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(Stroke. 2004;35:2029.)
© 2004 American Heart Association, Inc.
Original Contributions |
From the Division of Epidemiology (M.D., R.T.D., D.R.J.), School of Public Health, and the Division of Infectious Disease and International Medicine, Department of Medicine, Medical School, University of Minnesota; the International Training and Research Program in Infectious Disease Epidemiology (INTREPIDE) Initiative in Global Heath (M.D.); the Abteilung Parodontologie (C.S., T.K.), Zentrum Zahn-, Mund und Kieferheilkunde, Institut für Epidemiologie und Sozialmedizin (H.V., U.J.), the Institut für Klinische Chemie (J.L.), and the Klinik für Neurologie (C.K.), University of Greifswald, Germany; and the Institute for Nutrition Research (D.R.J.), University of Oslo, Norway.
Correspondence to Dr Thomas Kocher, Unit of Periodontology, Dental School, Rotgerberstr. 8, 17487 Greifswald, Germany. E-mail kocher{at}uni-greifswald.de
| Abstract |
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Methods A total of 1710 randomly enrolled participants between the ages of 45 and 75 with no history of myocardial infarction or stroke received a clinical periodontal examination, carotid scan using high-resolution B-mode ultrasound, and extensive measurements for conventional cardiovascular risk factors (age, education, smoking, alcohol, body mass index, diabetes, systolic blood pressure, low-density lipoprotein-cholesterol, high-density lipoprotein-cholesterol, and triglycerides) as well as markers of healthy lifestyle and social network.
Results In both genders, measures of current and long-term periodontitis worsened as tooth loss increased. In males but not females, an
10% difference in carotid artery plaque prevalence was observed between the lowest and highest tertiles of tooth loss (P<0.05) and long-term periodontitis (P=0.05) after multivariate adjustment. Similar patterns were observed for intimamedia thickness. The influence of gender on carotid artery plaque prevalence was most evident among the younger age group (<59 years). Between genders, carotid plaque prevalence differed by 10%, 15%, and 25% across increasing levels of tooth loss, and by 5%, 15%, and 25% across increasing levels of long-term periodontitis.
Conclusions Our data suggest that tooth loss and long-term periodontitis are related to subclinical atherosclerosis in men but not women. Gender variations in cardiovascular morbidity or mortality may be explained partly by the differential contributions of novel risk factors across genders.
Key Words: atherosclerosis gender infection periodontal disease tooth loss
| Introduction |
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The relationship between oral health, specifically periodontal disease, and CVD has been a subject of mounting research recently2 and is biologically plausible and supported by data on transient bacteremia and elevated inflammatory markers.3 Because males tend to carry a disproportionate burden of periodontal infections,4 we investigated the modifying role of gender in the relationship between periodontal infections, tooth loss, and subclinical atherosclerosis. We studied whether: (1) a relationship of periodontal infections, tooth loss, and subclinical atherosclerosis exists in the European population of Eastern Germany; (2) this relationship differs by gender; and (3) the differences in CVD rates across gender are explained partly by varying distributions in periodontal infections.
| Materials and Methods |
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For this article, we selected subjects aged 45 to 75 years with no history of myocardial infarction or stroke (n=2124). Among them, 1983 had carotid artery ultrasound performed to measure carotid artery plaque and intimamedia thickness (IMT). Subjects were removed because of missing tooth count (n=4), missing periodontal measurements resulting from crowns (n=128), or absence of teeth in the quadrants measured (n=12). Ninety had incomplete lipids (n=62) or risk factor data (n=28), and 9 refused. Thus, 1740 subjects remained for analyses. Data collection occurred between October 1997 and May 2001 after written consent. The study was approved by the institutional review board of the University of Greifswald.
Dental History and Oral Examination
The oral health examination included an examination of the oral cavity to assess tooth count and location. Flossing and brushing were reported. The periodontal probe PCP 11 (Hufriedy) was used to assess probing depth (PD), gingival recession, and clinical attachment loss (AL) for all examined teeth. Measurements were taken at 4 sites per tooth (mesiobuccal, midbuccal, distobuccal, and midlingual). All periodontal findings were registered according to the half-mouth method on the right or left side in alternate subjects. In this article, we categorized dentate subjects according to the extent of current (as measured by PD) and long-term (as measured by AL) periodontal disease. Disease was defined at a particular level of severity at each site, namely
5 mm for PD and
4 mm for AL. Disease extent was defined by the percentage of periodontal sites meeting the above severity criteria for PD and AL. The percentage of sites was calculated within each mouth by dividing the number of sites with PD
5 mm by the total number of sites measured, and similarly for AL. Tooth loss was categorized as tertiles (0 to 8, 9 to 15, 16 to 31) among the dentate and edentulous.
Calibrated licensed dentists performed the entire examination. Each 6 to 12 months, calibration exercises7 were performed on a subset of persons not connected with the study, yielding an intraclass correlation of 0.82 to 0.91 per examiner and an inter-rater correlation of 0.84 relative to AL.
Ultrasound Examination
Certified examiners scanned the extracranial carotid arteries bilaterally with B-mode ultrasound using a 5-MHz linear probe array transducer and a high-resolution instrument (DIASONICS VST; Gateway Scientific) with the participant in the horizontal position. Plaque occurrence was diagnosed during the examination in the common carotid arteries (CCAs), the bifurcation, and the internal carotid artery (ICA) and external carotid artery (ECA). Plaques were present if a focal widening of the vessel wall relative to adjacent segments was found (as evidenced by protrusion into the lumen or localized roughness with increased echogenicity or an area of focal increased thickness of the intimamedia layer). Plaque presence was defined as
1 plaque in any of the carotid arteries. In addition, scans from the distal straight portion (1 cm in length) of both CCAs were recorded, and the mean far-wall IMT was calculated by averaging the 10 consecutive measurement points (in 1-mm steps) from the bulb of both sites by trained and certified readers.
Risk Factor Assessment
All participants received an extensive medical examination, a computer-guided interview, and a self-administered questionnaire.6 In short, patients were queried by computer-aided face-to-face interviews on sociodemographic characteristics and medical histories regarding hypertension, diabetes, angina pectoris (rose questionnaire), history of myocardial infarction and stroke, as well as rehabilitation history, heart surgery, congestive heart failure, peripheral vascular disease, alcohol use, and current smoking.
Smoking was categorized as never, former, occasional, and current smoker. Continuous assessment was calculated as total pack years of cigarette smoking. The following information was collected: smoking duration (age at smoking cessation minus age at initiation) and the maximum quantity of cigarettes smoked per day during a year. Occasional smoking was defined as <1 cigarette per day. The smoking questionnaire was validated.8
Diabetes was defined as self-reported physician diagnosis of diabetes and pharmacological treatment for diabetes or hemoglobin A1c values
7%. Height and weight were determined using calibrated scales. Blood pressure was measured using a calibrated semiautomatic sphygmomanometer (HEM-705CP; Omron Corp),9 and the average of 3 measurements was used in analysis. Hypertension was defined by self-report of diagnosed hypertension or use of antihypertensive medications, mean systolic blood pressure
140 mm Hg, or mean diastolic blood pressure
90 mm Hg.
Nonfasting blood samples were taken and sent for complete blood count to 2 laboratories. The laboratories participated in the official Germany Institute for Standardization and Documentation in the Medical Laboratory round-robin tests for quality assurance in analytical labs semiannually throughout the data collection period. Moreover, duplicate blood samples were collected and analyzed for internal quality assurance protocol in each examination center once per week. Hemoglobin A1c was measured by cation-exchange chromatography (high-performance liquid chromatography) with spectrophotometric detection (Diamat Analyzer; Bio-Rad). Total cholesterol was measured enzymatically (cholesterol esterase/peroxidase), high-density lipoprotein-cholesterol enzymatically after magnesium chloride precipitation, and low-density lipoprotein-cholesterol after dextranesulfate precipitation.
Assessment of Cultural, Life Style, and Social Network Variables
All participants were white. The self-administered questionnaire included education level and social network. Education was categorized as <9, 9 to 10 years, and
11 years of schooling. Social variables were assessed with 12 questions and covered marital status, number of friends and children, contact with them, and the expressed desire to have more friends or family and the availability of support for personal problems or transportation.
Leisure physical activity was assessed as reporting >2 hours per week, 1 to 2 hours per week, <1 hour per week, and no activity and was then converted into METS, an established measure of metabolic output.10 Alcohol intake during the previous week and weekend was queried for type and frequency of alcohol consumption. The mean daily alcohol consumption for the last week (grams of pure alcohol per day) was calculated by the beverage-specific quantity/frequency method: number of days with alcohol intake (subdivided into 3 beverage types: beer, wine, and spirits).
Statistical Analysis
All analyses were performed in PC-SAS for Windows 8.0. Linear and logistic regression models were used. The number of missing teeth per mouth was modeled continuously and categorically. We estimated the percentage of individuals with any carotid plaque and odds ratios between tooth loss categories using logistic regression. For IMT, adjusted means were compared. We defined age continuously and categorically by 10-year intervals in preliminary analyses. The 2 definitions produced similar results, and all models presented are adjusted for age as a categorical variable. Physical activity, diastolic blood pressure, and social variables in this highly homogeneous population did not meet the criteria for confounding (namely, that inclusion in the model led to
10% change in the coefficient of interest) and were thus excluded from final analyses.
| Results |
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Eighty-four percent of the participants (n=1463) were dentate and had an average of 19.0±7.0 teeth. After age adjustment, dentate males tended to have more teeth (19.2±7.0) than females (18.7±7.0; P=0.12).
The percentage of periodontal sites with PD
5 mm was 10% in males versus 6% in females (P<0.0001). For AL
4 mm, these values were 49% and 37% (P<0.0001), respectively. Additional characteristics of the population are in Table 1.
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Relationship Between Tooth Loss and Clinical Measures of Periodontal Disease
The greater the number of teeth lost, the higher the extent of severe periodontal disease. Across increasing levels of tooth loss, there was a consistent increase in the age-adjusted proportion of sites with severe AL (from 24% to 64%) and PD (from 9% to 25%), the increase being statistically stronger in males (Table 2).
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Conventional Measures of Periodontal Disease, Tooth Loss, and Carotid Atherosclerosis
Atherosclerosis was related to AL and tooth loss in males but not females (Tables 3 and 4
). Plaque was 10% more prevalent among males in the highest tertile of AL compared with those in the lowest tertile (P=0.05). Also, among males with 0 to 8 missing teeth, 66% had carotid artery plaque, whereas among those with
16 missing teeth, prevalence of carotid artery plaque was
75% (P<0.05). Similar patterns were observed for IMT, with males showing adjusted means of 0.80±0.01, 0.80±0.01, 0.81±0.009, and 0.84±0.01 mm (P=0.04 for linear trend) across increasing levels of tooth loss and adjusted means of 0.80±0.01, 0.79±0.009, and 0.82±0.009 mm across tertiles of percentage AL
4 mm (linear trend P=0.11; Figure 1). This gender difference was even stronger with a cut-off of AL
5 mm: in males, IMT thickness increased from 0.79±0.1 to 0.80±0.009 and 0.82±0.009 mm across increasing tertiles of AL (P=0.05 highest/lowest tertile) as opposed to women (0.74±0.009, 0.74±0.009, and 0.73±0.009 mm). Adjustment for brushing and flossing did not alter these conclusions.
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Among the entire population, the relationship was effectively unchanged whether the smoking adjusting variable was smoking status (never, ex-smoker, current smoker) alone or smoking status and pack years (data not shown). Findings were qualitatively similar in nonsmokers.
We further divided the population at median age 59 years. The modifying effect of gender on the relationship between tooth loss and carotid plaque prevalence seemed driven by the younger age groups (<59 years; Figure 2). In the older half of the population, the gender interaction disappeared; the relationship weakened in men, heading for saturation (nearly everyone had plaque), and strengthened in women, from inverse to positive, neither gradient strong. A similar pattern was observed for the relationship between carotid plaque prevalence and AL (Figure 2). The effect of age on IMT was less clear (data not shown).
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| Discussion |
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A recent publication in this journal reported on gender differences in the relationship of periodontal disease with clinical end points.12 Therefore, our data support this report at a subclinical level.
The fact that women had substantially less-documented periodontal disease but had lost an equal number of teeth raises a number of possibilities: they might have lost their teeth for reasons independent of periodontal disease; for reasons related to periodontal diseases but accelerated by other conditions; or tooth removal may be pursued more aggressively in women. A number of studies have reported on the relationship between osteoporosis, periodontal disease, and tooth loss.13,14 It is possible that women might be more likely to experience tooth loss because of their osteoporosis compared with men with similar levels of periodontal disease. In such instances, tooth loss might not be as reliable a marker of past periodontal disease in these postmenopausal women. Further, Splieth et al have shown that dentists in this population extract teeth at an early stage of disease,15 a practice that may differ by gender.
The gender differences reported here might be attributable to treatment bias, practice differences, or sociocultural determinants. Smoking patterns, for example, were different across genders. Although we were careful to adjust for smoking, confounding by smoking cannot be unequivocally excluded. However, the fact that our findings were similar in the subgroup of never smokers makes this possibility less likely.
Other explanations (interaction with obesity and interleukin-6) are possible. Also, because males in this study had
50% more periodontal disease compared with females, it is possible that females did not reach a threshold of inflammation that might have otherwise been associated with severe periodontal infections and carried over to subclinical atherosclerosis until a later age. Also, because younger females seem to have no increased carotid plaque associated with periodontal disease but catch up with men as they age, the possibility of a protective hormonal role cannot be excluded.
Whether the gender differential observed in this study is caused by early tooth extraction, early tooth loss, or true mechanistic differences between the genders as it relates to atherosclerosis cannot be determined cross-sectionally. However, the fact that gender differences were noted for IMT and plaque lends credence to the possibly intrinsic role of gender.
This study shares with others the limitations inherent to cross-sectional data. First, because of a lack of time sequence, the relationships reported here should not be interpreted as causal. Second, only half-mouth examinations were performed, and we had no information on previous periodontal treatment. However, half-mouth examinations16 and previous undocumented treatment are thought to underestimate the extent of periodontal disease, thus likely moving our estimates toward the null. Nevertheless, because all teeth were counted, tooth loss findings are not affected by this limitation. Finally, absent the collection of antibodies to periodontal pathogens or high-sensitivity C-reactive protein, we were limited in our mechanistic exploration of the inflammatory aspect of this relationship.
Previous findings from the multiethnic Oral Infections and Vascular Disease Epidemiology Study (INVEST)11 imply that tooth loss is a marker of past periodontal disease in certain populations. Our results in the vastly different SHIP population seem to support the robustness of this hypothesis. The high atherosclerosis values among the male edentulous (with historically worse periodontal disease) compared with the lower values among female edentulous (historically periodontally healthier) also raise the possibility that the damage may be more preventable rather than reversible once a threshold is reached.
As new factors emerge for CVD, questions should be asked not only regarding their contribution to CVD risk but also, we submit, regarding their potential differential contribution to the gender gap in CVD. In this population, the gender differences in atherosclerosis prevalence seemed to be related not only to the distribution but to the differing contributions of periodontal infections to atherosclerosis across genders.
| Acknowledgments |
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Received February 12, 2004; revision received April 16, 2004; accepted June 1, 2004.
| References |
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