Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2022 Nov 21;25(1):124–132. doi: 10.1111/cid.13161

Marginal bone loss around dental implants: comparison between matched groups of bruxer and non‐bruxer patients: A retrospective case–control study

Clara Bredberg 1, Camila Vu 1, Birgitta Häggman‐Henrikson 2, Bruno Ramos Chrcanovic 3,
PMCID: PMC10099792  PMID: 36411179

Abstract

Purpose

To compare marginal bone loss (MBL) around dental implants in a group of bruxers in relation to a matched group of non‐bruxers.

Methods

The present record‐based retrospective study included patients selected from individuals treated with dental implants at one specialist clinic in Malmö. Only implants not lost 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 inclusion. Univariate linear regression models and a linear mixed‐effects model were performed.

Results

Two hundred and four patients (104 bruxers, 100 non‐bruxers), with a total of 811 implants (416 in bruxers, 395 in non‐bruxers) were included in the study. The results of the linear mixed‐effects model suggested that bruxism, smoking, age, region of the jaws, implant diameter, and prosthesis type had a statistically significant influence on MBL over time. Individuals who are both bruxers and smokers showed greater MBL when compared to individuals who are either a bruxer or smoker, or neither (p < 0.001).

Conclusions

Bruxism is suggested to increase the risk of MBL over time, as well as higher age, smoking, and the combination of bruxism and smoking. Other factors that showed a correlation with increased MBL were implant diameter, region of the jaws, and prosthesis type, but it is not possible to draw robust conclusions for these factors, as the categories of these variables were very unbalanced.

Keywords: bruxism, dental implants, marginal bone loss, retrospective clinical study


What is known

Some studies have suggested that mechanical stresses exceeding the biological load‐bearing capacity of a dental implant could be associated with marginal bone loss (MBL), but clinical studies comparing MBL between bruxers and non‐bruxers are still lacking.

What this study adds

This study is the first one to compare marginal bone loss around implants in matched groups of bruxer and non‐bruxer patients. The results suggest that bruxism negatively affects the marginal bone level around implants over time. The combination of bruxism and smoking results in an even worse outcome.

1. INTRODUCTION

Bruxism is generally defined as excessive grinding of teeth or jaw clenching, during sleep or wakefulness, and is considered as a parafunctional activity. The condition has been reported to occur in about 8% of adults, although some claim that it is even more prevalent, occurring in 31.4% of adults. 1 The importance of the condition is based on the fact that bruxism has been associated with many negative consequences, such as excessive mechanical tooth wear, 2 prosthodontic technical complications, 3 , 4 temporomandibular disorders, 5 headache, 6 , 7 and orofacial pain, 8 among others.

Regarding dental implants, clinical studies suggest that bruxism may be associated with higher prevalence of technical complications and failures of implant‐supported prostheses, 9 , 10 , 11 , 12 , 13 , 14 , 15 higher implant failure rate, 16 , 17 and even an increased risk of implant fracture. 18 Regarding marginal bone loss (MBL) around implants, the literature is scarce when it comes to bruxism. Some studies 19 , 20 , 21 have suggested that mechanical stresses exceeding the biological load‐bearing capacity of a dental implant could be associated with MBL. Some animal studies have suggested that excessive occlusal load on dental implants does not cause significant changes in their radiological outcomes, 22 , 23 whereas another study suggested that bone resorption around implants could be caused by excess occlusal trauma, even when there is no inflammation in the peri‐implant tissue. 24 The results of another animal experimental study suggest that excessive dynamic loads may cause crater‐like bone defects lateral to osseointegrated implants, in comparison to static‐loaded implants. 25 Additionally, it was suggested that excessive lateral static load may negatively affect the behavior of peri‐implant bone around immediately restored implants. 26 However, besides the excessive occlusal load, these animal studies did not really simulate the complexity of the parafunctional activity resulting from bruxism. Furthermore, clinical studies comparing MBL between bruxers and non‐bruxers in humans are still lacking.

Therefore, it was the aim of the present retrospective study to analyze the MBL around dental implants in a group of patients presenting bruxism in comparison with a matched group of non‐bruxers.

2. MATERIALS AND METHODS

2.1. Research question and hypothesis

The focused question was elaborated by using the PICO format (Participants, Interventions, Comparisons, Outcomes): “Do bruxers undergoing implant‐prosthetic rehabilitation present a higher MBL over time in comparison to patients not presenting bruxism?”

The null hypothesis was that there would be no difference in MBL between bruxers and non‐bruxers, against the alternative hypothesis of a difference.

2.2. Patients

This retrospective study included patients treated by certified oral surgeons and prosthodontists with dental implants and implant‐supported prostheses 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 study was approved by the regional Ethical Committee, Lund, Sweden (Dnr 2014/598; Dnr 2015/72), and was registered at the Registry of Clinical Trials (https://clinicaltrials.gov) under the registration number NCT02369562.

2.3. Definitions

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.

For this study, the authors followed the definition of bruxism proposed by Lobbezoo and colleagues 27 : “repetitive masticatory muscle activity characterized by clenching or grinding of the teeth and/or by bracing or thrusting of the mandible and specified as either sleep bruxism or awake bruxism”. The signs and symptoms of bruxism were listed according to the International Classification of Sleep Disorders, 28 following the same guidelines used in a recent study. 12 The patients suspected to be bruxers, as diagnosed in the records, were recalled in this previous study in order to be clinically re‐assessed. The clinical examination included evaluation of the presence of masticatory muscle hypertrophy, indentations on the tongue or lip and/or a linea alba on the inner cheek, damage to the dental hard tissues (e.g., cracked teeth), repetitive failures of restorative work/prosthodontic constructions, or mechanical wear of the teeth (i.e., attrition). 27 Moreover, the self‐conscience of the condition was evaluated with five questions, according to suggestions from a previous study. 29 A diagnostic grading system of ‘possible’, ‘probable’ and ‘definite’ sleep or awake bruxism was used, as suggested for clinical and research purposes. 30 The patients from a present study 12 were eligible for the present study and classified as ‘probable’ sleep or awake bruxers, based on anamnesis/self‐report together with the clinical examination.

2.4. Inclusion and exclusion criteria

All patients diagnosed as ‘probable bruxers’ were included. Only implants in situ 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 inclusion. Negative values of MBL corresponded to bone loss.

Only modern types of threaded implants with cylindrical or conical designs were included. Zygomatic implants and implants detected in radiographs, but without basic information registered in the patients' records, were not included in the study.

Patients were excluded if they presented a recent history of periodontitis. 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.

2.5. Data collection

The data were directly entered into an SPSS file (SPSS software, version 28, SPSS Inc., Chicago, Illinois) as the records of the patients were being read, and it consisted of the following variables: patient age at implant installation, patient sex, probable bruxism (yes/no), smoking habit (yes/no), number of cigarettes/day, implant location (jaw and tooth region), 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) with 2 to 6 prosthetic units, FDP with 7 to 10 units, full‐arch prosthesis, overdenture), prosthesis fixation type (cemented, screwed), prosthesis material (metal acrylic, metal ceramic, full ceramic, zirconia, acrylic).

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 (bruxers and non‐bruxers) were not expected to be comparable with respect to important covariates, 31 and methods to match patients and implants between bruxer to non‐bruxer patients were used. Matching ensures that any differences between the study and the control groups are not a result of differences in 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 (a) patient sex, (b) patient age at the time of the surgery, (c) number of implants, and (d) total radiological follow‐up time. As there were no perfect matches in a first matching attempt for all four variables, some tolerance was set for three of the predictors: ±7 years for the age of the patient, ±12 months for the total radiological follow‐up time, and ±2 for the number of implants. Thus, some variance of these predictors between the groups was expected. Moreover, as the matching was performed at the patient‐level, and as there was some tolerance for the number of implants in the matching, some variance of the variables at the implant‐level between the groups (bruxers, non‐bruxers) was also expected.

2.7. Marginal bone level evaluation

Only periapical radiographs were considered for the study. The process of periapical radiograph acquisition at the clinic is standardized, using the long cone paralleling technique. When there were no available digital radiographs from the baseline appointment, analogue periapical radiographs were scanned at 1200 dpi (Epson Perfection V800 Photo Color Scanner; Nagano, Japan). Marginal bone level was measured after calibration, based on the inter‐thread distance of the implants. 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 subsequent bone‐to‐implant contact levels to the radiographic baseline examination. The Image J software (National Institute of Health, Bethesda) was used for all measurements.

The sets of radiographs for every patient were coded and the authors who performed the radiological measurements (C.V., C.B.) were blinded to the diagnosis of the condition for every patient.

2.8. Calibration

An initial calibration concerning marginal bone level 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 enough approximate from each other, with an agreement between examiners set at >80% of the distance in millimeters.

2.9. Sample size calculation

Calculation of the sample size was not conducted. The reason was that the database from which the eligible cases for the present study were originated had a certain number of patients and dental implants, approximately 2800 and 11 000 respectively, and it would not possible to recruit more cases, as the database already included all patients treated with dental implants during the aforementioned period at the specialist clinic.

Instead, all the bruxer patients were initially considered eligible for inclusion, in order to get the maximum number of cases available, namely, the largest sample size possible from this database, provided that these cases would fulfill the inclusion criteria, that is, baseline radiographs taken within 12 months after implant placement and with a minimum of 36 months of radiological follow‐up. The number of implants in the bruxer patients was then matched to a group of non‐bruxer patients.

2.10. Statistical analyses

The mean, standard deviation, and percentages were presented as descriptive statistics. 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 Mann–Whitney test, and for three or more independent groups were ANOVA or Kruskal‐Wallis test, depending on the normality. Paired t‐test or Wilcoxon Signed Rank test was used to compare the mean value difference of continuous variables between dependent groups. 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 was used for dependent groups.

Univariate linear regression models were used to compare MBL over time between the clinical covariates. In order to verify multicollinearity, a correlation matrix of all predictor variables was scanned, to verify 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. 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.

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, Illinois).

The present retrospective study followed the STROBE guidelines for observational studies.

3. RESULTS

There were 106 patients diagnosed as probable bruxers in the cohort group, with baseline radiographs taken within 12 months after implant placement and radiographs with a minimum of 36 months of radiological follow‐up. These 106 bruxers were matched to 106 patients known not to be bruxers, and fulfilling the same radiological inclusion criteria. The periapical radiographs for two bruxers (1.9% of this group) and six non‐bruxer (5.7%) patients were excluded for not being of sufficient quality. Therefore, 204 patients were included in the present study (104 bruxers, 100 non‐bruxers), with 811 dental implants (416 in bruxers, 395 in non‐bruxers).

The mean age (±SD) of the 204 patients was 56.1 ± 14.5 years (min–max, 16.9–89.1) on the day of implant placement. The patients were followed up clinically for a mean (±SD) of 159.4 ± 81.8 months (min–max, 38.7–381.8), and radiographically for a mean (±SD) of 127.4 ± 76.3 months (min–max, 36.4–363.0).

Table 1 shows the descriptive data of the cases included in the study, separated by group. The variable of 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.

TABLE 1.

Descriptive data of the implants included in the study, separated by group. The statistical unit is the implant, not the patient.

Factor Bruxers Implants (%) Non‐bruxers Implants (%) p value
Follow‐up (months)
(mean ± SD) 165.5 ± 82.8 153.1 ± 80.3 0.079 a
Age
(mean ± SD) 55.1 ± 15.1 57.1 ± 13.8 0.216 a
Age (years)
≤52 145 (34.9) 122 (30.9) 0.001 b
52.1–63.9 152 (36.5) 111 (28.1)
≥64 119 (28.6) 162 (41.0)
Sex
Male 234 (56.2) 247 (62.5) 0.069b
Female 182 (43.8) 148 (37.5)
Jaw
Maxilla 265 (63.7) 225 (57.0) 0.050b
Mandible 151 (36.3) 170 (43.0)
Region
Incisive 118 (28.4) 141 (35.7) 0.027 b
Canine 74 (17.8) 81 (20.5)
Premolar 177 (42.5) 143 (36.2)
Molar 47 (11.3) 30 (7.6)
Implant surface
Turned 227 (54.6) 201 (50.9) 0.294 b
Modified 189 (45.4) 194 (49.1)
Implant diameter
3.00–3.50 mm 34 (8.2) 16 (4.1) 0.033 b
3.75–4.10 mm 371 (89.2) 371 (94.2)
4.30–5.00 mm 11 (2.6) 7 (1.8)
Prosthesis type
Single crown 59 (12.1) 49 (12.4) 0.003
FDP 2–6 units 160 (38.7) 110 (27.8)
FDP 7–10 units 13 (3.2) 26 (6.6)
Full‐arch 185 (44.8) 208 (52.7)
Overdenture 5 (1.2) 2 (0.5)
Prosthesis fixation c
Cemented 39 (9.5) 32 (8.2) 0.515b
Screwed 373 (90.5) 360 (91.8)
Prosthesis material c
Metal acrylic 189 (45.9) 223 (57.2) 0.014 b
Metal ceramic 188 (45.6) 135 (34.6)
Full ceramic 15 (3.6) 17 (4.4)
Zirconia 15 (3.6) 13 (3.3)
Acrylic 5 (1.2) 2 (0.5)
Smoking c
No 223 (64.3) 277 (72.1) 0.022 b
Yes d 124 (35.7) 107 (27.9)

Abbreviations: FDP, fixed dental prosthesis; SD, standard deviation.

a

Wilcoxon Signed Rank test.

b

Comparison of the distribution of cases, among the categories of each factor, between bruxers and non‐bruxers.

c

For the cases with available information.

d

It includes 48 implants in 9 former smokers.

The total number of marginal bone level double measurements (mesial and distal sides of each implant) was 4823, with 2569 double measurements in bruxers and 2254 in non‐bruxers. The univariate linear regression analysis showed that the mean loss of marginal bone over time was statistically significantly different between the categories of all variables (Table 2). The scatter plot with a comparison of MBL over time between bruxers and non‐bruxers is presented (Figure 1). As the superimposition of dots in the scatter plot can give the false impression that most implants in non‐bruxers presented only good results, scatter plots with data separated for non‐bruxers (Figure 2) and for bruxers (Figure 3) are also presented.

TABLE 2.

Univariate linear regression analysis for MBL

Factor Linear equation a p value b R 2 linear
Bruxism
No y = −0.35 − 0.00546x <0.001 0.146
Yes y = −0.49 − 0.01000x 0.417
Smoking c
No y = −0.38 − 0.00795x <0.001 0.251
Yes d y = −0.54 − 0.00889x 0.314
Age (years)
≤52 y = −0.49 − 0.00769x <0.001 0.322
52.1–63.9 y = −0.37 − 0.00924x 0.280
≥64 y = −0.37 − 0.00972x 0.239
Sex
Male y = −0.45 − 0.00804x <0.001 0.245
Female y = −0.39 − 0.00943x 0.353
Jaw
Maxilla y = −0.45 − 0.00762x <0.001 0.223
Mandible y = −0.37 − 0.00997x 0.389
Region
Incisive y = −0.40 − 0.00922x <0.001 0.319
Canine y = −0.39 − 0.00777x 0.238
Premolar y = −0.43 − 0.00836x 0.269
Molar y = −0.45 − 0.00934x 0.361
Implant surface
Turned y = −0.42 − 0.00773x <0.001 0.296
Modified y = −0.31 − 0.01000x 0.326
Implant diameter
3.00–3.50 mm y = −0.32 − 0.01000x <0.001 0.243
3.75–4.10 mm y = −0.41 − 0.00850x 0.299
4.30–5.00 mm y = −0.40 − 0.02000x 0.497
Prosthesis type
Single crown y = −0.39 − 0.01000x <0.001 0.302
FDP 2–6 units y = −0.42 − 0.00952x 0.324
FDP 7–10 units y = −0.33 − 0.00874x 0.354
Full‐arch y = −0.40 − 0.00778x 0.260
Overdenture y = −0.34 − 0.01000x 0.789
Prosthesis fixation c
Cemented y = −0.32 − 0.01000x <0.001 0.406
Screwed y = −0.42 − 0.00841x 0.279
a

For the linear equation, “x” represents the number of months.

b

Comparison of the slope of the equation (variation of MBL in mm in time) between groups.

c

For the cases with available information.

d

It includes 48 implants in 9 former smokers.

FIGURE 1.

FIGURE 1

Scatter plot comparing the marginal bone level over time between implants placed in bruxers and non‐bruxer patients (linear regression).

FIGURE 2.

FIGURE 2

Scatter plot of the marginal bone level measurements in function of time of follow‐up, for non‐bruxer patients.

FIGURE 3.

FIGURE 3

Scatter plot of the marginal bone level measurements in function of time of follow‐up, for probable bruxer patients.

Most categories had a weak degree of linear correlation (R 2 linear) with MBL over time (Table 2). Some categories presented a moderate degree of linear correlation, namely, bruxers, women, implants in mandibles, implants in the molar region, implants with diameter 4.30–5.00 mm, implants supporting prostheses with 7–10 units, and implants with cemented prosthesis. One category presented a strong degree of linear correlation, namely, implants supporting an overdenture.

An additional analysis was performed, investigating the possible synergistic effect of smoking and bruxism on MBL over time (Figure 4). It was observed that a greater MBL is observed when individuals are both bruxers and smokers (y = −0.65 − 0.01000x; R 2 linear = 0.459) when compared to individuals who are either bruxer or smoker (y = −0.49 − 0.00772x; R 2 linear = 0.280), or neither of them (y = −0.31 − 0.00545x; R 2 linear = 0.126), being statistically significant different (p < 0.001).

FIGURE 4.

FIGURE 4

Scatter plot comparing the marginal bone level over time between groups of smokers, bruxers, neither, or both (linear regression).

The results of the linear mixed‐effects model (Table 3) suggested that bruxism, smoking, age, region of the jaws, implant diameter, and prosthesis type had a statistically significant influence on MBL over time.

TABLE 3.

Linear mixed‐effects model for MBL over time.

Predictor variables F statistic p value
Bruxism 469.117 <0.001
Smoking 58.896 <0.001
Age 6.743 0.009
Sex 2.884 0.090
Jaw 3.313 0.076
Region 62.439 <0.001
Implant surface 3.753 0.054
Implant diameter 4.195 0.041
Prosthesis type 13.043 <0.001
Prosthesis fixation 0.250 0.617

4. DISCUSSION

The aim of this study was to investigate whether bruxism leads to greater MBL around dental implants in comparison to non‐bruxers. According to the present results, bruxers presented a statistically significant greater MBL over time than non‐bruxers, especially so when also being a smoker. Therefore, the null hypothesis was rejected.

These results add evidence to the theory stating that bruxism could be a risk factor for MBL surrounding dental implants. 32 The reasoning behind this theory is twofold: (1) Studies have found that bruxers have an increased bite force, 33 which in combination with the lack of periodontal receptors controlling force application surrounding implants 34 might lead to a greater risk of overloading; and (2) The grinding movements associated with bruxing episodes are more likely to expose implants to unfavorable non‐axial forces leading to high‐stress values on the surrounding bone. 32 A finite element analysis study on the effect of different loading conditions on implants showed that the resulting strain intensity in the bone is highest around the cervical neck of the implant. The same study also showed that the stress on the cervical bone increases with more horizontal forces. 35 The overloading combined with high values of eccentric stress is thought to cause microfractures in the surrounding bone crest and disturb the natural balance between bone‐remodeling and resorption, leading to greater MBL in bruxers when compared to non‐bruxers. 36 , 37 As far as the authors of the present study are aware, this is the first human clinical study to compare MBL around implants between balanced groups of bruxer and non‐bruxer patients. Therefore, there are no previous studies to which the present MBL results can be compared to, at least when it comes to bruxism.

Smoking was also suggested to have a significant effect on MBL over time. This is in agreement with the results of previous reviews on the subject, which have found smoking to be a risk factor for both implant failure and increased MBL around implants. 38 , 39 Thus, higher MBL around implants in smokers in comparison to non‐smokers has been observed in a series of clinical studies. 38 Exposure to nicotine is believed to be the mechanism behind this correlation, as it causes vasoconstriction, reducing blood flow and the supply of nutrients necessary for bone formation and remodeling. 40 Moreover, nicotine has been shown to suppress gene expression of certain enzymes involved in the regulation of osteoblast differentiation, proliferation, and apoptosis, which directly affects the bone remodeling process. 41

A synergetic effect of bruxism and smoking was suggested by the present study. Patients who were both bruxers and smokers showed significantly more MBL over time in comparison to patients who were either a smoker or bruxer. This effect is maybe not so surprising when taking into consideration that both smoking and bruxism have a negative effect on MBL. The effects of smoking, that is, the reduced supply of nutrients 40 together with the detrimental effects on osteoblasts, 41 most likely hinder the body's ability to adapt to the overload caused by bruxism, hypothetically leading to greater MBL.

The region of implant installation was found to be a significant factor regarding MBL, with implants in the molar and incisor regions showing greater bone loss. This might be due to the fact that implants placed posteriorly in the jaws are more exposed to unfavorable forces during both chewing and bruxism. The occlusal loads are three times higher in the posterior regions compared to anterior regions. 42 Anteriorly, the cause could be of a traumatic type, as the anterior maxilla is an area that is frequently exposed to trauma. 43 , 44 Another reason may be the eccentric stress caused by the axis of loading on implants in the anterior maxillary region. 43 Higher values of MBL in the anterior maxilla in relation to the other regions have been observed in a clinical study. 45 However, some studies have observed no difference in MBL between anterior and posterior regions of the jaws. 46 , 47

MBL around implants also varied depending on the type of prosthesis the implants were supporting. Overdentures represented more bone loss over time compared to other prosthetic constructions such as crowns or FDP. However, as only seven patients with overdentures were included in this study, the small sample size may lead to a high margin of error. The study also included twice as many bruxers with overdentures as non‐bruxers, which naturally leads to a non‐representative result.

There was a significant relationship between age and MBL over time, with increased bone loss in older patients. This corresponds with the knowledge that bone turnover naturally decreases with age, which may lead to an increased loss of bone mass surrounding both teeth and implants. 48 , 49 Low local bone density in the jaws has been associated with advanced age (>50 years). 50 A positive correlation between patient age and MBL was also observed in other clinical studies, 45 , 51 although there are contrasting results in the literature. 47

Other factors that showed a correlation with increased MBL were implant diameter, region of implant, and type of prosthesis, but the categories of these variables were very unbalanced in frequency, making it impossible to draw robust conclusions from these factors.

Although the patients suspected to be bruxers were called back for clinical examination in order to be able to classify them as probable bruxers, most of the study had a retrospective nature, meaning that all the used data were extracted from patient records. Retrospective studies, while cost‐ and time‐efficient, have several limitations due to their design. Because they are based on review of patient records that were not specifically written with the purpose of collecting data for research, there is always a risk that potentially important information was not recorded, 52 such as the fabrication and frequency of use of night guards by the patients. The present results may however be applied to the general population, as there were no restrictions concerning the inclusion of patients other than the radiological follow‐up.

There is a need for further research into this topic in order to add more evidence to the suggestion that bruxism can be considered a risk factor for implant treatment, although not a contraindication. 16

In conclusion, the present results suggest a significant correlation between bruxism and increased MBL over time around dental implants. In addition, it is suggested that older age, smoking, as well as the combination of bruxism and smoking further increase the risk of MBL over time.

AUTHOR CONTRIBUTIONS

Camila Vu: Investigation, Writing‐original draft, Writing‐review & editing.

Clara Bredberg: Investigation, Writing‐original draft, Writing‐review & editing.

Birgitta Häggman‐Henrikson: Conceptualization, Writing‐review & editing, Visualization, Supervision.

Bruno R. Chrcanovic: Conceptualization, Methodology, Investigation, Data curation, Formal analysis, Writing‐original draft, Writing‐review & editing, Visualization, Supervision.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

ACKNOWLEDGMENTS

This work was supported by Folktandvården Skåne AB, Sweden.

The study was approved by the regional Ethical Committee, Lund, Sweden (Dnr 2014/598; Dnr 2015/72).

Trial registration at the U.S. National Institutes of Health (clinicaltrials.gov): NCT02369562.

Bredberg C, Vu C, Häggman‐Henrikson B, Chrcanovic BR. 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(1):124‐132. doi: 10.1111/cid.13161

Clara Bredberg and Camila Vu contributed equally to this work.

Funding information Folktandvården Skåne AB

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

REFERENCES

  • 1. Manfredini D, Winocur E, Guarda‐Nardini L, Paesani D, Lobbezoo F. Epidemiology of bruxism in adults: a systematic review of the literature. J Orofac Pain. 2013;27(2):99‐110. [DOI] [PubMed] [Google Scholar]
  • 2. Xhonga FA. Bruxism and its effect on the teeth. J Oral Rehabil. 1977;4(1):65‐76. [DOI] [PubMed] [Google Scholar]
  • 3. Johansson A, Omar R, Carlsson GE. Bruxism and prosthetic treatment: a critical review. J Prosthodont Res. 2011;55(3):127‐136. [DOI] [PubMed] [Google Scholar]
  • 4. Kinsel RP, Lin D. Retrospective analysis of porcelain failures of metal ceramic crowns and fixed partial dentures supported by 729 implants in 152 patients: patient‐specific and implant‐specific predictors of ceramic failure. J Prosthet Dent. 2009;101(6):388‐394. [DOI] [PubMed] [Google Scholar]
  • 5. Jiménez‐Silva A, Peña‐Durán C, Tobar‐Reyes J, Frugone‐Zambra R. Sleep and awake bruxism in adults and its relationship with temporomandibular disorders: a systematic review from 2003 to 2014. Acta Odontol Scand. 2017;75(1):36‐58. [DOI] [PubMed] [Google Scholar]
  • 6. Marklund S, Häggman‐Henrikson B, Wänman A. Risk factors associated with incidence and persistence of frequent headaches. Acta Odontol Scand. 2014;72(8):788‐794. [DOI] [PubMed] [Google Scholar]
  • 7. Vieira KRM, Folchini CM, Heyde M, Stuginski‐Barbosa J, Kowacs PA, Piovesan EJ. Wake‐up headache is associated with sleep bruxism. Headache. 2020;60(5):974‐980. [DOI] [PubMed] [Google Scholar]
  • 8. Boscato N, Nascimento GG, Leite FRM, Horta BL, Svensson P, Demarco FF. Role of occlusal factors on probable bruxism and orofacial pain: data from the 1982 Pelotas birth cohort study. J Dent. 2021;113:103788. [DOI] [PubMed] [Google Scholar]
  • 9. Brägger U, Aeschlimann S, Burgin W, Hämmerle CH, Lang NP. Biological and technical complications and failures with fixed partial dentures (FPD) on implants and teeth after four to five years of function. Clin Oral Implants Res. 2001;12(1):26‐34. [DOI] [PubMed] [Google Scholar]
  • 10. De Boever AL, Keersmaekers K, Vanmaele G, Kerschbaum T, Theuniers G, De Boever JA. Prosthetic complications in fixed endosseous implant‐borne reconstructions after an observations period of at least 40 months. J Oral Rehabil. 2006;33(11):833‐839. [DOI] [PubMed] [Google Scholar]
  • 11. Maló P, Nobre M, Lopes A. The rehabilitation of completely edentulous maxillae with different degrees of resorption with four or more immediately loaded implants: a 5‐year retrospective study and a new classification. Eur J Oral Implantol. 2011;4(3):227‐243. [PubMed] [Google Scholar]
  • 12. Chrcanovic BR, 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(7):e1‐e9. [DOI] [PubMed] [Google Scholar]
  • 13. Chrcanovic BR, Kisch J, Larsson C. Retrospective clinical evaluation of 2‐ to 6‐unit implant‐supported fixed partial dentures: mean follow‐up of 9 years. Clin Implant Dent Relat Res. 2020;22(2):201‐212. [DOI] [PubMed] [Google Scholar]
  • 14. Chrcanovic BR, Kisch J, Larsson C. Analysis of technical complications and risk factors for failure of combined tooth‐implant‐supported fixed dental prostheses. Clin Implant Dent Relat Res. 2020;22(4):523‐532. [DOI] [PubMed] [Google Scholar]
  • 15. Chrcanovic BR, Kisch J, Larsson C. Retrospective evaluation of implant‐supported full‐arch fixed dental prostheses after a mean follow‐up of 10 years. Clin Oral Implants Res. 2020;31(7):634‐645. [DOI] [PubMed] [Google Scholar]
  • 16. Chrcanovic BR, Kisch J, Albrektsson T, Wennerberg A. Bruxism and dental implant failures: a multilevel mixed effects parametric survival analysis approach. J Oral Rehabil. 2016;43(11):813‐823. [DOI] [PubMed] [Google Scholar]
  • 17. Chrcanovic BR, Kisch J, Albrektsson T, Wennerberg A. A retrospective study on clinical and radiological outcomes of oral implants in patients followed up for a minimum of 20 years. Clin Implant Dent Relat Res. 2018;20(2):199‐207. [DOI] [PubMed] [Google Scholar]
  • 18. Chrcanovic BR, Kisch J, Albrektsson T, Wennerberg A. Factors influencing the fracture of dental implants. Clin Implant Dent Relat Res. 2018;20(1):58‐67. [DOI] [PubMed] [Google Scholar]
  • 19. Isidor F. Influence of forces on peri‐implant bone. Clin Oral Implants Res. 2006;17(Suppl 2):8‐18. [DOI] [PubMed] [Google Scholar]
  • 20. Pellegrini G, Canullo L, Dellavia C. Histological features of peri‐implant bone subjected to overload. Ann Anat. 2016;206:57‐63. [DOI] [PubMed] [Google Scholar]
  • 21. Quirynen M, Naert I, van Steenberghe D. Fixture design and overload influence marginal bone loss and fixture success in the Branemark system. Clin Oral Implants Res. 1992;3(3):104‐111. [DOI] [PubMed] [Google Scholar]
  • 22. Heitz‐Mayfield LJ, Schmid B, Weigel C, et al. Does excessive occlusal load affect osseointegration? An experimental study in the dog. Clin Oral Implants Res. 2004;15(3):259‐268. [DOI] [PubMed] [Google Scholar]
  • 23. Lima LA, Bosshardt DD, Chambrone L, Araujo MG, Lang NP. Excessive occlusal load on chemically modified and moderately rough titanium implants restored with cantilever reconstructions. An experimental study in dogs. Clin Oral Implants Res. 2019;30(11):1142‐1154. [DOI] [PubMed] [Google Scholar]
  • 24. Miyata T, Kobayashi Y, Araki H, Ohto T, Shin K. The influence of controlled occlusal overload on peri‐implant tissue. Part 3: a histologic study in monkeys. Int J Oral Maxillofac Implants. 2000;15(3):425‐431. [PubMed] [Google Scholar]
  • 25. Duyck J, Rønold HJ, Van Oosterwyck H, Naert I, Vander Sloten J, Ellingsen JE. The influence of static and dynamic loading on marginal bone reactions around osseointegrated implants: an animal experimental study. Clin Oral Implants Res. 2001;12(3):207‐218. [DOI] [PubMed] [Google Scholar]
  • 26. Ferrari DS, Piattelli A, Iezzi G, Faveri M, Rodrigues JA, Shibli JA. Effect of lateral static load on immediately restored implants: histologic and radiographic evaluation in dogs. Clin Oral Implants Res. 2015;26(4):e51‐e56. [DOI] [PubMed] [Google Scholar]
  • 27. Lobbezoo F, Ahlberg J, Raphael KG, et al. International consensus on the assessment of bruxism: report of a work in progress. J Oral Rehabil. 2018;45(11):837‐844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. AASM . International Classification of Sleep Disorders, Revised: Diagnostic and Coding Manual. American Academy of Sleep Medicine Chicago. 2014. [Google Scholar]
  • 29. Paesani DA, Lobbezoo F, Gelos C, Guarda‐Nardini L, Ahlberg J, Manfredini D. Correlation between self‐reported and clinically based diagnoses of bruxism in temporomandibular disorders patients. J Oral Rehabil. 2013;40(11):803‐809. [DOI] [PubMed] [Google Scholar]
  • 30. Treede RD, Jensen TS, Campbell JN, et al. Neuropathic pain: redefinition and a grading system for clinical and research purposes. Neurology. 2008;70(18):1630‐1635. [DOI] [PubMed] [Google Scholar]
  • 31. D'Agostino RB Jr. Propensity score methods for bias reduction in the comparison of a treatment to a non‐randomized control group. Stat Med. 1998;17(19):2265‐2281. [DOI] [PubMed] [Google Scholar]
  • 32. Lobbezoo F, Brouwers JE, Cune MS, Naeije M. Dental implants in patients with bruxing habits. J Oral Rehabil. 2006;33(2):152‐159. [DOI] [PubMed] [Google Scholar]
  • 33. Dıraçoğlu D, Alptekin K, Cifter ED, Güçlü B, Karan A, Aksoy C. Relationship between maximal bite force and tooth wear in bruxist and non‐bruxist individuals. Arch Oral Biol. 2011;56(12):1569‐1575. [DOI] [PubMed] [Google Scholar]
  • 34. Svensson KG, Trulsson M. Impaired force control during food holding and biting in subjects with tooth‐ or implant‐supported fixed prostheses. J Clin Periodontol. 2011;38(12):1137‐1146. [DOI] [PubMed] [Google Scholar]
  • 35. Marcián P, Wolff J, Horáčková L, Kaiser J, Zikmund T, Borák L. Micro finite element analysis of dental implants under different loading conditions. Comput Biol Med. 2018;96:157‐165. [DOI] [PubMed] [Google Scholar]
  • 36. Chrcanovic BR, Albrektsson T, Wennerberg A. Bruxism and dental implants: a meta‐analysis. Implant Dent. 2015;24(5):505‐516. [DOI] [PubMed] [Google Scholar]
  • 37. Zhou Y, Gao J, Luo L, Wang Y. Does bruxism contribute to dental implant failure? A systematic review and meta‐analysis. Clin Implant Dent Relat Res. 2016;18(2):410‐420. [DOI] [PubMed] [Google Scholar]
  • 38. Chrcanovic BR, Albrektsson T, Wennerberg A. Smoking and dental implants: a systematic review and meta‐analysis. J Dent. 2015;43(5):487‐498. [DOI] [PubMed] [Google Scholar]
  • 39. Mustapha AD, Salame Z, Chrcanovic BR. Smoking and dental implants: a systematic review and meta‐analysis. Medicina (Kaunas). 2021;58(1):39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Wang Y, Wan C, Deng L, et al. The hypoxia‐inducible factor alpha pathway couples angiogenesis to osteogenesis during skeletal development. J Clin Invest. 2007;117(6):1616‐1626. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. Deng ZL, Sharff KA, Tang N, et al. Regulation of osteogenic differentiation during skeletal development. Front Biosci. 2008;13:2001‐2021. [DOI] [PubMed] [Google Scholar]
  • 42. Castellanos‐Cosano L, Rodriguez‐Perez A, Spinato S, et al. Descriptive retrospective study analyzing relevant factors related to dental implant failure. Med Oral Patol Oral Cir Bucal. 2019;24(6):e726‐e738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Geckili O, Bilhan H, Geckili E, Cilingir A, Mumcu E, Bural C. Evaluation of possible prognostic factors for the success, survival, and failure of dental implants. Implant Dent. 2014;23(1):44‐50. [DOI] [PubMed] [Google Scholar]
  • 44. Tolstunov L. Implant zones of the jaws: implant location and related success rate. J Oral Implantol. 2007;33(4):211‐220. [DOI] [PubMed] [Google Scholar]
  • 45. Castellanos‐Cosano L, Carrasco‐Garcia A, Corcuera‐Flores JR, Silvestre‐Rangil J, Torres‐Lagares D, Machuca‐Portillo G. An evaluation of peri‐implant marginal bone loss according to implant type, surgical technique and prosthetic rehabilitation: a retrospective multicentre and cross‐sectional cohort study. Odontology. 2021;109(3):649‐660. [DOI] [PubMed] [Google Scholar]
  • 46. Koller CD, Pereira‐Cenci T, Boscato N. Parameters associated with marginal bone loss around implant after prosthetic loading. Braz Dent J. 2016;27(3):292‐297. [DOI] [PubMed] [Google Scholar]
  • 47. Di Domênico MB, Farias Collares K, Bergoli CD, dos Santos MBF, Corazza PH, Özcan M. Factors related to early marginal bone loss in dental implants—a multicentre observational clinical study. Appl Sci. 2021;11(23):11197. [Google Scholar]
  • 48. Huttner EA, Machado DC, de Oliveira RB, Antunes AG, Hebling E. Effects of human aging on periodontal tissues. Spec Care Dentist. 2009;29(4):149‐155. [DOI] [PubMed] [Google Scholar]
  • 49. Shirota T, Ohno K, Suzuki K, Michi K. The effect of aging on the healing of hydroxylapatite implants. J Oral Maxillofac Surg. 1993;51(1):51‐56. [PubMed] [Google Scholar]
  • 50. He J, Zhao B, Deng C, Shang D, Zhang C. Assessment of implant cumulative survival rates in sites with different bone density and related prognostic factors: an 8‐year retrospective study of 2,684 implants. Int J Oral Maxillofac Implants. 2015;30(2):360‐371. [DOI] [PubMed] [Google Scholar]
  • 51. Negri M, Galli C, Smerieri A, et al. 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. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Talari K, Goyal M. Retrospective studies ‐ utility and caveats. J R Coll Physicians Edinb. 2020;50(4):398‐402. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.


Articles from Clinical Implant Dentistry and Related Research are provided here courtesy of Wiley

RESOURCES