.S.; Santos, L.R.L.; Vasconcelos, N.F.; Machado, G. Titanium Dental Implants: An Overview of Applied Nanobiotechnology to Improve Biocompatibility and Prevent Infections. Materials 2022, 15, 3150. [Google Scholar] [CrossRef] [PubMed]
  67. Grandin, H.M.; Berner, S.; Dard, M. A Review of Titanium Zirconium (TiZr) Alloys for Use in Endosseous Dental Implants. Materials 2012, 5, 1348–1360. [Google Scholar] [CrossRef]
  68. Chiapasco, M.; Casentini, P.; Zaniboni, M.; Corsi, E.; Anello, T. Titanium-zirconium alloy narrow-diameter implants (Straumann Roxolid(®)) for the rehabilitation of horizontally deficient edentulous ridges: Prospective study on 18 consecutive patients. Clin. Oral Implant Res. 2012, 23, 1136–1141. [Google Scholar] [CrossRef] [PubMed]
  69. Oliveira, T.T.; Reis, A.C. Fabrication of dental implants by the additive manufacturing method: A systematic review. J. Prosthet. Dent. 2019, 122, 270–274. [Google Scholar] [CrossRef]
  70. Campbell, A.A. Bioceramics for implant coatings. Mater. Today 2003, 6, 26–30. [Google Scholar] [CrossRef]
  71. Kohal, R.J.; Att, W.; Bächle, M.; Butz, F. Ceramic abutments and ceramic oral implants. An update. Periodontology 2000 2008, 47, 224–243. [Google Scholar] [CrossRef] [PubMed]
  72. Neacşu, I.A.; Nicoară, A.I.; Vasile, O.R.; Vasile, B.Ş. Chapter 9—Inorganic micro- and nanostructured implants for tissue engineering. In Nanobiomaterials in Hard Tissue Engineering; Grumezescu, A.M., Ed.; William Andrew Publishing: Norwich, NY, USA, 2016; pp. 271–295. [Google Scholar] [CrossRef]
  73. Jitwirachot, K.; Rungsiyakull, P.; Holloway, J.A.; Jia-mahasap, W. Wear Behavior of Different Generations of Zirconia: Present Literature. Int. J. Dent. 2022, 2022, 9341616. [Google Scholar] [CrossRef] [PubMed]
  74. Ruiz, L.; Readey, M.J. Effect of Heat Treatment on Grain Size, Phase Assemblage, and Mechanical Properties of 3 mol% Y-TZP. J. Am. Ceram. Soc. 1996, 79, 2331–2340. [Google Scholar] [CrossRef]
  75. Jia-mahasap, W.; Jitwirachot, K.; Holloway, J.A.; Rangsri, W.; Rungsiyakull, P. Wear of various restorative materials against 5Y-ZP zirconia. J. Prosthet. Dent. 2022, 128, 814.e1–814.e10. [Google Scholar] [CrossRef]
  76. Lorusso, F.; Noumbissi, S.; Francesco, I.; Rapone, B.; Khater, A.G.A.; Scarano, A. Scientific Trends in Clinical Research on Zirconia Dental Implants: A Bibliometric Review. Materials 2020, 13, 5534. [Google Scholar] [CrossRef] [PubMed]
  77. Chevalier, J.; Loh, J.; Gremillard, L.; Meille, S.; Adolfson, E. Low-temperature degradation in zirconia with a porous surface. Acta Biomater. 2011, 7, 2986–2993. [Google Scholar] [CrossRef] [PubMed]
  78. Chevalier, J.; Gremillard, L.; Virkar, A.V.; Clarke, D.R. The Tetragonal-Monoclinic Transformation in Zirconia: Lessons Learned and Future Trends. J. Am. Ceram. Soc. 2009, 92, 1901–1920. [Google Scholar] [CrossRef]
  79. Palmero, P.; Fornabaio, M.; Montanaro, L.; Reveron, H.; Esnouf, C.; Chevalier, J. Towards long lasting zirconia-based composites for dental implants. Part I: Innovative synthesis, microstructural characterization and in vitro stability. Biomaterials 2015, 50, 38–46. [Google Scholar] [CrossRef] [PubMed]
  80. Altmann, B.; Karygianni, L.; Al-Ahmad, A.; Butz, F.; Bächle, M.; Adolfsson, E.; Fürderer, T.; Courtois, N.; Palmero, P.; Follo, M.; et al. Assessment of Novel Long-Lasting Ceria-Stabilized Zirconia-Based Ceramics with Different Surface Topographies as Implant Materials. Adv. Funct. Mater. 2017, 27, 1702512. [Google Scholar] [CrossRef]
  81. Burkhardt, F.; Harlass, M.; Adolfsson, E.; Vach, K.; Spies, B.C.; Kohal, R.-J. A Novel Zirconia-Based Composite Presents an Aging Resistant Material for Narrow-Diameter Ceramic Implants. Materials 2021, 14, 2151. [Google Scholar] [CrossRef] [PubMed]
  82. Pabst, W.; Havrda, J.; Gregorová, E.; Krcmova, B. Alumina toughened zirconia made by room temperature extrusion of ceramic pastes. Ceram.-Silikáty 2000, 44, 41–47. [Google Scholar]
  83. Schwitalla, A.D.; Spintig, T.; Kallage, I.; Müller, W.D. Flexural behavior of PEEK materials for dental application. Dent. Mater. 2015, 31, 1377–1384. [Google Scholar] [CrossRef]
  84. Rahmitasari, F.; Ishida, Y.; Kurahashi, K.; Matsuda, T.; Watanabe, M.; Ichikawa, T. PEEK with Reinforced Materials and Modifications for Dental Implant Applications. Dent. J. 2017, 5, 35. [Google Scholar] [CrossRef]
  85. Wegst, U.G.; Bai, H.; Saiz, E.; Tomsia, A.P.; Ritchie, R.O. Bioinspired structural materials. Nat. Mater. 2015, 14, 23–36. [Google Scholar] [CrossRef]
  86. Anusavice, K.J.; Shen, C.; Rawls, H.R. Phillips’ Science of Dental Materials; Elsevier Health Sciences: Amsterdam, The Netherlands, 2012. [Google Scholar]
  87. Campo, E.A. 2—Mechanical Properties of Polymeric Materials. In Selection of Polymeric Materials; Campo, E.A., Ed.; William Andrew Publishing: Norwich, NY, USA, 2008; pp. 41–101. [Google Scholar] [CrossRef]
  88. Wiskott, H.A.; Belser, U.C. Lack of integration of smooth titanium surfaces: A working hypothesis based on strains generated in the surrounding bone. Clin. Oral Implant Res. 1999, 10, 429–444. [Google Scholar] [CrossRef] [PubMed]
  89. Kitamura, E.; Stegaroiu, R.; Nomura, S.; Miyakawa, O. Influence of marginal bone resorption on stress around an implant--a three-dimensional finite element analysis. J. Oral Rehabil. 2005, 32, 279–286. [Google Scholar] [CrossRef] [PubMed]
  90. Kozlovsky, A.; Tal, H.; Laufer, B.Z.; Leshem, R.; Rohrer, M.D.; Weinreb, M.; Artzi, Z. Impact of implant overloading on the peri-implant bone in inflamed and non-inflamed peri-implant mucosa. Clin. Oral Implant Res. 2007, 18, 601–610. [Google Scholar] [CrossRef] [PubMed]
  91. Niinomi, M. Recent Research and Development in Titanium Alloys for Biomedical Applications and Healthcare Goods. Sci. Technol. Adv. Mater. 2003, 4, 445–454. [Google Scholar] [CrossRef]
  92. Lee, T.J.; Ueno, T.; Nomura, N.; Wakabayashi, N.; Hanawa, T. Titanium-Zirconium Binary Alloy as Dental Implant Material: Analysis of the Influence of Compositional Change on Mechanical Properties and In Vitro Biologic Response. Int. J. Oral Maxillofac. Implant 2016, 31, 547–554. [Google Scholar] [CrossRef] [PubMed]
  93. Guo, Y.; Chen, D.; Cheng, M.; Lu, W.; Wang, L.; Zhang, X. The bone tissue compatibility of a new Ti35Nb2Ta3Zr alloy with a low Young’s modulus. Int. J. Mol. Med. 2013, 31, 689–697. [Google Scholar] [CrossRef] [PubMed]
  94. Palmquist, A.; Snis, A.; Emanuelsson, L.; Browne, M.; Thomsen, P. Long-term biocompatibility and osseointegration of electron beam melted, free-form-fabricated solid and porous titanium alloy: Experimental studies in sheep. J. Biomater. Appl. 2013, 27, 1003–1016. [Google Scholar] [CrossRef] [PubMed]
  95. Pérez-Pevida, E.; Brizuela-Velasco, A.; Chávarri-Prado, D.; Jiménez-Garrudo, A.; Sánchez-Lasheras, F.; Solaberrieta-Méndez, E.; Diéguez-Pereira, M.; Fernández-González, F.J.; Dehesa-Ibarra, B.; Monticelli, F. Biomechanical Consequences of the Elastic Properties of Dental Implant Alloys on the Supporting Bone: Finite Element Analysis. BioMed Res. Int. 2016, 2016, 1850401. [Google Scholar] [CrossRef]
  96. Najeeb, S.; Zafar, M.S.; Khurshid, Z.; Siddiqui, F. Applications of polyetheretherketone (PEEK) in oral implantology and prosthodontics. J. Prosthodont. Res. 2016, 60, 12–19. [Google Scholar] [CrossRef]
  97. Guo, Y.; Chen, C.; Zhang, S.; Ren, L.; Zhao, Y.; Guo, W. Mediation of mechanically adapted TiCu/TiCuN/CFR-PEEK implants in vascular regeneration to promote bone repair in vitro and in vivo. J. Orthop. Transl. 2022, 33, 107–119. [Google Scholar] [CrossRef]
  98. Souza, J.C.M.; Pinho, S.S.; Braz, M.P.; Silva, F.S.; Henriques, B. Carbon fiber-reinforced PEEK in implant dentistry: A scoping review on the finite element method. Comput. Methods Biomech. Biomed. Eng. 2021, 24, 1355–1367. [Google Scholar] [CrossRef] [PubMed]
  99. Chen, M.; Ren, M.; Shi, Y.; Liu, X.; Wei, H. State-of-the-art polyetheretherketone three-dimensional printing and multifunctional modification for dental implants. Front. Bioeng. Biotechnol. 2023, 11, 1271629. [Google Scholar] [CrossRef]
  100. El-Anwar, M.I.; El-Zawahry, M.M.; Ibraheem, E.M.; Nassani, M.Z.; ElGabry, H. New dental implant selection criterion based on implant design. Eur. J. Dent. 2017, 11, 186–191. [Google Scholar] [CrossRef] [PubMed]
  101. Kim, J.M.; Kim, S.J.; Han, I.; Shin, S.W.; Ryu, J.J. A comparison of the implant stability among various implant systems: Clinical study. J. Adv. Prosthodont. 2009, 1, 31–36. [Google Scholar] [CrossRef] [PubMed]
  102. Righesso, L.; Blatt, S.; Kwon, Y.-D.; Al-Nawas, B. Primärstabilität dentaler Implantate—Eine Übersichtsarbeit. Implantologie 2016, 24, 261–268. [Google Scholar]
  103. Staedt, H.; Kämmerer, P.W.; Goetze, E.; Thiem, D.G.E.; Al-Nawas, B.; Heimes, D. Implant primary stability depending on protocol and insertion mode—An ex vivo study. Int. J. Implant Dent. 2020, 6, 49. [Google Scholar] [CrossRef] [PubMed]
  104. Steigenga, J.T.; al-Shammari, K.F.; Nociti, F.H.; Misch, C.E.; Wang, H.L. Dental implant design and its relationship to long-term implant success. Implant Dent. 2003, 12, 306–317. [Google Scholar] [CrossRef]
  105. Soto-Peñaloza, D.; Caneva, M.; Viña-Almunia, J.; Martin-de-Llano, J.J.; García-Mira, B.; Peñarrocha-Oltra, D.; Botticelli, D.; Peñarrocha-Diago, M. Effect on osseointegration of two implant macro-designs:A histomorphometric analysis of bicortically installed implants in different topographic sites of rabbit’s tibiae. Med. Oral Patol. Oral Cir. Bucal. 2019, 24, e502–e510. [Google Scholar] [CrossRef]
  106. Chun, H.J.; Cheong, S.Y.; Han, J.H.; Heo, S.J.; Chung, J.P.; Rhyu, I.C.; Choi, Y.C.; Baik, H.K.; Ku, Y.; Kim, M.H. Evaluation of design parameters of osseointegrated dental implants using finite element analysis. J. Oral Rehabil. 2002, 29, 565–574. [Google Scholar] [CrossRef]
  107. Lee, S.Y.; Kim, S.J.; An, H.W.; Kim, H.S.; Ha, D.G.; Ryo, K.H.; Park, K.B. The effect of the thread depth on the mechanical properties of the dental implant. J. Adv. Prosthodont. 2015, 7, 115–121. [Google Scholar] [CrossRef]
  108. Abuhussein, H.; Pagni, G.; Rebaudi, A.; Wang, H.L. The effect of thread pattern upon implant osseointegration. Clin. Oral Implant Res. 2010, 21, 129–136. [Google Scholar] [CrossRef]
  109. Tumedei, M.; Petrini, M.; Pietropaoli, D.; Cipollina, A.; La Torre, C.; Di Carmine, M.S.; Piattelli, A.; Iezzi, G. The Influence of the Implant Macrogeometry on Insertion Torque, Removal Torque, and Periotest Implant Primary Stability: A Mechanical Simulation on High-Density Artificial Bone. Symmetry 2021, 13, 776. [Google Scholar] [CrossRef]
  110. Kadkhodazadeh, M.; Safi, Y.; Moeintaghavi, A.; Amid, R.; Baghani, M.T.; Shidfar, S. Marginal Bone Loss Around One-Piece Implants: A 10-Year Radiological and Clinical Follow-up Evaluation. Implant Dent. 2019, 28, 237–243. [Google Scholar] [CrossRef] [PubMed]
  111. Wu, A.Y.; Hsu, J.T.; Chee, W.; Lin, Y.T.; Fuh, L.J.; Huang, H.L. Biomechanical evaluation of one-piece and two-piece small-diameter dental implants: In-vitro experimental and three-dimensional finite element analyses. J. Formos. Med. Assoc. 2016, 115, 794–800. [Google Scholar] [CrossRef] [PubMed]
  112. Kim, Y.M.; Lee, J.B.; Um, H.S.; Chang, B.S.; Lee, J.K. Long-term effect of implant-abutment connection type on marginal bone loss and survival of dental implants. J. Periodontal. Implant Sci. 2022, 52, 496–508. [Google Scholar] [CrossRef] [PubMed]
  113. Gupta, J. Safety and sagacious use of remdesivir: Paramount focus on contemporary perspectives. Ann. Afr. Med. 2019, 18, 1–6. [Google Scholar] [CrossRef] [PubMed]
  114. Shadid, R.M.; Sadaqah, N.R.; Othman, S.A. Does the Implant Surgical Technique Affect the Primary and/or Secondary Stability of Dental Implants? A Systematic Review. Int. J. Dent. 2014, 2014, 204838. [Google Scholar] [CrossRef] [PubMed]
  115. Antonelli, A.; Barone, S.; Attanasio, F.; Salviati, M.; Cerra, M.G.; Calabria, E.; Bennardo, F.; Giudice, A. Effect of Implant Macro-Design and Magnetodynamic Surgical Preparation on Primary Implant Stability: An In Vitro Investigation. Dent. J. 2023, 11, 227. [Google Scholar] [CrossRef] [PubMed]
  116. Bernhard, N.; Berner, S.; de Wild, M.; Wieland, M. The binary TiZr Alloy—A newly developed Ti alloy for use in dental implants. Forum Implantol. 2009, 5, 30–39. [Google Scholar]
  117. Sarraf, M.; Rezvani Ghomi, E.; Alipour, S.; Ramakrishna, S.; Liana Sukiman, N. A state-of-the-art review of the fabrication and characteristics of titanium and its alloys for biomedical applications. Bio-Des. Manuf. 2022, 5, 371–395. [Google Scholar] [CrossRef]
  118. May, Y. Ceramic vs. Titanium Implants | Zirconia or Titanium Implants | Dental Implant Materials. Available online: https://naturaldentistrycenter.com/zirconiaimplants/implants/ (accessed on 1 August 2023).
  119. Sharma, A.; Waddell, J.N.; Li, K.C.; Sharma, L.A.; Prior, D.J.; Duncan, W.J. Is titanium-zirconium alloy a better alternative to pure titanium for oral implant? Composition, mechanical properties, and microstructure analysis. Saudi Dent. J. 2021, 33, 546–553. [Google Scholar] [CrossRef] [PubMed]
  120. Li, J.; Li, S.J.; Hao, Y.L.; Huang, H.H.; Bai, Y.; Hao, Y.Q.; Guo, Z.; Xue, J.Q.; Yang, R. Electrochemical and surface analyses of nanostructured Ti–24Nb–4Zr–8Sn alloys in simulated body solution. Acta Biomater. 2014, 10, 2866–2875. [Google Scholar] [CrossRef] [PubMed]
  121. Khurshid, Z.; Hafeji, S.; Tekin, S.; Habib, S.R.; Ullah, R.; Sefat, F.; Zafar, M.S. 2—Titanium, zirconia, and polyetheretherketone (PEEK) as a dental implant material. In Dental Implants; Zafar, M.S., Khurshid, Z., Khan, A.S., Najeeb, S., Sefat, F., Eds.; Woodhead Publishing: Sawston, UK, 2020; pp. 5–35. [Google Scholar] [CrossRef]
  122. Sandler, J.; Werner, P.; Shaffer, M.S.P.; Demchuk, V.; Altstädt, V.; Windle, A.H. Carbon-nanofibre-reinforced poly(ether ether ketone) composites. Compos. Part A Appl. Sci. Manuf. 2002, 33, 1033–1039. [Google Scholar] [CrossRef]
  123. ISO 14801:2016; Dentistry-Implants-Dynamic loading test for endosseous dental implants. Vernier: Geneva, Switzerland, 2016.
  124. Jung, R.E.; Zembic, A.; Pjetursson, B.E.; Zwahlen, M.; Thoma, D.S. Systematic review of the survival rate and the incidence of biological, technical, and aesthetic complications of single crowns on implants reported in longitudinal studies with a mean follow-up of 5 years. Clin. Oral Implant Res. 2012, 23 (Suppl. S6), 2–21. [Google Scholar] [CrossRef] [PubMed]
  125. Jiménez-Melendo, M.; Llena-Blasco, O.; Bruguera, A.; Llena-Blasco, J.; Yáñez-Vico, R.M.; García-Calderón, M.; Vaquero-Aguilar, C.; Velázquez-Cayón, R.; Gutiérrez-Pérez, J.L.; Torres-Lagares, D. Mechanical behavior of single-layer ceramized zirconia abutments for dental implant prosthetic rehabilitation. J. Clin. Exp. Dent. 2014, 6, e485–e490. [Google Scholar] [CrossRef] [PubMed]
  126. Agustín-Panadero, R.; Serra-Pastor, B.; Roig-Vanaclocha, A.; Fons-Font, A.; Solá-Ruiz, M.F. Fracture resistance and the mode of failure produced in metal-free crowns cemented onto zirconia abutments in dental implants. PLoS ONE 2019, 14, e0220551. [Google Scholar] [CrossRef] [PubMed]
  127. de Holanda Cavalcanti Pereira, A.K.; de Oliveira Limirio, J.P.J.; Cavalcanti do Egito Vasconcelos, B.; Pellizzer, E.P.; Dantas de Moraes, S.L. Mechanical behavior of titanium and zirconia abutments at the implant-abutment interface: A systematic review. J. Prosthet. Dent. 2022. [Google Scholar] [CrossRef]
  128. Kohal, R.J.; Wolkewitz, M.; Mueller, C. Alumina-reinforced zirconia implants: Survival rate and fracture strength in a masticatory simulation trial. Clin. Oral Implant Res. 2010, 21, 1345–1352. [Google Scholar] [CrossRef]
  129. Hanes, B.; Feitosa, S.; Phasuk, K.; Levon, J.A.; Morton, D.; Lin, W.S. Fracture Resistance Behaviors of Titanium-Zirconium and Zirconia Implants. J. Prosthodont. 2022, 31, 441–446. [Google Scholar] [CrossRef]
  130. Bethke, A.; Pieralli, S.; Kohal, R.J.; Burkhardt, F.; von Stein-Lausnitz, M.; Vach, K.; Spies, B.C. Fracture Resistance of Zirconia Oral Implants In Vitro: A Systematic Review and Meta-Analysis. Materials 2020, 13, 562. [Google Scholar] [CrossRef]
  131. Spies, B.C.; Fross, A.; Adolfsson, E.; Bagegni, A.; Doerken, S.; Kohal, R.J. Stability and aging resistance of a zirconia oral implant using a carbon fiber-reinforced screw for implant-abutment connection. Dent. Mater. 2018, 34, 1585–1595. [Google Scholar] [CrossRef]
  132. Sivaraman, K.; Chopra, A.; Narayan, A.I.; Balakrishnan, D. Is zirconia a viable alternative to titanium for oral implant? A critical review. J. Prosthodont. Res. 2018, 62, 121–133. [Google Scholar] [CrossRef] [PubMed]
  133. Berglundh, T.; Abrahamsson, I.; Lang, N.P.; Lindhe, J. De novo alveolar bone formation adjacent to endosseous implants. Clin. Oral Implant Res. 2003, 14, 251–262. [Google Scholar] [CrossRef] [PubMed]
  134. Terheyden, H.; Lang, N.P.; Bierbaum, S.; Stadlinger, B. Osseointegration--communication of cells. Clin. Oral Implant Res. 2012, 23, 1127–1135. [Google Scholar] [CrossRef] [PubMed]
  135. Perrotti, V.; Iaculli, F.; Fontana, A.; Piattelli, A.; Iezzi, G. 1—Introduction to bone response to dental implant materials. In Bone Response to Dental Implant Materials; Piattelli, A., Ed.; Woodhead Publishing: Sawston, UK, 2017; pp. 1–23. [Google Scholar] [CrossRef]
  136. Koch, F.P.; Weng, D.; Krämer, S.; Biesterfeld, S.; Jahn-Eimermacher, A.; Wagner, W. Osseointegration of one-piece zirconia implants compared with a titanium implant of identical design: A histomorphometric study in the dog. Clin. Oral Implant Res. 2010, 21, 350–356. [Google Scholar] [CrossRef] [PubMed]
  137. Sadid-Zadeh, R.; Willis, J.; Forgo, G.; Haraszthy, V. Comparative analysis of biofilm formation on materials used for the fabrication of implant-supported prostheses. Braz. Dent. J. 2020, 31, 380–384. [Google Scholar] [CrossRef] [PubMed]
  138. Najeeb, S.; Mali, M.; Syed, A.U.Y.; Zafar, M.S.; Khurshid, Z.; Alwadaani, A.; Matinlinna, J.P. 21—Dental implants materials and surface treatments. In Advanced Dental Biomaterials; Khurshid, Z., Najeeb, S., Zafar, M.S., Sefat, F., Eds.; Woodhead Publishing: Sawston, UK, 2019; pp. 581–598. [Google Scholar] [CrossRef]
  139. Chokaree, P.; Poovarodom, P.; Chaijareenont, P.; Yavirach, A.; Rungsiyakull, P. Biomaterials and Clinical Applications of Customized Healing Abutment&mdash;A Narrative Review. J. Funct. Biomater. 2022, 13, 291. [Google Scholar]
  140. Wennerberg, A.; Albrektsson, T. Effects of titanium surface topography on bone integration: A systematic review. Clin. Oral Implant Res. 2009, 20 (Suppl. S4), 172–184. [Google Scholar] [CrossRef] [PubMed]
  141. Shalabi, M.M.; Gortemaker, A.; Van’t Hof, M.A.; Jansen, J.A.; Creugers, N.H. Implant surface roughness and bone healing: A systematic review. J. Dent. Res. 2006, 85, 496–500. [Google Scholar] [CrossRef]
  142. Albrektsson, T.; Wennerberg, A. Oral implant surfaces: Part 1—Review focusing on topographic and chemical properties of different surfaces and in vivo responses to them. Int. J. Prosthodont. 2004, 17, 536–543. [Google Scholar]
  143. Rohr, N.; Hoda, B.; Fischer, J. Surface Structure of Zirconia Implants: An Integrative Review Comparing Clinical Results with Preclinical and In Vitro Data. Materials 2022, 15, 3664. [Google Scholar] [CrossRef]
  144. Kurup, A.; Dhatrak, P.; Khasnis, N. Surface modification techniques of titanium and titanium alloys for biomedical dental applications: A review. Mater. Today Proc. 2021, 39, 84–90. [Google Scholar] [CrossRef]
  145. Dhatrak, P.; Shirsat, U.; Deshmukh, V. Fatigue life prediction of commercial dental implants based on biomechanical parameters: A review. IJSEIMS 2015, 3, 221–226. [Google Scholar]
  146. Granato, R.; Bonfante, E.A.; Castellano, A.; Khan, R.; Jimbo, R.; Marin, C.; Morsi, S.; Witek, L.; Coelho, P.G. Osteointegrative and microgeometric comparison between micro-blasted and alumina blasting/acid etching on grade II and V titanium alloys (Ti-6Al-4V). J. Mech. Behav. Biomed. Mater. 2019, 97, 288–295. [Google Scholar] [CrossRef] [PubMed]
  147. Souza, J.C.M.; Sordi, M.B.; Kanazawa, M.; Ravindran, S.; Henriques, B.; Silva, F.S.; Aparicio, C.; Cooper, L.F. Nano-scale modification of titanium implant surfaces to enhance osseointegration. Acta Biomater. 2019, 94, 112–131. [Google Scholar] [CrossRef] [PubMed]
  148. Yadav, A.; Yadav, R.; Gupta, A.; Baranwal, A.; Bhatnagar, A.; Singh, V. Effect of Ultraviolet Irradiation on the Osseointegration of a Titanium Alloy with Bone. Contemp. Clin. Dent. 2017, 8, 571–578. [Google Scholar] [CrossRef] [PubMed]
  149. Lang, N.P.; Karring, T. Proceedings of the First European Workshop on Periodontology; 1983 February 1–4; Quintessence: Thurgau, Switzerland; Enfield, UK, 1994. [Google Scholar]
  150. Buser, D.; Janner, S.F.M.; Wittneben, J.-G.; Brägger, U.; Ramseier, C.A.; Salvi, G.E. 10-Year Survival and Success Rates of 511 Titanium Implants with a Sandblasted and Acid-Etched Surface: A Retrospective Study in 303 Partially Edentulous Patients. Clin. Implant Dent. Relat. Res. 2012, 14, 839–851. [Google Scholar] [CrossRef] [PubMed]
  151. Borges, H.; Correia, A.R.M.; Castilho, R.M.; de Oliveira Fernandes, G.V. Zirconia Implants and Marginal Bone Loss: A Systematic Review and Meta-Analysis of Clinical Studies. Int. J. Oral Maxillofac. Implant 2020, 35, 707–720. [Google Scholar] [CrossRef] [PubMed]
  152. Haro Adánez, M.; Nishihara, H.; Att, W. A systematic review and meta-analysis on the clinical outcome of zirconia implant–restoration complex. J. Prosthodont. Res. 2018, 62, 397–406. [Google Scholar] [CrossRef]
  153. Allum, S.R.; Tomlinson, R.A.; Joshi, R. The impact of loads on standard diameter, small diameter and mini implants: A comparative laboratory study. Clin. Oral Implant Res. 2008, 19, 553–559. [Google Scholar] [CrossRef]
  154. Barter, S.; Stone, P.; Brägger, U. A pilot study to evaluate the success and survival rate of titanium-zirconium implants in partially edentulous patients: Results after 24 months of follow-up. Clin. Oral Implant Res. 2012, 23, 873–881. [Google Scholar] [CrossRef] [PubMed]
  155. Altuna, P.; Lucas-Taulé, E.; Gargallo-Albiol, J.; Figueras-Álvarez, O.; Hernández-Alfaro, F.; Nart, J. Clinical evidence on titanium-zirconium dental implants: A systematic review and meta-analysis. Int. J. Oral Maxillofac. Surg. 2016, 45, 842–850. [Google Scholar] [CrossRef] [PubMed]
  156. Makary, C.; Menhall, A.; Zammarie, C.; Lombardi, T.; Lee, S.Y.; Stacchi, C.; Park, K.B. Primary Stability Optimization by Using Fixtures with Different Thread Depth According To Bone Density: A Clinical Prospective Study on Early Loaded Implants. Materials 2019, 12, 2398. [Google Scholar] [CrossRef]
  157. Hingsammer, L.; Watzek, G.; Pommer, B. The influence of crown-to-implant ratio on marginal bone levels around splinted short dental implants: A radiological and clincial short term analysis. Clin. Implant Dent Relat. Res. 2017, 19, 1090–1098. [Google Scholar] [CrossRef] [PubMed]
  158. De Santis, D.; Cucchi, A.; Rigoni, G.; Longhi, C.; Nocini, P.F. Relationship Between Primary Stability and Crestal Bone Loss of Implants Placed with High Insertion Torque: A 3-Year Prospective Study. Int. J. Oral Maxillofac. Implant 2016, 31, 1126–1134. [Google Scholar] [CrossRef] [PubMed]
  159. Cannizzaro, G.; Leone, M.; Ferri, V.; Viola, P.; Gelpi, F.; Esposito, M. Immediate loading of single implants inserted flapless with medium or high insertion torque: A 6-month follow-up of a split-mouth randomised controlled trial. Eur. J. Oral. Implant 2012, 5, 333–342. [Google Scholar]
  160. Rossi, F.; Lang, N.P.; Ricci, E.; Ferraioli, L.; Marchetti, C.; Botticelli, D. Early loading of 6-mm-short implants with a moderately rough surface supporting single crowns—A prospective 5-year cohort study. Clin. Oral Implant Res. 2015, 26, 471–477. [Google Scholar] [CrossRef] [PubMed]
  161. Held, U.; Rohner, D.; Rothamel, D. Early loading of hydrophilic titanium implants inserted in low-mineralized (D3 and D4) bone: One year results of a prospective clinical trial. Head. Face Med. 2013, 9, 37. [Google Scholar] [CrossRef]
  162. Goiato, M.C.; dos Santos, D.M.; Santiago, J.F., Jr.; Moreno, A.; Pellizzer, E.P. Longevity of dental implants in type IV bone: A systematic review. Int. J. Oral Maxillofac. Surg. 2014, 43, 1108–1116. [Google Scholar] [CrossRef]
  163. Aldebes, A.; Al-Khanati, N.M.; Abou Nassar, J.; Kharboutly, N.A.D.; Aldamman, F. Effect of restoration material on marginal bone resorption around modified anatomic zirconia dental implants: A randomised controlled trial. Ann. Med. Surg. 2022, 80, 104313. [Google Scholar] [CrossRef]
Figure 1. Flow diagram of search procedure for this narrative review.
Figure 1. Flow diagram of search procedure for this narrative review.
Jcm 12 06924 g001
Table 1. Search strategy according to three databases (PubMed, Scopus, Embase).
Table 1. Search strategy according to three databases (PubMed, Scopus, Embase).
DatabasesSearch Strategy
PubMed/MedlineMeSH terms: (Dental Implants) AND ((Osseointegration) OR (bone–implant interface) OR (survival rate))
Text words: ((Titanium) OR (titanium implant) OR (zirconia) OR (zirconium oxide) OR (yttria-stabilized tetragonal zirconia) OR (zirconia implant) OR (ceramic implant) OR (PEEK) OR (Polyetheretherketone)) AND ((bone density) OR (bone mineral) OR (bone condition)) AND ((success rate) OR (marginal bone loss) OR (bone–implant contact) OR (removal torque) OR (osteoblasts) OR (cell proliferation) OR (bone remodeling))
Scopus(Dental implants) AND ((titanium) OR (titanium implant) OR (zirconia) OR (zirconium oxide) OR (yttria-stabilized tetragonal zirconia) OR (zirconia implant) OR (ceramic implant) OR (PEEK) OR (Polyetheretherketone)) AND ((bone density) OR (bone mineral) OR (bone condition)) AND ((osseointegration) OR (bone–implant-interface) OR (survival rate) OR (success rate) OR (marginal bone loss) OR (bone–implant contact) OR (removal torque) OR (osteoblasts) OR (cell proliferation) OR (bone remodeling))
Embase(Dental implants) AND ((titanium) OR (titanium implant) OR (zirconia) OR (zirconium oxide) OR (yttria-stabilized tetragonal zirconia) OR (zirconia implant) OR (ceramic implant) OR (PEEK) OR (Polyetheretherketone)) AND ((bone density) OR (bone mineral) OR (bone condition)) AND ((osseointegration) OR (bone–implant-interface) OR (survival rate) OR (success rate) OR (marginal bone loss) OR (bone–implant contact) OR (removal torque) OR (osteoblasts) OR (cell proliferation) OR (bone remodeling))
Table 2. Percentage of different bone densities (bone type) in different jaw areas [29].
Table 2. Percentage of different bone densities (bone type) in different jaw areas [29].
TypeAnterior Maxilla (%)Posterior Maxilla (%)Anterior Mandible (%)Posterior Mandible (%)
D10063
D225106650
D365502546
D4104031
Table 3. Hounsfield values for different substances.
Table 3. Hounsfield values for different substances.
SubstanceHounsfield Units
Air−1000
Water0
BoneCancellous+300 to +400 [37]
Cortical+500 to +1900 [37,38,39]
Anterior maxilla+600 to +700 [34,40]
Posterior maxilla+300 to +400 [34,40]
Anterior mandible+800 to +1100 [34,40]
Posterior mandible+500 to +600 [34,40]
Table 4. Elastic modulus of alveolar bone and implant materials [47,49].
Table 4. Elastic modulus of alveolar bone and implant materials [47,49].
SubstancesElastic Modulus (GPa)
Zirconia Oxide210
TiAl6V4110
CpTi (Grade IV)104.1
PEEK3.6
Carbon-reinforced PEEK18
Cortical15.85 ± 2.10
Trabecular7.95 ± 2.10
Table 7. Biological properties of implant materials.
Table 7. Biological properties of implant materials.
PropertiesTitaniumZirconiaPEEKCitation
EstheticsAcceptableSuperior to TiSuperior to Ti[117,121]
Tissue adhesionAcceptableSuperior to TiLesser or similar to Ti and Zr[117,121,136,139]
BiocompatibilityAcceptableSuperior to TiSuperior to Ti[117,121,139]
Bacterial formationModerateLesser or
similar to Ti
Least[117,121,139]
CytotoxicityModerateLower than TiLeast[121]
OsseointegrationHighSimilar to Ti
(after surface treatment)
Lesser than
Ti and Zr
[96,121,136]
Table 8. Techniques frequently used to change the topography of implant surfaces [140,143].
Table 8. Techniques frequently used to change the topography of implant surfaces [140,143].
TitaniumZirconia
SubtractiveAdditiveSubtractiveAdditive
ElectropolishingHA and other calcium phosphate coatings SandblastingAdditive sintering and slurrying
Mechanical polishingTPS surfacesSandblasting followed by acid etchingInjection molding
BlastingIon depositionLaser ablationAdditionally heat-treated
Etching
Oxidation
UV light
Table 9. Comparative information about the clinical application of dental implant materials containing titanium, zirconia, and PEEK.
Table 9. Comparative information about the clinical application of dental implant materials containing titanium, zirconia, and PEEK.
Clinical SettingsTitaniumZirconiaPEEK
Bone density
-
High-density
YesYesMaybe
-
Low-density
YesNo
(low osseointegration)
Questionable
(yes, mechanical aspect)
(no, biological aspect)
Occlusal forceNormal to highNormal High (bruxism)
Esthetic benefitsMaybeYesYes
AllergyMaybeLowLow
Table 10. Meta-analyses of clinical studies on alternative implant materials and survival rates.
Table 10. Meta-analyses of clinical studies on alternative implant materials and survival rates.
Study/YearMaterialMarginal Bone LossSurvival Rate (%)
Borges et al. 2020 [151]Zirconia0.80 mm (95% CI: 0.60 to 1.00)
at a 1-year post-loading.
71.2% at 1 year to 100% at 7.8 years.
1.01 mm (95% CI: 0.72 to 1.29)
at a 2-year post-loading
Adanez et al. 2018 [152]Zirconia0.89 mm (95% CI: 0.60 to 1.18)
at a 1-year post-loading period.
76% to 100% after observation periods between 1 and 7 years.
The mean survival rate was 95% after an observation period between 1 and 7 years (one-piece zirconia: 95%, two-piece zirconia: 94%).
Borges et al. 2020 [151]Titanium–zirconia alloy0.36 ± 0.06 mm after 1 year.98.4% at 1 year after implant placement.
0.41 ± 0.09 mm after 2 years.97.7% at 2 years after implant
placement.
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Khaohoen, A.; Sornsuwan, T.; Chaijareenont, P.; Poovarodom, P.; Rungsiyakull, C.; Rungsiyakull, P. Biomaterials and Clinical Application of Dental Implants in Relation to Bone Density—A Narrative Review. J. Clin. Med. 2023, 12, 6924. https://doi.org/10.3390/jcm12216924

AMA Style

Khaohoen A, Sornsuwan T, Chaijareenont P, Poovarodom P, Rungsiyakull C, Rungsiyakull P. Biomaterials and Clinical Application of Dental Implants in Relation to Bone Density—A Narrative Review. Journal of Clinical Medicine. 2023; 12(21):6924. https://doi.org/10.3390/jcm12216924

Chicago/Turabian Style

Khaohoen, Angkoon, Tanapon Sornsuwan, Pisaisit Chaijareenont, Pongsakorn Poovarodom, Chaiy Rungsiyakull, and Pimduen Rungsiyakull. 2023. "Biomaterials and Clinical Application of Dental Implants in Relation to Bone Density—A Narrative Review" Journal of Clinical Medicine 12, no. 21: 6924. https://doi.org/10.3390/jcm12216924

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