Next Article in Journal
Characteristics, Outcomes, and Factors Affecting Mortality in Hospitalized Patients with CAP Due to Different Variants of SARS-CoV-2 and Non-COVID-19 CAP
Previous Article in Journal
Special Issue “Recent Advances in Neonatal Sepsis”
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Frequency of Smoking and Marginal Bone Loss around Dental Implants: A Retrospective Matched-Control Study

by
Amir Ali
1,†,
Ammar Al Attar
1,† and
Bruno Ramos Chrcanovic
2,*
1
Faculty of Odontology, Malmö University, 214 21 Malmö, Sweden
2
Department of Prosthodontics, Faculty of Odontology, Malmö University, 214 21 Malmö, Sweden
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
J. Clin. Med. 2023, 12(4), 1386; https://doi.org/10.3390/jcm12041386
Submission received: 30 December 2022 / Revised: 30 January 2023 / Accepted: 8 February 2023 / Published: 9 February 2023
(This article belongs to the Section Dentistry, Oral Surgery and Oral Medicine)

Abstract

:
This dental record-based retrospective study aimed to compare the marginal bone loss (MBL) around dental implants in a group of smokers in relation to a matched group of non-smokers, with a special focus on five different frequencies of daily smoking (non-smokers, and frequency of 1–5, 6–10, 11–15, and 20 cig./day). Only implants with a minimum of 36 months of radiological follow-up were considered. Univariate linear regression models were used to compare MBL over time between 12 clinical covariates, after which a linear mixed-effects model was built. After matching of the patients, the study included 340 implants in 104 smokers, and 337 implants in 100 non-smokers. The results suggested that smoking degree (greater MBL for higher degrees of smoking), bruxism (greater MBL for bruxers), jaw (greater MBL in maxilla), prosthesis fixation (greater MBL for screw-retained prosthesis), and implant diameter (greater MBL for 3.75–4.10 mm) had a significant influence on MBL over time. There appears to be a positive correlation between the degree of smoking and the degree of MBL, meaning, the higher the degree of smoking, the greater the MBL. However, the difference is not apparent for different degrees of smoking when this is high, namely above 10 cigarettes per day.

1. Introduction

The estimated number of smokers in the world at the year of 2019 was 1.1 billion people. Since 1990, the prevalence of smokers has fallen because of the growth population, but the number of smokers has increased. Smoking is a harmful habit and causes around 8 million deaths each year [1].
In addition to many serious illnesses, such as cancer, stroke, cardiovascular diseases, and other health problems, smoking cigarettes has a huge impact on oral health [2]. In addition to raising the risk of periodontal disease, smoking cigarettes is linked to poor oral health [3]. Cigarette smoking has an impact on increased tooth mobility [4] and there is a greater risk of tooth loss among smokers than among non-smokers [5,6]. Smoking has also been associated with a higher risk of dental implant failure and a worse effect on the level of marginal bone around implants in comparison to non-smokers [7,8].
A relationship seems to exist between frequency of smoking and periodontal disease. Heavy smoking was found to have high prevalence and severity of periodontitis as compared with moderate and light smokers [9].
When it comes to dental implants, studies have compared marginal bone loss (MBL) between groups of smokers and non-smokers concerning some further sub-groups, such as turned vs. oxidized implants [10], periodontally healthy vs. periodontally compromised patients [11], different prosthetic configurations of implant-supported overdentures in the mandible [12], diabetic vs. non-diabetic patients [13], and immediate and delayed loading [14]. For the great majority of the cases, smoking resulted in greater MBL than in non-smokers, regardless of these aforementioned sub-divisions. A recent review on the effect of smoking on dental implants included 292 studies, of which 32 provided information comparing the mean MBL between smokers and non-smokers [8]. Taking together the results of these 32 studies, it was observed that implants placed in smokers presented a statistically significant mean 0.580 mm higher MBL than the implants placed in non-smokers. As each and every one of these 32 studies provided clear information on MBL between these two groups, a simple dichotomous analysis on MBL between smokers and non-smokers would not present any novelty. It is not clear, however, how the varying frequency of daily smoking would affect marginal bone loss (MBL) around dental implants.
Therefore, the aim of the present retrospective study was to compare the MBL around dental implants in a group of smoker patients in relation to a matched group of non-smokers, taking into consideration several variables, with a special focus on different frequencies of daily smoking. Patients in this study were classified into five groups according to the different frequencies of daily smoking.

2. Materials and Methods

2.1. Research Question

The focused question was elaborated by using the PICO format (Participants, Interventions, Comparisons, Outcomes): “Do smokers undergoing implant-prosthetic rehabilitation present a higher MBL in comparison to non-smokers?”
The null hypothesis was that there would be no difference in MBL between smokers, different frequencies of smoking, and non-smokers, against the alternative hypothesis of a difference.

2.2. Materials

This retrospective study included patients treated with dental implants during the period 1980–2018 at one specialist clinic (Clinic for Prosthodontics, Centre of Dental Specialist Care, Malmö, Sweden). This study was based on data collection from patients’ dental records. The implants were placed by specialist dentists in oral surgery, and dentists performing the prosthetic treatment were specialists in prosthodontics.
The study was approved by the regional Ethical Committee, Lund, Sweden (Dnr 2014/598; Dnr 2015/72). The present retrospective study followed the STROBE guidelines for observational studies and was registered at https://clinicaltrials.gov under the registration number NCT02369562, last updated on 3 May 2019.

2.3. Definitions

For this study, patients smoking a minimum of one cigarette per day (an everyday smoker [15]) were classified as smokers, established at the clinical appointment of the patient when the anamnesis was performed.
MBL was defined as loss, in an apical direction, of alveolar bone marginally adjacent to the dental implant, in relation to the marginal bone level initially detected after the implant was surgically placed [16].
The diagnosis of bruxism was established in a previous study [17], in which the patients of the aforementioned database suspected to be bruxers were called back for one clinical appointment to get the minimum information in order to diagnose the patients as ‘probable bruxers’ (self-report/anamnesis + clinical examination).
As the standard protocol in the clinic, the patients’ dental hygiene was followed up by a dental hygienist within 6 months after the final implant-supported/retained restoration. Each patient then attended a dental hygiene recall program based on individual needs.

2.4. Inclusion and Exclusion Criteria

Only implants that did not present loss of osseointegration and with baseline radiographs taken within 12 months after implant placement and with a minimum of 36 months of radiological follow-up were considered for the analysis of MBL. Negative values of MBL correspond to bone loss.
Patients with all modern types of threaded implants with cylindrical or conical design were included. Zygomatic implants were not included in the study, nor were implants detected in radiographies but lacking basic information about them in the patients’ files.
Patients were excluded if they had a history of periodontitis and/or were treated for periodontal disease. It is important to take note that as standard, all patients receiving implants at the Specialist Clinic for Prosthodontics were periodontally healthy at the time of implant installation. Patients with either a history or signs of periodontal disease were treated at the Specialist Clinic for Periodontology, where they later could or not receive dental implants, according to individual needs/indications. These patients were not included in the present study.

2.5. Data Collection

The data were directly entered into a SPSS file (SPSS software, version 28, SPSS Inc., Chicago, IL, USA) as the dental records of the patients were being read, and it consisted of the following variables: patient age at implant installation, patient’s sex, probable bruxism (yes/no), diabetes status (absent, type 1, type 2), smoking habit (yes/no), number of cigarettes/day (frequency of 0 [non-smoker], 1–5, 6–10, 11–15, and 20 cigarettes per day), implant location (regarding jaw [maxilla/mandible, anterior/posterior—anterior region comprised incisors and canines] and tooth region [incisor, canine, premolar, molar]), implant diameter (three groups: 3.00–3.50, 3.75–4.10, and 4.30–5.00 mm), implant surface (turned/machined, modified), prosthesis type (single crown, fixed dental prosthesis (FDP) of 2 to 6 prosthetic units, FDP of 7 to 10 units, full-arch, overdenture), prosthesis fixation (cemented, screwed), and follow-up time.

2.6. Formation of a Matched Group

Since the division of all initial patients into groups would generate extremely unbalanced groups and the variance was not homogenous between them, the two groups were therefore not expected to be comparable with respect to important covariates [18], and then methods were used to match patients and implants between smokers to non-smokers patients. Matching minimizes the chance that any differences between the study and the control groups are a result of differences on the matching variables, thus reducing selection bias.
The matching was performed using the ‘case control matching’ function in SPSS, and the matches were selected based on similarities in (a) patient’s age at the time of the surgery, (b) number of implants, and (c) total radiological follow-up time. As there were no perfect matches in a first matching attempt considering all three variables, some tolerance was set for the predictors: ±5 years for the patient’s age, ±2 implants, and ±12 months for the total radiological follow-up time. Thus, a little variance of these predictors between the groups was expected.

2.7. Marginal Bone Level Evaluation

The evaluation of the variation of the marginal bone level over time was performed according to a previous study [19]. Reproducible intra-oral radiographs were used. When there were no available digital radiographies from the baseline appointment, the analogue periapical radiographies were scanned at 1200 dpi (Epson Perfection V800 Photo Color Scanner; Nagano, Japan). Marginal bone level (MBL) was measured after calibration based on the inter-thread distance of the implants. Information about the inter-thread distance was obtained from the implant catalogue of each implant manufacturer. Measurements were taken from the implant-abutment junction to the marginal bone level, at both mesial and distal sides of each implant, and then the mean value of these two measurements was considered. MBL was calculated by comparing bone-to-implant contact levels to the radiographic baseline examination. The Image J software (National Institute of Health, Bethesda, MD, USA) was used for all measurements.
The sets of radiographs for every patient were codified, and the authors who performed the radiological measurements (A.A., A.A.A.) were blinded to the smoking habit for every patient.

2.8. Calibration

An initial calibration concerning MBL was performed between the authors. The process was done for 10 random samples from the cohort group and verified after the measurement of each sample. At the end of the process, the measurements from the different individuals were considered approximate enough to each other, with agreement between examiners set at >80% of the distance in millimeters.

2.9. Sample Size Calculation

The calculation of the sample size was based on the results of a study [20], which observed a mean MBL ± SD for smokers of 0.57 ± 0.93 mm, and 0.30 ± 0.58 mm for non-smokers. There was a need for 186 implants in each group having set alpha (α) at 0.05 and power at 80%. The sample size calculation was performed with ClinCalc.com.

2.10. Statistical Analyses

The mean, standard deviation, and percentages were presented as descriptive statistics. The Kolmogorov–Smirnov test was performed to evaluate the normal distribution of the variables, and Levene’s test evaluated homoscedasticity. The performed tests for two independent groups were Student’s t-test or the Mann–Whitney test, and paired-samples t-test or Wilcoxon signed-rank test for two dependent groups, depending on the normality. Pearson’s chi-squared test or Fisher’s exact test was used in the analysis of contingency tables of categorical data of independent groups, and McNemar’s test for dependent groups.
Univariate linear regression models were used to compare MBL over time between clinical covariates. The estimation of MBL over time (dependent variable) was expressed in a single linear regression equation for each of the categories of each independent variable (smoking, diabetes, bruxism, sex, age, jaw, jaw region, tooth region, implant diameter, implant surface, prosthesis type, prosthesis fixation). For the present study, the linear regression equation was expressed as y = b + ax, where ‘y’ is the estimated MBL over time, ‘b’ is the estimated intercept at the y-axle in the scatter plot, ‘a’ is the estimated MBL per each one month of follow-up, and ‘x’ is the number of months of follow-up. Thus, if one would like to estimate the MBL of a certain category of a certain variable at, for example, 100 months of follow-up, ‘x’ is replaced by the value of 100 in the equation given for that particular category and variable.
In order to verify multicollinearity, a correlation matrix of all of the predictor variables was scanned, to see whether there were some high correlations among the predictors. Collinearity statistics obtaining variance inflation factor (VIF) and tolerance statistic were also performed to detect more subtle forms of multicollinearity. A linear mixed-effects model was built with all variables that were moderately associated (p < 0.10) with MBL in the univariate linear regression models. A mixed-effects model was used in order to take into consideration that some patients had more than one implant-supported prosthesis, as multiple observations within an individual are not independent of each other. Multiple testing corrections for p-values were performed by the Bonferroni adjustment.
The degree of statistical significance was considered p < 0.05. Data were statistically analyzed using the Statistical Package for the Social Sciences (SPSS) version 28 software (SPSS Inc., Chicago, IL, USA).

3. Results

The cohort group initially included 760 implants installed in 210 patients, 105 smokers and 105 non-smokers. The periapical radiographs for one smoker and five non-smoker patients were excluded for not being of sufficient quality. Therefore, 204 patients were included in the present study (104 smokers, 100 non-smokers), with 677 dental implants (340 in smokers, 337 in non-smokers). Most of the implants of the study were Brånemark MK implants (Nobel Biocare, Göteborg, Sweden), totaling 590 implants (382 turned/machined and 208 TiUnite implants).
The mean age (±SD) of the 204 patients was 54.6 ± 14.7 years (min–max, 15.2–81.3) at the day of the implant surgical placement. The patients were followed up clinically for a mean (±SD) of 162.4 ± 75.6 months (min–max, 40.4–364.2), and radiographically for a mean (±SD) of 133.1 ± 75.0 months (min–max, 39.6–364.2).
Table 1 shows the descriptive data of the implants included in the study. The variable patient’s age was divided into three categories each, based on the 33.3 and 66.7 percentiles of sample distribution, in order to generate groups of more balanced sample sizes. There was a difference in distribution of implants of different surfaces between the groups, as well as for the age groups of the patients, and the distribution of patients with different types of diabetes. The site of 20 implants were submitted to augmentation procedure simultaneous to implant placement, and 12 implant sites were submitted to autogenous graft varying from 4.7 to 10 months previous to the implant placement surgery.
The total number of marginal bone level double measurements (mesial + distal sides of each implant) was 4324. Table 2 shows data on MBL distributed by different periods of follow-up, separated by different frequencies of daily smoking. The general picture was an increase in MBL with time of follow-up and with the frequency of smoking. It is important to stress that not all implants in all patients were followed up for the same period of time.
Analysis of the univariate linear regression analysis (Table 3) showed that the estimated MBL over time was statistically significantly different between the categories of the following variables: smoking degree (greater MBL for higher degrees of smoking) (Figure 1); bruxism (greater MBL for bruxers) (Figure 2); patient’s sex (greater MBL in men); patient’s age at the time of implant placement (greater MBL for the range 51–61 years); jaw (greater MBL in maxilla); jaw region (greater MBL in posterior region); implant diameter (greater MBL for regular diameter implants); implant surface (greater MBL for implants with modified surface); prosthesis type (greater MBL for FDP 2–6 units and full-arch fixed prosthesis); and prosthesis fixation (greater MBL for screw-retained prosthesis). Most the categories had a moderate degree of linear correlation (R2 linear) with MBL over time. Diabetes and tooth region were not statistically significant.
The results of the linear mixed-effects model (Table 4) suggested that smoking degree (greater MBL for higher degrees of smoking), bruxism (greater MBL for bruxers), jaw (greater MBL in maxilla), implant diameter (greater MBL for regular diameter implants), and prosthesis fixation (greater MBL for screw-retained prosthesis) had a statistically significant influence on MBL over time.

4. Discussion

The aim of the present retrospective study was to investigate the influence of smoking on MBL at dental implants. According to the results of the present study, there was a statistically significant difference in MBL between smokers and non-smokers. Therefore, the null hypothesis was rejected. Some factors may explain these results.
Much is believed to be associated with the negative effects of the smoking toxins on bone metabolism and osteogenesis, and on angiogenesis. Cigarette smoke exposure results in the reduction of the bone trabeculae thickness which is associated with a decrease in mineralizing surface as well as in the mineral deposition rate [21]. Cigarette smoke also disturbs angiogenesis by inhibiting several biochemical and physiological processes that results in abnormal blood supply to tissues, which in turn decreases repair of damaged tissues and remodeling [22]. There is an increased risk of peri-implantitis in smokers compared to non-smokers [23]. Systematic reviews with meta-analysis on the subject including 107 and 292 studies, respectively, suggested that smoking has a worse effect on the level of marginal bone around implants in comparison to non-smokers [7,8].
The results of the present study suggest that there appears to be a positive correlation between the degree of smoking and the degree of MBL. A study suggested that smoking lowers bone mineral density and is a result of decreased calcium absorption associated with secondary hyperparathyroidism and increased bone resorption. Moreover, a significant increase in bone remodeling markers was observed in heavy smokers in comparison to light smokers, suggesting that the negative effect of smoking on bone may be higher with an increase in smoking frequency [24]. The results of a study showed that individuals smoking up to 10 cigarettes a day presented similar MBL to non-smokers [25]. However, this study had mean follow-up of less than four years and investigated a very limited number of implants, with a considerable unbalance between the number of implants in smokers versus non-smokers. Many studies that investigated the possible effect of smoking on MBL around implants failed to report the level of smoking of the included smoker individuals [8]. Even when this information is provided, there is a lack of homogeneity of what would be considered a ‘light smoker’ and a ‘heavy smoker’. The positive correlation between the degree of smoking and the degree of MBL in the present study was more clearly observed up to a certain limit, and patients who used to smoke between 11 and 20 cigarettes per day showed similar estimated MBL over time. This might suggest that the deleterious effects of smoking on MBL may not significantly increase after an already high degree of smoking. However, more studies are necessary in order to verify whether the negative effect of smoking on the marginal bone levels may tend to level above a certain degree of cigarette smoking.
The impact of smoking on MBL may also be associated with the duration of smoking, although this was not investigated in the present study. Cigarette smoking contributes to the constriction and damage of arteries, and promotes endothelial dysfunction and by altering lipoprotein metabolism, coagulation, and platelet function [26]. Some studies showed that the effect of cumulative smoking exposure on arterial damage has a dose–response relationship [27,28]. It is likely that the nocive effects of smoking are cumulative also on bone [29]. The cumulative negative effect of pack-years of smoking might have a significant negative effect on MBL as well, as the long-term maintenance of normal bone metabolism and vascular health may play an important role in the maintenance of bone around dental implants.
The greater MBL in bruxers in relation to non-bruxers could be associated with the absence of a periodontal ligament around dental implants, limiting the amount of feedback the central nervous system receives, causing a reduction in the tactile sensitivity around implants [30]. Therefore implant-supported restorations are more likely to be subjected to higher loads during bruxism because of this reduced tactile sensitivity around implants [31,32,33,34], which could in theory negatively affect the marginal bone level. The results of the first clinical study comparing MBL in a group of bruxers in relation to a matched group of non-bruxers suggested that bruxism increases the risk of MBL over time [19]. The fact that a patient had an occlusal splint was not a reliable piece of information, as confirmed in the study that previously investigated the bruxers in this cohort [17]. There were cases where patients had an occlusal splint but were used only eventually, or used only during the first two weeks, or never used it.
There was an estimated greater MBL over time around implants in the maxilla in comparison to implants in the mandible. This could be related to the differences in bone quality between the jaws [35]. Smoking may be a significant risk factor with adverse effects on implants in areas of loose trabecular bone but may not be as significant for dense bone sites, such as the mandible [36].
Another finding was the greater estimated MBL over time for regular diameter implants in comparison to narrow and wide diameter implants. This goes against the results of a study that observed greater MBL with larger diameter implants [37] and could be related to the extremely unbalanced groups of implants of different diameter ranges. The authors of this previous study [37] hypothesized that the posterior regions of the jaw more often present an alveolar ridge wide enough to receive wide implants, in a region where tissue architecture is different and mechanical loads are higher. According to them, larger implants are therefore expected to be subjected to higher compressive forces, and these may have caused more resorption.
The last factor to show a statistically significant difference in the estimated MBL over time was the prosthesis fixation type, with screw-retained, implant-supported restoration showing greater MBL than around implants supporting cemented restorations. In vitro and in vivo studies have suggested that there is minimal stress exertion on the implant and the crestal bone around it with cement-retained prostheses in comparison to screw-retained prostheses [38,39,40]. However, we cannot draw any conclusions from this, since a disproportionate amount of screw-retained and cement-retained implant-supported prostheses were used for this retrospective study. There should be a study dedicated to this subject that accounts for both types of anchoring prostheses to the implant.
As limitations of the present study, this was a dental record-based retrospective study. The nature of a retrospective study inherently results in flaws. These problems were manifested by the gaps in information and incomplete records. Furthermore, all data rely on the accuracy of the original examination and documentation. Items may have been excluded in the initial examination or not recorded in the dental chart. Moreover, the smoking habit was assessed at the time of implant installation and might have changed over time for each patient.

5. Conclusions

Smoking negatively affect the MBL at implants. There appears to be a positive correlation between the degree of smoking and the degree of MBL, meaning, the higher the degree of smoking, the greater the MBL. However, this correlation is more clearly observed up to a certain limit. The difference is not apparent for different degrees of smoking when this is high, namely above 10 cigarettes per day.
Other factors that are suggested to negatively affect MBL are bruxism, implant location (in the maxilla), implant diameter (greater MBL for 3.75 mm–4.10 mm), and screwed implant-supported prostheses.

Author Contributions

Conceptualization, B.R.C.; methodology, B.R.C.; investigation, A.A., A.A.A. and B.R.C.; writing—original draft, A.A., A.A.A. and B.R.C.; data curation, B.R.C.; formal analysis, B.R.C.; writing—review and editing, A.A., A.A.A. and B.R.C.; visualization, B.R.C.; supervision, B.R.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Folktandvården Skåne AB, Sweden.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the regional Ethical Committee, Lund, Sweden (Dnr 2014/598; Dnr 2015/72).

Informed Consent Statement

As a record-based retrospective study, informed consent was not required for the present study.

Data Availability Statement

Restrictions apply to the availability of these data. Data were obtained from patients treated at Folktandvården Skåne AB, Malmö, Sweden, and cannot be shared, in accordance with the General Data Protection Regulation (EU) 2016/679.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. GBD 2019 Tobacco Collaborators. Spatial, temporal, and demographic patterns in prevalence of smoking tobacco use and attributable disease burden in 204 countries and territories, 1990-2019: A systematic analysis from the Global Burden of Disease Study 2019. Lancet 2021, 397, 2337–2360. [Google Scholar] [CrossRef] [PubMed]
  2. Wald, N.J.; Hackshaw, A.K. Cigarette smoking: An epidemiological overview. Br. Med. Bull. 1996, 52, 3–11. [Google Scholar] [CrossRef] [PubMed]
  3. Haas, R.; Haimböck, W.; Mailath, G.; Watzek, G. The relationship of smoking on peri-implant tissue: A retrospective study. J. Prosthet. Dent. 1996, 76, 592–596. [Google Scholar] [CrossRef] [PubMed]
  4. Worthington, H.; Clarkson, J.; Davies, R. Extraction of teeth over 5 years in regularly attending adults. Community Dent. Oral Epidemiol. 1999, 27, 187–194. [Google Scholar] [CrossRef]
  5. Ragnarsson, E.; Elíasson, S.T.; Olafsson, S.H. Tobacco smoking, a factor in tooth loss in Reykjavík, Iceland. Scand. J. Dent. Res. 1992, 100, 322–326. [Google Scholar] [CrossRef]
  6. Yoshida, Y.; Hatanaka, Y.; Imaki, M.; Ogawa, Y.; Miyatani, S.; Tanada, S. Epidemiological study on improving the QOL and oral conditions of the aged—Part 2: Relationship between tooth loss and lifestyle factors for adults men. J. Physiol. Anthropol. Appl. Human Sci. 2001, 20, 369–373. [Google Scholar] [CrossRef]
  7. Chrcanovic, B.R.; Albrektsson, T.; Wennerberg, A. Smoking and dental implants: A systematic review and meta-analysis. J. Dent. 2015, 43, 487–498. [Google Scholar] [CrossRef]
  8. Mustapha, A.D.; Salame, Z.; Chrcanovic, B.R. Smoking and Dental Implants: A Systematic Review and Meta-Analysis. Medicina 2021, 58, 39. [Google Scholar] [CrossRef]
  9. Khan, S.; Khalid, T.; Awan, K.H. Chronic periodontitis and smoking. Prevalence and dose-response relationship. Saudi Med. J. 2016, 37, 889–894. [Google Scholar] [CrossRef]
  10. Sayardoust, S.; Gröndahl, K.; Johansson, E.; Thomsen, P.; Slotte, C. Implant survival and marginal bone loss at turned and oxidized implants in periodontitis-susceptible smokers and never-smokers: A retrospective, clinical, radiographic case-control study. J. Periodontol. 2013, 84, 1775–1782. [Google Scholar] [CrossRef]
  11. Rasperini, G.; Siciliano, V.I.; Cafiero, C.; Salvi, G.E.; Blasi, A.; Aglietta, M. Crestal bone changes at teeth and implants in periodontally healthy and periodontally compromised patients. A 10-year comparative case-series study. J. Periodontol. 2014, 85, e152–e159. [Google Scholar] [CrossRef] [PubMed]
  12. Stoker, G.; van Waas, R.; Wismeijer, D. Long-term outcomes of three types of implant-supported mandibular overdentures in smokers. Clin. Oral Implants Res. 2012, 23, 925–929. [Google Scholar] [CrossRef] [PubMed]
  13. Alqahtani, F.; Alqhtani, N.; Alkhtani, F.; Devang Divakar, D.; Al-Kheraif, A.A.; Javed, F. Clinicoradiographic markers of peri-implantitis in cigarette-smokers and never-smokers with type 2 diabetes mellitus at 7-years follow-up. J. Periodontol. 2020, 91, 1132–1138. [Google Scholar] [CrossRef] [PubMed]
  14. Al Amri, M.D.; Kellesarian, S.V.; Abduljabbar, T.S.; Al Rifaiy, M.Q.; Al Baker, A.M.; Al-Kheraif, A.A. Comparison of Peri-Implant Soft Tissue Parameters and Crestal Bone Loss Around Immediately Loaded and Delayed Loaded Implants in Smokers and Non-Smokers: 5-Year Follow-Up Results. J. Periodontol. 2017, 88, 3–9. [Google Scholar] [CrossRef] [PubMed]
  15. CDC. Centers for Disease Control and Prevention, National Center for Health Statistics, Adult Tobacco Use Information, Glossary. Available online: https://www.cdc.gov/nchs/nhis/tobacco/tobacco_glossary.htm (accessed on 1 October 2021).
  16. Albrektsson, T.; Chrcanovic, B.; Östman, P.O.; Sennerby, L. Initial and long-term crestal bone responses to modern dental implants. Periodontology 2000 2017, 73, 41–50. [Google Scholar] [CrossRef]
  17. Chrcanovic, B.R.; Kisch, J.; Albrektsson, T.; Wennerberg, A. Bruxism and dental implant treatment complications: A retrospective comparative study of 98 bruxer patients and a matched group. Clin. Oral Implants Res. 2017, 28, e1–e9. [Google Scholar] [CrossRef]
  18. D’Agostino, R.B., Jr. Propensity score methods for bias reduction in the comparison of a treatment to a non-randomized control group. Stat. Med. 1998, 17, 2265–2281. [Google Scholar] [CrossRef]
  19. Bredberg, C.; Vu, C.; Häggman-Henrikson, B.; Chrcanovic, B.R. Marginal bone loss around dental implants: Comparison between matched groups of bruxer and non-bruxer patients: A retrospective case-control study. Clin. Implant Dent. Relat. Res. 2023, 25, 124–132. [Google Scholar] [CrossRef]
  20. Vervaeke, S.; Collaert, B.; Cosyn, J.; Deschepper, E.; De Bruyn, H. A multifactorial analysis to identify predictors of implant failure and peri-implant bone loss. Clin. Implant Dent. Relat. Res. 2015, 17 (Suppl. S1), e298–e307. [Google Scholar] [CrossRef]
  21. Barbosa, A.P.; Lourenço, J.D.; Junqueira, J.J.M.; Larissa Emidio de França, S.; Martins, J.S.; Oliveira Junior, M.C.; Begalli, I.; Velosa, A.P.P.; Olivo, C.R.; Bastos, T.B.; et al. The deleterious effects of smoking in bone mineralization and fibrillar matrix composition. Life Sci. 2020, 241, 117132. [Google Scholar] [CrossRef]
  22. Ejaz, S.; Lim, C.W. Toxicological overview of cigarette smoking on angiogenesis. Environ. Toxicol. Pharmacol. 2005, 20, 335–344. [Google Scholar] [CrossRef] [PubMed]
  23. Heitz-Mayfield, L.J.; Huynh-Ba, G. History of treated periodontitis and smoking as risks for implant therapy. Int. J. Oral Maxillofac. Implants 2009, 24, 39–68. [Google Scholar] [PubMed]
  24. Rapuri, P.B.; Gallagher, J.C.; Balhorn, K.E.; Ryschon, K.L. Smoking and bone metabolism in elderly women. Bone 2000, 27, 429–436. [Google Scholar] [CrossRef] [PubMed]
  25. Kolerman, R.; Mijiritsky, E.; Barnea, E.; Dabaja, A.; Nissan, J.; Tal, H. Esthetic Assessment of Implants Placed into Fresh Extraction Sockets for Single-Tooth Replacements Using a Flapless Approach. Clin. Implant Dent. Relat. Res. 2017, 19, 351–364. [Google Scholar] [CrossRef]
  26. Lu, J.T.; Creager, M.A. The relationship of cigarette smoking to peripheral arterial disease. Rev. Cardiovasc. Med. 2004, 5, 189–193. [Google Scholar]
  27. Cui, R.; Iso, H.; Yamagishi, K.; Tanigawa, T.; Imano, H.; Ohira, T.; Kitamura, A.; Sato, S.; Shimamoto, T. Relationship of smoking and smoking cessation with ankle-to-arm blood pressure index in elderly Japanese men. Eur. J. Cardiovasc. Prev. Rehabil. 2006, 13, 243–248. [Google Scholar] [CrossRef]
  28. Lee, Y.H.; Shin, M.H.; Kweon, S.S.; Choi, J.S.; Rhee, J.A.; Ahn, H.R.; Yun, W.J.; Ryu, S.Y.; Kim, B.H.; Nam, H.S.; et al. Cumulative smoking exposure, duration of smoking cessation, and peripheral arterial disease in middle-aged and older Korean men. BMC Public Health 2011, 11, 94. [Google Scholar] [CrossRef]
  29. Ward, K.D.; Klesges, R.C. A meta-analysis of the effects of cigarette smoking on bone mineral density. Calcif. Tissue Int. 2001, 68, 259–270. [Google Scholar] [CrossRef]
  30. Meyer, G.; Fanghanel, J.; Proff, P. Morphofunctional aspects of dental implants. Ann. Anat. 2012, 194, 190–194. [Google Scholar] [CrossRef]
  31. Chrcanovic, B.R.; Albrektsson, T.; Wennerberg, A. Bruxism and Dental Implants: A Meta-Analysis. Implant Dent. 2015, 24, 505–516. [Google Scholar] [CrossRef]
  32. Chrcanovic, B.R.; Kisch, J.; Albrektsson, T.; Wennerberg, A. Bruxism and dental implant failures: A multilevel mixed effects parametric survival analysis approach. J. Oral Rehabil. 2016, 43, 813–823. [Google Scholar] [CrossRef] [PubMed]
  33. Lobbezoo, F.; Brouwers, J.E.; Cune, M.S.; Naeije, M. Dental implants in patients with bruxing habits. J. Oral Rehabil. 2006, 33, 152–159. [Google Scholar] [CrossRef] [PubMed]
  34. Mishra, S.K.; Chowdhary, R.; Chrcanovic, B.R.; Brånemark, P.I. Osseoperception in Dental Implants: A Systematic Review. J. Prosthodont. 2016, 25, 185–195. [Google Scholar] [CrossRef] [PubMed]
  35. Chrcanovic, B.R.; Albrektsson, T.; Wennerberg, A. Bone Quality and Quantity and Dental Implant Failure: A Systematic Review and Meta-analysis. Int. J. Prosthodont. 2017, 30, 219–237. [Google Scholar] [CrossRef]
  36. Klokkevold, P.R.; Han, T.J. How do smoking, diabetes, and periodontitis affect outcomes of implant treatment? Int. J. Oral Maxillofac. Implants 2007, 22, 173–202. [Google Scholar]
  37. Negri, M.; Galli, C.; Smerieri, A.; Macaluso, G.M.; Manfredi, E.; Ghiacci, G.; Toffoli, A.; Bonanini, M.; Lumetti, S. The effect of age, gender, and insertion site on marginal bone loss around endosseous implants: Results from a 3-year trial with premium implant system. Biomed. Res. Int. 2014, 2014, 369051. [Google Scholar] [CrossRef]
  38. Guichet, D.L.; Caputo, A.A.; Choi, H.; Sorensen, J.A. Passivity of fit and marginal opening in screw- or cement-retained implant fixed partial denture designs. Int. J. Oral Maxillofac. Implants 2000, 15, 239–246. [Google Scholar]
  39. Karl, M.; Taylor, T.D.; Wichmann, M.G.; Heckmann, S.M. In vivo stress behavior in cemented and screw-retained five-unit implant FPDs. J. Prosthodont. 2006, 15, 20–24. [Google Scholar] [CrossRef]
  40. Tonella, B.P.; Pellizzer, E.P.; Ferraço, R.; Falcón-Antenucci, R.M.; Carvalho, P.S.; Goiato, M.C. Photoelastic analysis of cemented or screwed implant-supported prostheses with different prosthetic connections. J. Oral Implantol. 2011, 37, 401–410. [Google Scholar] [CrossRef]
Figure 1. Scatter plot comparing the marginal bone level over time between implants placed in patients with different degrees of smoking (linear regression).
Figure 1. Scatter plot comparing the marginal bone level over time between implants placed in patients with different degrees of smoking (linear regression).
Jcm 12 01386 g001
Figure 2. Scatter plot comparing the marginal bone level over time between implants placed in bruxers and non-bruxer patients (linear regression).
Figure 2. Scatter plot comparing the marginal bone level over time between implants placed in bruxers and non-bruxer patients (linear regression).
Jcm 12 01386 g002
Table 1. Descriptive data of the implants included in the study, separated by group. The statistical unit is the implant, not the patient.
Table 1. Descriptive data of the implants included in the study, separated by group. The statistical unit is the implant, not the patient.
FactorSmokers, Implants (%)Non-Smokers, Implants (%)p Value
Follow-up a (months)
 (mean ± SD)128.8 ± 77.1139.4 ± 72.40.056 b
Age
 (mean ± SD)53.0 ± 14.256.3 ± 15.10.063 b
Sex
 Male151 (44.8)168 (49.4)0.230 c
 Female186 (55.2)172 (50.6)
Age (years)
 <50125 (37.1)100 (29.4)0.023 c
 51–61112 (33.2)107 (31.5)
 >62100 (29.7)133 (39.1)
Jaw
 Maxilla187 (55.5)182 (53.5)0.609 c
 Mandible150 (44.5)158 (46.5)
Jaw region
 Anterior191 (56.7)204 (60.0)0.380 c
 Posterior146 (43.3)136 (40.0)
Tooth region
 Incisor132 (39.2)128 (37.6)0.190 c
 Canine60 (17.8)76 (22.4)
 Premolar120 (35.6)102 (30.0)
 Molar25 (7.4)34 (10.0)
Implant diameter
 3.00–3.50 mm30 (8.9)25 (7.3)0.441 c
 3.75–4.10 mm301 (89.3)312 (91.8)
 4.30–5.00 mm6 (1.8)3 (0.9)
Implant surface
 Turned154 (45.7)228 (67.1)<0.001 c
 Modified183 (54.3)112 (32.9)
Prosthesis type b
 Single crown44 (13.1)44 (12.9)0.181 c
 FDP 2–6 units115 (34.1)102 (30.0)
 FDP 7–10 units10 (3.0)16 (4.7)
 Full-arch168 (49.8)174 (51.2)
 Overdenture0 (0)4 (1.2)
Prosthesis fixation b
 Cemented31 (9.3)37 (11.3)0.412 c
 Screwed301 (90.7)291 (88.7)
Bruxism d
 No292 (89.8)312 (93.4)0.098 c
 Yes33 (10.2)22 (6.6)
Diabetes d
 No288 (88.1)309 (91.2)<0.001 c
 Type 10 (0)13 (3.8)
 Type 239 (11.9)17 (5.0)
a Radiological follow-up; b Wilcoxon signed-rank test; c comparison of the distribution of implants, among the categories of each factor, between smokers and non-smokers; d for the cases with available information. SD—standard deviation. FDP—fixed dental prosthesis.
Table 2. Data on marginal bone loss distributed by different periods of follow-up, separated by different frequencies of daily smoking. Values in millimeters. Negative values correspond to bone loss.
Table 2. Data on marginal bone loss distributed by different periods of follow-up, separated by different frequencies of daily smoking. Values in millimeters. Negative values correspond to bone loss.
Follow-Up (Years)Non-Smoker1–5 Cig/Day6–10 Cig/Day11–15 Cig/Day20 Cig/Day
mean ± SD (min, max)
0–1−0.02 ± 0.11
(−0.97, −0.02)
−0.07 ± 0.15
(−0.83, 0.11)
−0.10 ± 0.17
(−0.80, 0.28)
−0.13 ± 0.19
(−0.76, 0.33)
−0.16 ± 0.25
(−1.00, 0.25)
1–3−0.26 ± 0.28
(−1.13, 0.46)
−0.39 ± 1.19
(−0.88, 0.01)
−0.62 ± 0.35
(−1.48, 0.00)
−0.74 ± 0.36
(−1.70, 0.00)
−0.96 ± 0.35
(−2.15, −0.23)
3–5−0.39 ± 0.30
(−1.36, 0.49)
−0.63 ± 0.23
(−1.16, −0.24)
−0.76 ± 0.35
(−1.84, 0.00)
−1.16 ± 0.49
(−2.84, −0.34)
−1.62 ± 0.60
(−2.86, −0.46)
5–10−0.56 ± 0.45
(−3.44, 0.54)
−0.84 ± 0.38
(−1.85, 0.02)
−1.32 ± 0.20
(−3.98, 0.20)
−1.70 ± 0.66
(−4.20, −0.51)
−2.15 ± 0.70
(−3.76, −0.60)
10–15−0.82 ± 0.59
(−2.87, 0.49)
−1.09 ± 0.27
(−1.65, −0.84)
−1.39 ± 0.44
(−2.58, −0.40)
−2.16 ± 0.69
(−4.10, −0.29)
−2.83 ± 0.76
(−4.58, −1.15)
15–30−0.87 ± 0.62
(−2.53, 0.25)
−1.42 ± 0.38
(−1.88, −1.01)
−2.51 ± 0.90
(−4.73, −1.14)
−2.65 ± 0.48
(−3.49, −1.33)
−3.50 ± 0.71
(−5.06, −2.01)
Table 3. Univariate linear regression analysis for MBL.
Table 3. Univariate linear regression analysis for MBL.
FactorLinear Equation *p Value aR2 Linear
Smoking
 Noy = −0.11 − 0.00411x<0.0010.358
 1–5 cig/dayy = −0.13 − 0.00693x 0.647
 6–10 cig/dayy = −0.20 − 0.01000x 0.648
 11–15 cig/dayy = −0.31 − 0.01000x 0.678
 20 cig/dayy = −0.59 − 0.01000x 0.699
Diabetes
 Noy = −0.19 − 0.00796x0.1750.412
 Type 1y = −0.08 − 0.01000x 0.866
 Type 2y = −0.35 − 0.01000x 0.447
Bruxism b
 Noy = −0.20 − 0.00773x<0.0010.388
 Yesy = −0.20 − 0.01000x 0.676
Sex
 Maley = −0.19 − 0.00848x<0.0010.388
 Femaley = −0.21 − 0.00808x 0.418
Age (years)
 <50y = −0.27 − 0.00798x<0.0010.438
 51–61y = −0.21 − 0.00896x 0.440
 >62y = −0.19 − 0.00569x 0.212
Jaw
 Maxillay = −0.21 − 0.00828x<0.0010.348
 Mandibley = −0.19 − 0.00819x 0.456
Jaw region
 Anteriory = −0.23 − 0.00816x0.0480.356
 Posteriory = −0.17 − 0.00827x 0.485
Tooth region
 Incisory = −0.23 − 0.00876x0.2450.381
 Caniney = −0.24 − 0.00708x 0.311
 Premolary = −0.16 − 0.00875x 0.500
 Molary = −0.19 − 0.00691x 0.467
Implant diameter
 3.00–3.50 mmy = −0.23 − 0.00391x0.0020.190
 3.75–4.10 mmy = −0.20 − 0.00853x 0.429
 4.30–5.00 mmy = −0.49 − 0.00342x 0.100
Implant surface
 Turnedy = −0.19 − 0.00812x<0.0010.422
 Modifiedy = −0.20 − 0.00875x 0.361
Prosthesis type
 Single crowny = −0.25 − 0.00653x<0.0010.290
 FDP 2–6 unitsy = −0.19 − 0.00828x 0.493
 FDP 7–10 unitsy = −0.25 − 0.00576x 0.363
 Full-archy = −0.21 − 0.00867x 0.388
 Overdenturey = 0.08 + 0.00349x 0.631
Prosthesis fixation b
 Cementedy = −0.25 − 0.00653x<0.0010.307
 Screwedy = −0.21 − 0.00818x 0.407
* For the linear equation, “x” represents the number of months; a comparison of the slope of the equation (variation of MBL in mm in time) between groups; b for the cases with available information.
Table 4. Linear mixed-effects model for MBL.
Table 4. Linear mixed-effects model for MBL.
Predictor VariablesF Statisticp Value
Smoking118.725<0.001
Bruxism7.2160.007
Sex2.1180.103
Age3.2450.075
Jaw23.786<0.001
Jaw region0.0720.788
Implant diameter4.9970.037
Implant surface3.5760.068
Prosthesis type0.1050.705
Prosthesis fixation6.3290.012
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Ali, A.; Al Attar, A.; Chrcanovic, B.R. Frequency of Smoking and Marginal Bone Loss around Dental Implants: A Retrospective Matched-Control Study. J. Clin. Med. 2023, 12, 1386. https://doi.org/10.3390/jcm12041386

AMA Style

Ali A, Al Attar A, Chrcanovic BR. Frequency of Smoking and Marginal Bone Loss around Dental Implants: A Retrospective Matched-Control Study. Journal of Clinical Medicine. 2023; 12(4):1386. https://doi.org/10.3390/jcm12041386

Chicago/Turabian Style

Ali, Amir, Ammar Al Attar, and Bruno Ramos Chrcanovic. 2023. "Frequency of Smoking and Marginal Bone Loss around Dental Implants: A Retrospective Matched-Control Study" Journal of Clinical Medicine 12, no. 4: 1386. https://doi.org/10.3390/jcm12041386

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