Next Article in Journal
Differential Expression and Clinicopathological Significance of HER2, Indoleamine 2,3-Dioxygenase and PD-L1 in Urothelial Carcinoma of the Bladder
Next Article in Special Issue
Association of Salivary Human Papillomavirus Infection and Oral and Oropharyngeal Cancer: A Meta-Analysis
Previous Article in Journal
Anemia and Systemic Inflammation Rather than Arterial Circulatory Dysfunction Predict Decompensation of Liver Cirrhosis
Previous Article in Special Issue
Salivary Biomarkers and Their Correlation with Pain and Stress in Patients with Burning Mouth Syndrome
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JCM
Volume 9
Issue 5
10.3390/jcm9051264
jcm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Salivary Levels of Titanium, Nickel, Vanadium, and Arsenic in Patients Treated with Dental Implants: A Case-Control Study

by
Piero Papi
1,
Andrea Raco
1,
Nicola Pranno
1,*,
Bianca Di Murro
1,
Pier Carmine Passarelli
2,
Antonio D’Addona
2,
Giorgio Pompa
1,† and
Maurizio Barbieri
3,†
1
Department of Oral and Maxillo-Facial Sciences, “Sapienza” University of Rome, 00161 Rome, Italy
2
Division of Oral Surgery and Implantology, Department of Head and Neck, Oral Surgery, and Implantology Unit, Institute of Clinical Dentistry, Fondazione Policlinico Universitario A. Gemelli IRCCS-Università Cattolica del Sacro Cuore, 00168 Rome, Italy
3
Department of Earth Sciences, “Sapienza” University of Rome, 00161 Rome, Italy
*
Author to whom correspondence should be addressed.
†
These two authors contributed equally.
J. Clin. Med. 2020, 9(5), 1264; https://doi.org/10.3390/jcm9051264
Submission received: 22 March 2020 / Revised: 19 April 2020 / Accepted: 23 April 2020 / Published: 27 April 2020
(This article belongs to the Special Issue Saliva and Oral Diseases)
Versions Notes

Abstract

:
Background: Recent articles have hypothesized a possible correlation between dental implants dissolution products and peri-implantitis. The null hypothesis tested in this case-control study was that there would be no differences in salivary concentrations of titanium (Ti), vanadium (V), nickel (Ni) and arsenic (As) ions among patients with dental implants, healthy (Group A) or affected by peri-implantitis (Group B), compared to subjects without implants and/or metallic prosthetic restorations (Group C). Methods: Inductively coupled plasma mass spectrometry was used to analyze saliva samples. One-way repeated-measure analysis of variance (ANOVA) was used to identify statistically significant differences in the salivary level of Ti, V, Ni and As between the three groups. Results: A total of 100 patients were enrolled in the study (42 males and 58 females), distributed in three groups: 50 patients in Group C, 26 patients in Group B and 24 patients Group B. In our study, concentrations of metallic ions were higher in Group A and B, compared to the control group, with the exception of vanadium. However, there were no statistically significant differences (p > 0.05) for metallic ions concentrations between Group A and Group B. Conclusions: Based on our results, there are no differences in titanium or other metals concentrations in saliva of patients with healthy or diseased implants.

1. Introduction

Dental implants are usually made of commercially pure titanium or titanium-based alloys (Ti-6Al-4V), these metals, as well as showing great long-term success and survival rates [1,2], are known to be bio compatibles and chemically inert in the oral cavity and consequently considered corrosion-resistant. Corrosion is a state of metal’s deterioration caused by oxidation or chemical action, thwarted by a titanium dioxide layer (TiO2), spontaneously covering the implant surface in presence of oxygen and providing great resistance and stability to the implant [3,4]. Nevertheless, titanium alloys can be affected by this gradual degradation and the structural and mechanical integrity of the implant may be jeopardized and at risk of failure. Corrosion leads to titanium dissolution, release and dispersion of metal ions and particles into soft and hard tissues either, which may be a possible factor in peri-implant inflammatory processes [5,6].
The factors that trigger corrosion are acidification of the oral environment or the release of lactic acid by bacteria, such as Streptococcus mutans, and also chemical stimuli by fluorides (with a concentration range greater than 100 ppm) normally present in home and professional oral care products [7,8,9].
Titanium and other metals particles released by dental implants are not totally bioinert: they induce the release of mediating inflammation cytokines, such as tumor necrosis factor-alpha (TNF-α), interleukin 1 beta (IL-1β) and the secretion of RANKL. These present an immunogenic potential which—by acting as a secondary inflammatory stimulus in peri-implantitis—amplifies bone resorption [10]
Under physiological conditions, osteoprotegerin (OPG) secreted by the fibroblasts of the periodontal ligament and osteoblasts, subtracts the receptor activator of nuclear factor kappa-Β ligand (RANKL) from the link with its true receptor activator of nuclear factor kappa-Β (RANK), creating a real competitive inhibition, preventing differentiation from the pre-osteoclast into osteoclasts and subsequent bone resorption [11,12]. In the presence of inflammation, an up-regulation of RANKL is associated with a down-regulation of OPG, which is produced in minimal quantities. The RANKL produced will, therefore, bind the RANK present on the osteoclastic precursors, with consequent massive bone resorption [13,14]
Furthermore, other kinds of corrosion can occur, such as mechanical corrosion due to functional stresses of implants or the cracking or weakening of its prosthetic components [7,8].
Once ultimately dispersed in the peri-implant environment, metal ions and particles are no longer biocompatible and inert, and are, therefore considered a potential incentive to the inflammatory process in peri-implantitis [5]. A study in mice immune cells has demonstrated that Titanium ions release pro-inflammatory cytokines involved in bone resorption, demonstrating that peri-implantitis may be directly related to corrosion and, therefore, with metal ions dispersion [15].
Peri-implantitis treatment and risk factors are still controversial [16,17], with incontrovertible evidence just for periodontitis, inadequate plaque control and lack of supportive periodontal therapy [18,19,20].
Furthermore, smoking, excess cement and other systemic conditions have all been described as potential risk indicators, however there is inconclusive evidence to draft clear conclusions [18,21,22,23,24,25,26].
Recent articles have hypothesized a possible correlation between titanium dissolution products and peri-implantitis [27,28,29] therefore, the aims of this case-control study were to evaluate salivary metallic ions dissolution in patients with dental implants, healthy or affected by peri-implantitis.
The null hypothesis tested was that there would be no differences in the salivary concentrations of titanium (Ti), vanadium (V), nickel (Ni) and arsenic (As) ions among patients with dental implants, healthy or affected by peri-implantitis, compared to subjects without implants and/or metallic prosthetic restorations.

2. Material and Methods

2.1. Study Design

To address the research purpose, the authors designed a case-control study, conducted at the Departments of Oral and Maxillo-Facial Sciences, at “Sapienza” University of Rome.

2.2. Study Population

From May 2018 to May 2019, all subjects who underwent previous implant surgery since January 2008 at the Oral Surgery Unit, Policlinico Umberto I, “Sapienza” University of Rome were identified and consecutively evaluated.
Each patient received detailed descriptions of the study protocol and all subjects signed an informed consent form to be included in the study population, according to the World Medical Declaration of Helsinki. The Institution Review Board of “Sapienza” approved the study (Ref. 4939/2018).
Eligible patients were divided into two groups: subjects with clinically healthy implants (Group A) and patients with peri-implantitis (Group B).
Patients in group A were enrolled in the study based on the following inclusion and exclusion criteria:
  • Single crown implants functioning for >1 year
  • No clinical signs of pathologies of the oral mucosa
  • Age ≥ 18 years
  • Implants classified as clinically healthy
  • No antibiotic treatment in the previous three months
  • Non-smoker
  • No uncontrolled systemic diseases
  • Not pregnant or breastfeeding
  • No metal reconstruction, crowns or other prosthetic restorations present in the oral cavity
Patients in Group B had to meet the following inclusion and exclusion criteria:
  • Single crown implants functioning for >1 year
  • No clinical signs of pathologies of the oral mucosa
  • Age ≥ 18 years
  • Implants with a diagnosis of peri-implantitis
  • No antibiotic treatment in the previous three months
  • Non-smoker
  • No uncontrolled systemic diseases
  • Not pregnant or breastfeeding
  • No metal reconstruction, crowns or other prosthetic restorations present in the oral cavity
Furthermore, a third group of patients (Group C) without dental implants, derived from a population of subjects attending the Oral Surgery Unit from May 2018 to May 2019 for wisdom tooth removal, was enrolled in accordance with the following inclusion and exclusion criteria:
  • Absence of dental implants
  • No metal reconstruction, crowns or other prosthetic restorations present in the oral cavity
  • Age ≥ 18 years
  • No clinical signs of pathologies of the oral mucosa
  • No antibiotic treatment in the previous three months
  • Non-smoker
  • No uncontrolled systemic diseases
  • Not pregnant or breastfeeding

2.3. Clinical Examination

Patients’ data collected included sex and age.
For each implant, the following clinical measurements were recorded at six sites per implant by using a periodontal probe (PCP-Unc 15, Hu-Friedy®, Chicago, IL, USA):
  • Probing pocket depth (PPD) measured in millimeters
  • Plaque index (PI) recorded with dichotomic values (present/absent)
  • Mucosal redness recorded with dichotomic values (present/absent)
  • Suppuration recorded with dichotomic values (present/absent)
  • Bleeding on probing recorded with dichotomic values (present/absent)

2.4. Radiographic Assessment

Mesial and distal implant crestal bone levels were measured on standardized (Rinn Centratore XCP Evolution 2003, Dentsply, Rome, Italy) digital periapical X-rays for each implant using a calibrated software (SOPRO Imaging, Acteon Group, Norwich, UK). The implant length and width were used as references for calibration of measurements, with the bone level digitally evaluated by measuring the distance between the implant shoulder and the first visible bone contact on the implant.
Case definitions for epidemiological or disease surveillance studies of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions were adopted to establish the diagnosis of peri-implant diseases [30].

2.5. Saliva Collection

Five milliliters of saliva were collected from each patient using the unstimulated drainage method, or alternatively by leaving the saliva flow passively from the lower lip directly into designated sterile tubes.
Patients were advised not to take food or drink and to avoid oral hygiene procedures before saliva collection.
All samples were stored at a temperature of 1 °C, in order to block any biologic process still in place.

2.6. ICP-MS Analysis

Samples were analyzed using a Thermo Scientific XSERIES2 ICP-MS instrument (Thermo-Fisher Scientific, Waltham, MA, USA) at the Department of Earth Sciences at “Sapienza” University of Rome. Samples were processed as previously described [29]. The concentrations of Ti, V, Ni and As were quantified in μg/L.

2.7. Statistical Analysis

The required sample size was calculated using statistics software (GPower 3.1.9.2, Heinrich-Heine-Universität, Düsseldorf, Germany). A power analysis using the repeated measures ANOVA with three measurements, an alpha level of 0.05 and a medium effect size (f = 0.56) showed that 100 subjects would be adequate to obtain 95% power in detecting a statistical difference in the salivary level of Ti, assuming a loss to follow-up of 20% [31].
A database was created using Excel (Microsoft, Redmond, WA, USA). Descriptive statistics were calculated for each variable. The Shapiro–Wilk test was used to determine whether or not the data conformed to a normal distribution.
One-way repeated-measures ANOVA was used to identify statistically significant differences in the salivary level of Ti, V, Ni and As between three different groups: Control group, patients with healthy implant and patients with implant affected by peri-implantitis. Pairwise Tukey honestly significant difference (HSD) test for multiple comparisons.
The chi-squared test of homogeneity was used to evaluate the presence of differences in the proportion of males and females among the three groups.
Data were evaluated using standard statistical analysis software (version 20.0, Statistical Package for the Social Sciences, IBM Corporation, Armonk, NY, USA). A p value <0.05 was considered as statistically significant.

3. Results

A total of 100 patients were enrolled in the study (42 males and 58 females; age 49.02 ± 11.37 years). The patients were thus distributed in the three groups: 50 patients in Group C, 26 patients in Group B and 24 patients Group B. There were no significant differences in the proportions of males and females in the three groups (p = 0.620). Patients’ demographics are reported in Table 1.

3.1. Titanium

The mean concentration of Ti was 136.65 ± 263.28 μg/L in the Group C, 489.60 ± 227.86 μg/L in the Group A and 492.83 ± 313.90 in the Group B. Statistical significant differences in mean concentration were found between the Group C and the Group A (p < 0.001) and between the Group C and the Group B (p < 0.001) (Table 2).

3.2. Nickel

The mean concentration of Ni was 4.77 ± 8.33 μg/L in the Group C, 24.99 ± 12.47 μg/L in the Group A and 23.50 ± 10.12 in the Group B. Statistical significant differences in mean concentration were found between the Group C and the Group A (p < 0.001) and between the Group C and Group B (p < 0.001) (Table 2).

3.3. Vanadium

The mean concentration of V was 1.30 ± 4.28 μg/L in the Group C, 2.27 ± 2.43 μg/L in the Group A and 2.01 ± 1.35 in the Group B. The group means of V concentration were not statistically significant different (p = 0.440) (Table 2).

3.4. Arsenic

The mean concentration of As was 0.01 ± 0.01 μg/L in the Group C, 2.20 ± 1.88 μg/L in the Group A and 1.54 ± 2.07 in the Group B. Statistical significant differences in mean concentration were found between the Group C and the Group A (p < 0.001) and between the Group C and the Group B (p < 0.001) (Table 2).

4. Discussion

The aims of this study were to detect salivary metallic ions levels of Ti, V, Ni and As in patients with and without dental implants.
The metal concentration was measured by the use of ICP-MS, a versatile, rapid and extremely sensitive analytical technique used to determine different metallic and non-metallic inorganic substances present in concentrations lower than one part per billion.
Just a few studies have investigated the possible relationship of metallic ions dissolution and peri-implantitis, mainly focusing on titanium levels [27,28,29]
Safioti et al. first hypothesized a possible association between high titanium levels and implants affected by peri-implantitis, studying the metal concentration in submucosa plaque. The plaque samples were taken from the deepest points of the pockets of each implant through dental scalers (mini-five 1–2 Gracey) and then analyzed by ICP-MS. Results showed that implants with peri-implantitis had significantly (p < 0.05) higher titanium levels than healthy implants [27].
Olmedo et al. using the exfoliative cytology technique, measured the concentration of titanium particles in the peri-implant mucosa cells and found higher values in the group of patients affected by peri-implantitis compared to the group of patients with healthy implants [28,32].
In our study setting, attention was focused not only on titanium but also on other metals such as V, Ni and As.
Vanadium is ubiquitous: it is present in water and soil and its effects at systemic level are still debated: several authors have reported the use of vanadium in the treatment of diabetes mellitus, while others have correlated the long-term exposure with risk of cancer [33,34,35,36].
Nickel is known to be the cause of contact dermatitis and in general of allergic episodes, which can develop with serious consequences in the most sensitive subjects. Adverse reactions were documented in relation to orthodontic devices (brackets, arches) containing nickel. This element has a carcinogenic and mutagenic effects; therefore, exposure must be minimized [37,38,39].
Arsenic is one of the most widespread elements in nature: it can be found in soil, water, air and almost in all animal and plant tissues.
Arsenic poisoning can be acute (lethal) or chronic, caused by prolonged exposure even at low concentrations.
Martin-Camean et al. in 2014, in an in vivo study, evaluated the dissolution of different metal ions in the oral mucosa of subjects with orthodontic mini-implants. The epithelial cells of the oral mucosa were taken from each patient using a rubber brush. The samples were then analyzed through ICP-MS. The results reported only traces of vanadium, while the release of other elements occurred in the following growing order Cr < Ni < Ti < Cu < Al [40,41,42].
In our study, concentrations of metallic ions were higher in subjects with dental implants, either healthy or affected by peri-implantitis, compared to the control group, with the exception of vanadium.
Based on our results, metallic ions are detectable in the saliva of patients with dental implants; according to a recent systematic review conducted by Noronha Oliveira et al., degradation products—in the form of micro and nanoscale particles—can be found for different reasons, such as detachment from implant surface during surgical insertion, wear caused by micro-movements between contacting surfaces at implant connections, corrosive effects of therapeutic substances, like bleaching agents and fluorides or peri-implantitis treatment (mainly implantoplasty) [43].
In the present study, there were no statistically significant differences (p > 0.05) for metallic ions concentrations between patients with healthy dental implants and peri-implantitis subjects.
Our results are in contrast with the findings of Safioti et al. and Olmedo et al. [27,28]. However, in the above-mentioned articles, exclusion criteria did not limit enrollment to patients without other metallic prosthetic reconstructions and a control group without implants was not provided.
A recent systematic review by Gomes et al. [44] evaluated the diagnostic accuracy of biomarker levels in saliva to distinguish between healthy implants and implants affected by peri-implantitis. Based on their results, there was no clear evidence to support the use of salivary biomarkers (IL-6, IL-1β) in peri-implantitis detection. Pettersson et al. [45] performed gingival biopsies during surgical treatment of patients with severe periodontitis or peri-implantitis in order to evaluate titanium levels via ICP-MS. They found higher titanium values in peri-implantitis patients (p < 0.001) compared to periodontitis subjects, however samples were obtained after surgical treatment of dental implants and titanium release may be, therefore, exacerbated by ultrasonic scaling, as previously demonstrated by Eger et al. [46].
Furthermore, human samples from appropriate control groups (healthy implants and patients without metallic reconstructions) could not be obtained for ethical reasons.
Therefore, saliva collection and analysis through ICP-MS, as performed in the present study, seem a viable alternative to investigate data obtained by different populations.

5. Conclusions

Current evidence on the possible role of titanium or other metal particles in peri-implantitis pathogenesis is still controversial: in a recent critical review, Mombelli et al. concluded that there is poor specificity for the association of titanium particles and peri-implantitis, since metallic ions can be commonly detected in healthy and diseased peri-implant mucosa, as well as in gingiva of subjects without dental implants, being Tio2 used in multiple kinds of foods, toothpastes, cosmetics or medical pills [10].
Schwarz et al. in the latest World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions [18] stated that there was insufficient available evidence to consider titanium particles as a risk indicator for peri-implantitis.
Based on our results, concentrations of metallic ions were higher in subjects with dental implants, either healthy or affected by peri-implantitis, compared to the control group, with the exception of vanadium. No statistically significant differences were found in the metallic concentrations of healthy implants or peri-implantitis.
Future research should be orientated in conducting further studies, with a larger sample and a longitudinal design, to determine the role of titanium or other metals in peri-implantitis pathogenesis.

Author Contributions

P.P. and A.R. drafted the article, revised the paper and gave substantial contributions to the conception of the work; G.P. and A.D. gave substantial contributions to the conception of the work and revised the manuscript critically for important intellectual content. N.P. revised the paper, gave substantial contributions to the conception of the work and performed the statistical analysis. B.D.M. and P.C.P. revised the paper, gave substantial contributions to the conception of the work and recruited patients. M.B. gave substantial contributions to the conception of the work, revised the manuscript critically for important intellectual content and performed the ICP-MS analysis. All authors have read and agreed to the published version of the manuscript.

Conflicts of Interest

The authors declare they have no conflicts of interest related to this study.

References

  1. De Angelis, F.; Papi, P.; Mencio, F.; Rosella, D.; Di Carlo, S.; Pompa, G. Implant survival and success rates in patients with risk factors: Results from a long-term retrospective study with a 10 to 18 years follow-up. Eur. Rev. Med. Pharmacol. Sci. 2017, 21, 433–437. [Google Scholar] [PubMed]
  2. Rossi, F.; Lang, N.P.; Ricci, E.; Ferraioli, L.; Baldi, N.; Botticelli, D. Long-term follow-up of single crowns supported by short, moderately rough implants—A prospective 10-year cohort study. Clin. Oral Implant. Res. 2018, 29, 1212–1219. [Google Scholar] [CrossRef] [PubMed]
  3. Li, J.; He, X.; Zhang, G.; Hang, R.; Huang, X.; Tang, B.; Zhang, X. Electrochemical corrosion, wear and cell behavior of ZrO(2)/TiO(2) alloyed layer on Ti-6Al-4V. Bioelectrochemistry 2018, 121, 105–114. [Google Scholar] [CrossRef]
  4. Zhang, R.; Wan, Y.; Ai, X.; Liu, Z.; Zhang, D. Corrosion resistance and biological activity of TiO(2) implant coatings produced in oxygen-rich environments. Proc. Inst. Mech. Eng. Part H 2017, 231, 20–27. [Google Scholar] [CrossRef]
  5. Delgado-Ruiz, R.; Romanos, G. Potential Causes of Titanium Particle and Ion Release in Implant Dentistry: A Systematic Review. Int. J. Mol. Sci. 2018, 19, 3585. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Apaza-Bedoya, K.; Tarce, M.; Benfatti, C.A.M.; Henriques, B.; Mathew, M.T.; Teughels, W.; Souza, J.C.M. Synergistic interactions between corrosion and wear at titanium-based dentalimplant connections: A scoping review. J. Periodontal Res. 2017, 52, 946–954. [Google Scholar] [CrossRef] [PubMed]
  7. Maruthamuthu, S.; Rajasekar, A.; Sathiyanarayanan, S.; Muthukumar, N.; Palaniswamy, N. Electrochemical behaviour of microbes on orthodontic wires. Curr. Sci. 2005, 89, 988–996. [Google Scholar]
  8. Chang, J.C.; Oshida, Y.; Gregory, R.L.; Andres, C.J.; Barco, T.M.; Brown, D.T. Electrochemical study on microbiology-related corrosion of metallic dental materials. Bio-Med. Mater. Eng. 2003, 13, 281–295. [Google Scholar]
  9. Souza, J.C.M.; Henriques, M.; Oliveira, R.; Teughels, W.; Celis, J.P.; Rocha, L.A. Do oral biofilms influence the wear and corrosion behavior of titanium titanium? Biofouling 2010, 26, 471–478. [Google Scholar] [CrossRef] [PubMed]
  10. Mombelli, A.; Hashim, D.; Cionca, N. What is the impact of titanium particles and biocorrosion on implant survival and complications? A critical review. Clin. Oral. Implant. Res. 2018, 29, 37–53. [Google Scholar] [CrossRef]
  11. Boyce, B.F.; Xing, L. Functions of RANKL/RANK/OPG in bone modeling and remodeling. Arch. Biochem. Biophys. 2008, 473, 139–146. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Walsh, M.C.; Choi, Y. Biology of the RANKL-RANK-OPG System in Immunity, Bone, and Beyond. Front. Immunol. 2014, 5, 511. [Google Scholar]
  13. Wachi, T.; Shuto, T.; Shinohara, Y.; Matono, Y.; Makihira, S. Release of titanium ions from an implant surface and their effect on cytokine production related to alveolar bone resorption. Toxicology 2015, 327, 1–9. [Google Scholar] [CrossRef] [PubMed]
  14. Cadosch, D.; Al-Mushaiqri, M.S.; Gautschi, O.P.; Meagher, J.; Simmen, H.P.; Filgueira, L. Biocorrosion and uptake of titanium by human osteoclasts. J. Biomed. Mater. Res. 2010, 95, 1004–1010. [Google Scholar] [CrossRef] [PubMed]
  15. Nishimura, K.; Kato, T.; Ito, T. Influence of titanium ions on cytokine levels of murine splenocytes stimulated with periodontopathic bacterial lipopolysaccharide. Int. J. Oral. Maxillofac. Implant. 2014, 29, 472–477. [Google Scholar]
  16. La Monaca, G.; Pranno, N.; Annibali, S.; Cristalli, M.P.; Polimeni, A. Clinical and radiographic outcomes of a surgical reconstructive approach in the treatment of peri-implantitis lesions: A 5-year prospective case series. Clin. Oral Implant. Res. 2018, 29, 1025–1037. [Google Scholar] [CrossRef]
  17. Mencio, F.; De Angelis, F.; Papi, P.; Rosella, D.; Pompa, G.; Di Carlo, S. A randomized clinical trial about presence of pathogenic microflora and risk of peri-implantitis: Comparison of two different types of implant-abutment connections. Eur. Rev. Med. Pharmacol. Sci. 2017, 21, 1443–1451. [Google Scholar]
  18. Schwarz, F.; Derks, J.; Monje, A.; Wang, H.L. Peri-implantitis. J. Periodontol. 2018, 89, 267–290. [Google Scholar] [CrossRef]
  19. Pimentel, S.P.; Shiota, R.; Cirano, F.R.; Casarin, R.C.V.; Pecorari, V.G.A.; Casati, M.Z.; Haas, A.N.; Ribeiro, F.V. Occurrence of peri-implant diseases and risk indicators at the patient and implant levels: A multilevel cross-sectional study. J. Periodontol. 2018, 89, 1091–1100. [Google Scholar] [CrossRef]
  20. Dreyer, H.; Grischke, J.; Tiede, C.; Eberhard, J.; Schweitzer, A.; Toikkanen, S.E.; Glöckner, S.; Krause, G.; Stiesch, M. Epidemiology and risk factors of peri-implantitis: A systematic review. J. Periodontal Res. 2018, 53, 657–681. [Google Scholar] [CrossRef]
  21. Papi, P.; Di Murro, B.; Pranno, N.; Bisogni, V.; Saracino, V.; Letizia, C.; Polimeni, A.; Pompa, G. Prevalence of peri-implant diseases among an Italian population of patients with metabolic syndrome: A cross-sectional study. J. Periodontol. 2019, 90, 1374–1382. [Google Scholar] [CrossRef]
  22. Papi, P.; Letizia, C.; Pilloni, A.; Petramala, L.; Saracino, V.; Rosella, D.; Pompa, G. Peri-implant diseases and metabolic syndrome components: A systematic review. Eur. Rev. Med. Pharmacol. Sci. 2018, 22, 866–875. [Google Scholar] [PubMed]
  23. Kotsakis, G.A.; Lan, C.X.; Barbosa, J.; Lill, K.; Chen, R.Q.; Rudney, J.; Aparicio, C. Antimicrobial agents used in the treatment of peri-implantitis alter the physicochemistry and cytocompatibility of titanium surfaces. J. Periodontol. 2016, 87, 809–819. [Google Scholar] [CrossRef] [PubMed]
  24. Gurgel, B.C.V.; Montenegro, S.C.L.; Dantas, P.M.C.; Pascoal, A.L.B.; Lima, K.C.; Calderon, P.D.S. Frequency of peri-implant diseases and associated factors. Clin. Oral Implant. Res. 2017, 28, 1211–1217. [Google Scholar] [CrossRef] [PubMed]
  25. Dalago, H.; Schuldt Filho, G.; Rodrigues, M.; Renvert, S.; Bianchini, M. Risk indicators for peri-implantitis: A cross-sectional study with 916 implants. Clin. Oral Implant. Res. 2017, 28, 144–150. [Google Scholar] [CrossRef] [PubMed]
  26. Renvert, S.; Aghazadeh, A.; Hallström, H.; Persson, G.R. Factors related to peri-implantitis—A retrospective study. Clin. Oral Implant. Res. 2014, 25, 522–529. [Google Scholar] [CrossRef] [PubMed]
  27. Safioti, L.M.; Kotsakis, G.A.; Pozhitkov, A.E.; Chung, W.O.; Daubert, D.M. Increased levels of dissolved titanium are associated with peri-implantitis—A cross-sectional study. J. Periodontol. 2017, 88, 436–442. [Google Scholar] [CrossRef]
  28. Olmedo, D.G.; Nalli, G.; Verdú, S.; Paparella, M.L.; Cabrini, R.L. Exfoliative cytology and titanium dental implants: A pilot study. J. Periodontol. 2013, 84, 78–83. [Google Scholar] [CrossRef]
  29. Barbieri, M.; Mencio, F.; Papi, P.; Rosella, D.; Di Carlo, S.; Valente, T.; Pompa, G. Corrosion behavior of dental implants immersed into human saliva: Preliminary results of an in vitro study. Eur. Rev. Med. Pharmacol. Sci. 2017, 21, 3543–3548. [Google Scholar]
  30. Berglundh, T.; Armitage, G.; Araujo, M.G. Peri-implant diseases and conditions: Consensus report of workgroup 4 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. J. Clin. Periodontol. 2018, 45, 286–291. [Google Scholar] [CrossRef] [Green Version]
  31. Faul, F.; Erdfelder, E.; Lang, A.G.; Buchner, A. G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav. Res. Methods 2007, 39, 175–191. [Google Scholar] [CrossRef]
  32. Olmedo, D.; Fernandez, M.M.; Guglielmotti, M.B.; Cabrini, R.L. Macrophages related to dental implant failure. Implant Dent. 2003, 12, 75–80. [Google Scholar] [CrossRef] [PubMed]
  33. Zwolak, I. Vanadium carcinogenic, immunotoxic and neurotoxic effects: A review of in vitro studies. Toxicol. Mech. Methods 2014, 24, 1–12. [Google Scholar] [CrossRef] [PubMed]
  34. Domingo, J.L.; Gómez, M. Vanadium compounds for the treatment of human diabetes mellitus: A scientific curiosity? A review of thirty years of research. Food Chem. Toxicol. 2016, 95, 137–141. [Google Scholar] [CrossRef] [PubMed]
  35. Imtiaz, M.; Rizwan, M.S.; Xiong, S.; Li, H.; Ashraf, M.; Shahzad, S.M.; Shahzad, M.; Rizwan, M.; Tu, S. Vanadium, recent advancements and research prospects: A review. Environ. Int. 2015, 80, 79–88. [Google Scholar] [CrossRef] [PubMed]
  36. Gruzewska, K.; Michno, A.; Pawelczyk, T.; Belarczyk, H. Essentiality and toxicity of vanadium supplements in health and pathology. J. Physiol. Pharmacol. 2014, 65, 603–611. [Google Scholar]
  37. Lu, L.; Vollmer, J.; Moulon, C.; Weltzien, H.U.; Marrack, P.; Kappler, J. Components of the ligand for a Ni++ reactive human T cell clone. J. Exp. Med. 2003, 197, 567–574. [Google Scholar] [CrossRef] [Green Version]
  38. Saito, M.; Arakaki, R.; Yamada, A.; Tsunematsu, T.; Kudo, Y.; Ishimaru, N. Molecular mechanisms of nickel allergy. Int. J. Mol. Sci. 2016, 17, 202. [Google Scholar] [CrossRef] [Green Version]
  39. Girolomoni, G.; Gisondi, P.; Ottaviani, C.; Cavani, A. Immunoregulation of allergic contact dermatitis. J. Dermatol. 2004, 31, 264–270. [Google Scholar] [CrossRef]
  40. Martín-Cameán, A.; Jos, A.; Calleja, A.; Gil, F.; Iglesias, A.; Solano, E.; Cameán, A.M. Validation of a method to quantify titanium, vanadium and zirconium in oral mucosa cells by inductively coupled plasma-mass spectrometry (ICP-MS). Talanta 2014, 118, 238–244. [Google Scholar] [CrossRef]
  41. Martín-Cameán, A.; Jos, A.; Puerto, M.; Calleja, A.; Iglesias-Linares, A.; Solano, E.; Cameán, A.M. In vivo determination of aluminum, cobalt, chromium, copper, nickel, titanium and vanadium in oral mucosa cells from orthodontic patients with mini-implants by inductively coupled plasma-mass spectrometry (ICP-MS). J. Trace Elem. Med. Biol. 2015, 32, 13–20. [Google Scholar] [CrossRef] [PubMed]
  42. Martín-Cameán, A.; Molina-Villalba, I.; Jos, A.; Iglesias-Linares, A.; Solano, E.; Cameán, A.M.; Gil, F. Biomonitorization of chromium, copper, iron, manganese and nickel in scalp hair from orthodontic patients by atomic absorption spectrometry. Environ. Toxicol. Pharmacol. 2014, 37, 759–771. [Google Scholar] [CrossRef] [PubMed]
  43. Noronha Oliveira, M.; Schunemann, W.V.H.; Mathew, M.T.; Henriques, B.; Magini, R.S.; Teughels, W.; Souza, J.C.M. Can degradation products released from dental implants affect peri-implant tissues? J. Periodontal Res. 2018, 53, 1–11. [Google Scholar] [CrossRef] [PubMed]
  44. Gomes, A.M.; Douglas-de-Oliveira, D.W.; Oliveira Costa, F. Could the biomarker levels in saliva help distinguish between healthy implants and implants with peri-implant disease? A systematic review. Arch. Oral Biol. 2018, 96, 216–222. [Google Scholar] [CrossRef]
  45. Pettersson, M.; Pettersson, J.; Johansson, A.; Molin Thorén, M. Titanium release in peri-implantitis. J. Oral Rehabil. 2019, 46, 179–188. [Google Scholar] [CrossRef] [PubMed]
  46. Eger, M.; Sterer, N.; Liron, T.; Kohavi, D.; Gabet, Y. Scaling of titanium implants entrains inflammation-induced osteolysis. Sci. Rep. 2017, 7, 39612. [Google Scholar] [CrossRef]
Table
Table 1. Sample demographic.
Table 1. Sample demographic.
Study VariableGroup AGroup BGroup C
Sample size262450
Male111120
Female151330
Age (y) ± SD (range)63.13 ± 17.7270.52 ± 8.2446.57 ± 9.23
Dental implants (n)2624NA
Functional loading (y) ± SD (range)7.8 ± 2.629.88 ± 3.52NA
Mean PPD (mm)3.2 ± 0.444.66 ± 1.32NA
Mean MBL (mm)0.89 ± 0.321.95 ± 1.43NA
SD, standard deviation; PPD, probing pocket depth; MBL, marginal bone loss; NA, not applicable.
Table
Table 2. Difference in the mean concentration of titanium, nickel vanadium and arsenic in the three groups.
Table 2. Difference in the mean concentration of titanium, nickel vanadium and arsenic in the three groups.
Multiple Comparisons
Tukey’s HSD
Dependent Variable(I) Groups(J) GroupsMean Difference (I-J)Std. ErrorSig.95% Confidence Interval
Lower BoundUpper Bound
TitaniumGroup CGroup A−352.951280 *59.5172720.000−494.61555−211.28701
Group B−356.184613 *61.1270070.000−501.68041−210.68882
Group AGroup C352.951280 *59.5172720.000211.28701494.61555
Group B−3.23333369.6787910.999−169.08426162.61760
Group BGroup C356.184613 *61.1270070.000210.68882501.68041
Group A3.23333369.6787910.999−162.61760169.08426
NickelGroup CGroup A−20.215246 *2.4108870.000−25.95369−14.47680
Group B−18.728483 *2.4760930.000−24.62213−12.83483
Group AGroup C20.215246 *2.4108870.00014.4768025.95369
Group B1.4867632.8225030.858−5.231428.20494
Group BGroup C18.728483 *2.4760930.00012.8348324.62213
Group A−1.4867632.8225030.858−8.204945.23142
VanadiumGroup CGroup A−0.9655290.8093200.460−2.891890.96083
Group B−0.7072600.8312090.672−2.685721.27120
Group AGroup C0.9655290.8093200.460−0.960832.89189
Group B0.2582690.9474970.960−1.996982.51352
Group BGroup C0.7072600.8312090.672−1.271202.68572
Group A−0.2582690.9474970.960−2.513521.99698
ArsenicGroup CGroup A−2.193412 *0.3362860.000−2.99385−1.39298
Group B−1.525553 *0.3453820.000−2.34764−0.70347
Group AGroup C2.193412 *0.3362860.0001.392982.99385
Group B0.6678590.3937010.212−0.269241.60496
Group BGroup C1.525553 *0.3453820.0000.703472.34764
Group A−0.6678590.3937010.212−1.604960.26924
* The mean difference is significant at the 0.05 level. HSD, honestly significant difference.

Share and Cite

MDPI and ACS Style

Papi, P.; Raco, A.; Pranno, N.; Di Murro, B.; Passarelli, P.C.; D’Addona, A.; Pompa, G.; Barbieri, M. Salivary Levels of Titanium, Nickel, Vanadium, and Arsenic in Patients Treated with Dental Implants: A Case-Control Study. J. Clin. Med. 2020, 9, 1264. https://doi.org/10.3390/jcm9051264

AMA Style

Papi P, Raco A, Pranno N, Di Murro B, Passarelli PC, D’Addona A, Pompa G, Barbieri M. Salivary Levels of Titanium, Nickel, Vanadium, and Arsenic in Patients Treated with Dental Implants: A Case-Control Study. Journal of Clinical Medicine. 2020; 9(5):1264. https://doi.org/10.3390/jcm9051264

Chicago/Turabian Style

Papi, Piero, Andrea Raco, Nicola Pranno, Bianca Di Murro, Pier Carmine Passarelli, Antonio D’Addona, Giorgio Pompa, and Maurizio Barbieri. 2020. "Salivary Levels of Titanium, Nickel, Vanadium, and Arsenic in Patients Treated with Dental Implants: A Case-Control Study" Journal of Clinical Medicine 9, no. 5: 1264. https://doi.org/10.3390/jcm9051264

APA Style

Papi, P., Raco, A., Pranno, N., Di Murro, B., Passarelli, P. C., D’Addona, A., Pompa, G., & Barbieri, M. (2020). Salivary Levels of Titanium, Nickel, Vanadium, and Arsenic in Patients Treated with Dental Implants: A Case-Control Study. Journal of Clinical Medicine, 9(5), 1264. https://doi.org/10.3390/jcm9051264

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop