Association between harmful alcohol use and periodontal status according to gender and smoking
- Hyang-Sun Kim†1,
- Ji-Hyun Son†2,
- Hee-Yong Yi3,
- Hae-Kyoung Hong4,
- Hyun-Jun Suh5 and
- Kwang-Hak Bae3, 6Email author
© Kim et al.; licensee BioMed Central Ltd. 2014
Received: 16 April 2014
Accepted: 17 June 2014
Published: 20 June 2014
the aim of this study is to assess the association of harmful alcohol use based on the alcohol use disorders identification test (AUDIT) score with periodontal status according to gender and smoking in a representative sample of Korean adults.
This study analyzed 5,291 participants older than 19 years whose data of harmful alcohol use and periodontal status were available. Harmful alcohol use was defined by the WHO guidelines for the administration of AUDIT. The periodontal status was assessed by the Community Periodontal Index (CPI). Multivariate logistic regression analysis was performed with adjustment for socio-demographic variables, oral and general health behavior, oral health status and systemic conditions. All analyses considered a complex sampling design, and multivariate analysis was also performed in the subgroups.
Multivariate logistic regression analysis revealed a marginal association between harmful alcohol use and higher CPI in the total sample. The adjusted odds ratio (OR) of harmful alcohol use was 1.16 (0.97 to 1.38) for higher CPI. Higher CPI was significantly associated with harmful alcohol use in men (OR: 1.28; 95% CI: 1.03-1.60) and non-smokers (OR: 1.29; 95% CI: 1.06-1.57).
Periodontal status is significantly associated with harmful alcohol use in men and non-smokers in a representative sample of Korean adults.
KeywordsHarmful Alcohol use Periodontal status Association Gender Smoking
Periodontitis is a chronic and long-lasting low-grade inflammatory disease that leads to a break-down of the connective tissue and bone that anchors the teeth to the jaws [1, 2]. It is a highly prevalent disease worldwide contributing to the global burden of chronic diseases and represents a major public health problem in many countries [3, 4]. In Korea, the prevalence of periodontitis is 29.4% among adults . Periodontitis is also related to systemic alterations such as atherosclerotic vascular disease and metabolic syndrome [6, 7].
Long-term and excessive alcohol consumption can influence host defenses causing toxic damage, which is implicated in a wide variety of diseases, disorders, and injuries such as oro-pharyngeal cancer, liver cirrhosis, pancreatitis, hypertension, gastritis, diabetes, some forms of stroke, and mental disorders such as depression [8–10].
As chronic and even acute, moderate alcohol use can increase host susceptibility to infections caused by bacterial pathogens and impaired host defense after alcohol exposure appears to be linked to a combination of decreased inflammatory response, altered cytokine production, and abnormal reactive oxygen intermediate generation , it may be related to periodontitis independently of other potential confounders.
However, a recent systematic review reported that, among 14 studies, only 3 studies showed clear association, and 6 studies showed marginal or weak association of alcohol consumption or dependence with periodontitis, while the other 5 studies did not find significant association . Moreover, there was much diversity in the way of measuring alcohol consumption, and most studies considered limited potential confounders or examined non-representative small samples [10, 12, 13]. Hence, further studies are needed to elucidate whether or not alcohol consumption is a risk factor for periodontitis.
The Alcohol use disorders identification test (AUDIT) was developed by the World Health Organization (WHO) and validated by lots of studies as a simple method of screening for excessive drinking as the cause of the presenting illness, which is the only screening test specifically designed for international use, and in comparison to other screening tests, the AUDIT has been found to perform equally well or at a higher degree of accuracy across a wide variety of criterion measures .
When investigating the periodontitis-associated factors, effect modification needs to be considered in an appropriate manner in epidemiological studies because multivariate models with a single estimate require homogeneity of the effect across different levels of extraneous variables such as gender and smoking .
However, there are few studies on the association between alcohol consumption based on AUDIT score and periodontitis in a nationally representative sample considering effect modification.
Therefore, the aim of this study is to assess the association of harmful alcohol use based on AUDIT score with periodontal status according to gender and smoking in a representative sample of Korean adults.
Study design and subject selection
The data included a subset of the Fourth Korea National Health and Nutrition Examination Survey (KNHANES) conducted in 2009 by the Korea Center for Disease Control and Prevention (KCDC). The sampling protocol for the KNHANES was designed to involve a complex, stratified, multistage, probability-cluster survey of a representative sample of the non-institutionalized civilian population in Korea. The survey was performed by the Korean Ministry of Health and Welfare. The target population of the survey was all non-institutionalized civilian Korean individuals aged 1 year or older. The survey employed stratified multistage probability sampling units based on geographic area, gender, and age, which were determined based on the household registries of the 2005 National Census Registry, the most recent 5-year national census in Korea. Using the 2005 census data, 200 primary sampling units (PSU) were selected across Korea. The final sample set for KNHANES included 4,600 households. Among 12,722 sampled individuals, the number of participants was 10,533. The response rate was 82.8%. A total of 7,893 individuals aged over 19 participated in KNHANES, but 5,291 of the participants, who received a periodontal examination, were examined for AUDIT. A detailed description of the sampling was described in the KNHANES report .
The WHO community periodontal index (CPI) was used to assess periodontal status. Higher CPI was defined as a CPI greater than or equal to ‘code 3’, which indicates that at least one site had a > 3.5 mm (code 4 > 5.5 mm) – probing pocket depth. The index tooth numbers were 11, 16, 17, 26, 27, 31, 36, 37, 46 and 47.
A CPI probe that met the WHO guidelines was used . The mouth was divided into sextants. An approximately 20 g probing force was used. In 2009 KNHANES, 27 trained dentists examined the periodontal status of the subjects. The inter-examiner mean of kappa value was 0.77 (0.53 to 0.94) .
Harmful alcohol use
The AUDIT was administered as a self-report questionnaire composed of 10 questions including frequency of drinking, typical quantity, frequency of heavy drinking, impaired control over drinking, increased salience of drinking, morning drinking, guilt after drinking, blackouts, alcohol-related injuries, and others concerned about drinking (see Additional file 1: Table S1). Each of the questions has a response with a score ranging from 0 to 4. The participants with a total AUDIT score of 8 or higher were assessed as harmful alcohol use according to the WHO guidelines for the administration of AUDIT .
The socio-demographic variables included gender, age, household income, and educational level. Household income was the family income adjusting for the number of family members. The educational level was assessed by highest diploma.
The oral health behaviors included daily frequency of toothbrushing and use of dental floss or interdental brush. As general health behavior, current smoking status was included. According to the current smoking status, the participants were divided to 3 groups (Non-smokers: those who had never smoked or had smoked fewer than 100 cigarettes in their life, current smokers: those who were currently smoking and had smoked 100 cigarettes or more in their whole life, past smokers: those who had smoked in the past but they stopped smoking at that time).
The oral health status included the number of decayed permanent teeth (DT), which was examined and summarized according to WHO criteria . The systemic conditions included diabetes and obesity.
The individual weighted factors were used and the complex sampling design of the survey was considered to obtain the variances. Multivariate logistic regression analyses were applied to examine the relationships between harmful alcohol use and periodontal status. The odds ratios of harmful alcohol use for higher CPI were adjusted for above-mentioned covariates in logistic model. Because the interaction terms of periodontal status with gender and smoking was significant, subgroup analyses were performed to gain estimates stratified according to gender and smoking. Statistical analyses were performed using SPSS version 19.0 software (SPSS, Chicago, IL, USA).
Bivariate comparisons of the characteristics between the participants with lower and higher CPI
Gender (n = 5291)
Highest diploma (n = 5283)
≥ University or college
Household income† (n = 5247)
25 - 50%
50 - 75%
Diabetes (n = 5291)
Obesity‡ (n = 5251)
Oral health behaviors
Daily frequency of toothbrushing (n = 5291)
Once or less
Three times or more
Use of floss or interdental brush (n = 5291)
General health behaviors
Harmful alcohol use§ (n = 5291)
Present smoking status (n = 5282)
Adjusted odds ratios (OR) and 95% confidence intervals (CI) of harmful alcohol use (AUDIT score ≥ 8) for higher CPI in total sample and each subgroup
In this study, an association was found between harmful alcohol use and periodontal status after adjusting for the socio-demographic variables, oral and general health behaviors, and oral health status, especially in men and non-smokers.
While alcohol consumption has been widely perceived as a risk factor of periodontitis due to the biological plausibility based on the relationship between alcohol use and impaired systemic conditions such as reduced resistance to infection and liver damage [19–21], several studies reported a negative correlation between alcohol consumption and periodontitis based on longitudinal and cross-sectional researches.
For example, Jansson  conducted a longitudinal investigation of 513 individuals from the County of Stockholm in 1970 and 1990. He did not find any significant association between alcohol consumption and periodontitis. Even though the subjects with higher alcohol consumption had calculus more frequently than those with lower alcohol consumption, alcohol consumption was not associated with periodontitis. Torrungruang et al.  performed a cross-sectional survey targeting 2,005 people aged 50 to 73 years in Thailand, and also reported that alcohol consumption had no significant effect on the severity of periodontal disease severity in the multivariate model.
This disparity might be due to differences in the potential confounders, assessment of alcohol consumption, criteria of periodontitis, and ethnical backgrounds. In addition, effect modification could be another reason for the variation. Most previous studies on the association between alcohol consumption and periodontitis did not consider effect modifiers. Ylöstalo et al.  reported that effect modification was not always treated in an appropriate manner in epidemiological studies although it was a basic concept in quantitative research. Based on the analysis of simulation data, they concluded that effect modification might explain the variation in the results of studies on the association between periodontitis and systemic disease. In this study, as we found significant interaction terms, subgroup analysis was performed with subgroups stratified by the levels of effect modifiers. The results of this study did not support the association between harmful alcohol use and periodontal status in the total sample. However, subgroup analysis showed that harmful alcohol use was significantly associated with higher CPI in men and non-smokers.
To the best of our knowledge, this is the first study to report gender and smoking as effect modifying factors of the association between alcohol consumption and periodontal status. Some studies reported that smoking and alcohol consumption are associated with increased risk of systemic diseases such as fatty liver disease and metabolic syndrome, especially when these two exposures occur together [24, 25]. The result of this study is opposite to those previous results. However, considering that smoking is one of the strongest risk factors for periodontitis , it could be inferred that smoking may mask the effect of alcohol consumption on periodontal health in smokers.
Briasoulis et al.  found that the association between light to moderate alcohol intake and the risk of developing hypertension differed between women and men. They explained that differences in the pattern of drinking, beverage choices, and smoking habits may contribute to the observed sex differences because the health effects of drinking may depend on drinking pattern, and failure to differentiate episodic from regular drinkers may obscure the real associations. It is consistent with the gender difference found in this study.
Further studies will be needed to elucidate the association between alcohol consumption and periodontal status according to gender and smoking.
The difference in the assessment of alcohol consumption is also suggested to be one of the explanations for the variation in the results of the studies on the association between alcohol consumption and periodontal status. Amaral Cda et al.  reported that alcohol consumption was assessed by various unvalidated questionnaires with different criteria varied according to researchers in lots of studies. Therefore, this study used the AUDIT to determine harmful alcohol use.
The AUDIT was developed by the WHO and validated by lots of studies as a screening tool for excessive drinking . Epidemiologic studies have used the AUDIT [28, 29]. In order to evaluate the AUDIT against other common screening measures, Allen et al.  reviewed the studies in which the sensitivity and specificity of the AUDIT were contrasted with those of the alternative measures. They found that the AUDIT performed at a level at least comparable with and generally exceeding that of the alternate measures. However, there have been few studies on the association between periodontitis and alcohol consumption based on AUDIT .
This study had several limitations. The periodontal status was assessed by CPI. Although CPI is an easier way to assess the prevalence of periodontitis in a population survey and has been adopted as an index for periodontitis in epidemiologic studies on the association between systemic health and periodontal disease , the limitation of CPI should be deliberately considered since it can overestimate or underestimate the prevalence of periodontitis due to the use of representative teeth and pseudo pockets . Therefore, the term of higher CPI was used instead of periodontitis to classify periodontal status. Another important limitation of this study is its cross-sectional design, which makes it impossible to determine the direction of the causal relationship of harmful alcohol use with periodontal status. As the association of subgroups found in this study was so weak, further studies will be needed to confirm the association between harmful alcohol use and periodontal status in men and non-smokers.
Nevertheless, this is the first epidemiologic study to report an effect modification of the association between harmful alcohol use and periodontal status by gender and smoking in a nationally representative sample of adults.
Periodontal status is significantly associated with harmful alcohol use defined using the AUDIT in men and non-smokers. The underlying mechanisms showing an effect modification of the association between harmful alcohol use and periodontal status by gender and smoking remain to be determined through prospective cohort studies.
Human subjects approval statement
The study was conducted in compliance with the principles of the Helsinki Declaration. Ethical clearance of the study was approved by the Institutional Review Board (IRB) of Korea Centers for Disease Control and Prevention (IRB number. 2009-01CON-03-2C).
The study was self-supported, but the Korea Center for Disease Control and Prevention provided the data of the Fourth Korea National Health and Nutrition Examination Survey to be used in the study.
- Li P, He L, Sha YQ, Luan QX: Relationship of metabolic syndrome to chronic periodontitis. J Periodontol. 2009, 80: 541-549. 10.1902/jop.2009.080387.View ArticlePubMedGoogle Scholar
- Williams RC: Periodontal disease. N Engl J Med. 1990, 323: 373-382. 10.1056/NEJM199008093230603.View ArticleGoogle Scholar
- Albander JM, Bunelle JA, Kingman A: Destructive periodontal disease in adults 30 years of age and older in the United States, 1988–1994. J Periodontol. 1999, 70: 13-29. 10.1902/jop.19220.127.116.11.View ArticleGoogle Scholar
- Petersen PE, Ogawa H: The global burden of periodontal disease: towards integration with chronic disease prevention and control. Periodontol 2000. 2012, 60: 15-39. 10.1111/j.1600-0757.2011.00425.x.View ArticlePubMedGoogle Scholar
- Korea Center for Disease Control and Prevention & Ministry of Health and Welfare: Korean National Health and Examination Surveys: the 4th surveys. 2013, https://knhanes.cdc.go.kr/knhanes/index.do. Accessed on 22 November, 2013Google Scholar
- Bullon P, Newman HN, Battino M: Obesity, diabetes mellitus, atherosclerosis and chronic periodontitis: a shared pathology via oxidative stress and mitochondrial dysfunction?. Periodontol 2000. 2014, 64: 139-153. 10.1111/j.1600-0757.2012.00455.x.View ArticlePubMedGoogle Scholar
- Nibali L, Tatarakis N, Needleman I, Nibali L, Tatarakis N, Needleman I, Tu YK, D'Aiuto F, Rizzo M, Donos N: Clinical review: Association between metabolic syndrome and periodontitis: a systematic review and meta-analysis. J Clin Endocrinol Metab. 2013, 98: 913-920. 10.1210/jc.2012-3552.View ArticlePubMedGoogle Scholar
- World Health Organization: Problems related to alcohol consumption, Report of a WHO Expert Committee. 1980, Geneva: Tech. Report Series 650. World Health Organization,Google Scholar
- Edwards G, Anderson P, Babor TF, Edwards G, Anderson P, Babor T, Casswell S, Ferrence R, Giesbrecht N, Godfrey C, Holder Harold D, Lemmens P, Makela K, Midanik Lorraine T, Norstrom T, Osterberg E, Romelsjo A, Room R, Simpura J, Skog O-J: Alcohol Policy and the Public Good. 1994, Oxford: Oxford University PressGoogle Scholar
- Amaral Cda S, Vettore MV, Leão A: The relationship of alcohol dependence and alcohol consumption with periodontitis: a systematic review. J Dent. 2009, 37: 643-651. 10.1016/j.jdent.2009.04.011.View ArticlePubMedGoogle Scholar
- Szabo G: Consequences of alcohol consumption on host defence. Alcohol Alcohol. 1999, 34: 830-841. 10.1093/alcalc/34.6.830.View ArticlePubMedGoogle Scholar
- Shizukuishi S, Hayashi N, Tamagawa H, Shizukuishi S, Hayashi N, Tamagawa H, Hanioka T, Maruyama S, Takeshita T, Morimoto K: Lifestyle and periodontal health status of Japanese factory workers. Ann Periodontol. 1998, 3: 303-311. 10.1902/annals.1918.104.22.1683.View ArticlePubMedGoogle Scholar
- Khocht A, Janal M, Schleifer S, Keller S: The influence of gingival margin recession on loss of clinical attachment in alcohol-dependent patients without medical disorders. J Periodontol. 2003, 74: 485-493. 10.1902/jop.2003.74.4.485.View ArticlePubMedGoogle Scholar
- World Health Organization: The Alcohol Use Disorders Identification Test: Guidelines for Use in Primary Care, 2n edition. 8–20. 2001, Geneva: World Health OrganizationGoogle Scholar
- Ylöstalo PV, Knuuttila ML: Confounding and effect modification: possible explanation for variation in the results on the association between oral and systemic diseases. J Clin Periodontol. 2006, 33: 104-108. 10.1111/j.1600-051X.2005.00886.x.View ArticlePubMedGoogle Scholar
- World Health Organization: Oral Health Surveys: Basic Methods, 4th edition. 6–39. 1997, Geneva: World Health OrganizationGoogle Scholar
- Korea Center for Disease Control and Prevention: Standardization for Oral Health Survey in KNHANES (2009). 2010, Seoul: Korea Center for Disease Control and PreventionGoogle Scholar
- WHO: Oral health survey, basic methods. 1997, Geneva: World Health Organization, 4Google Scholar
- Curtis BJ, Zahs A, Kovacs EJ: Epigenetic targets for reversing immune defects caused by alcohol exposure. Alcohol Res. 2103, 35: 97-113.Google Scholar
- Genco RJ, Borgnakke WS: Risk factors for periodontal disease. Periodontol 2000. 2013, 62: 59-94. 10.1111/j.1600-0757.2012.00457.x.View ArticlePubMedGoogle Scholar
- Persson EC, Schwartz LM, Park Y, Persson EC, Schwartz LM, Park Y, Trabert B, Hollenbeck AR, Graubard BI, Freedman ND, McGlynn KA: Alcohol consumption, folate intake, hepatocellular carcinoma, and liver disease mortality. Cancer Epidemiol Biomarkers Prev. 2013, 22: 415-421. 10.1158/1055-9965.EPI-12-1169.View ArticlePubMedPubMed CentralGoogle Scholar
- Jansson L: Association between alcohol consumption and dental health. J Clin Periodontal. 2008, 35: 379-384. 10.1111/j.1600-051X.2008.01210.x.View ArticleGoogle Scholar
- Torrungruang K, Tamsailom S, Rojanasomsith K, Torrungruang K, Tamsailom S, Rojanasomsith K, Sutdhibhisal S, Nisapakultorn K, Vanichjakvong O, Prapakamol S, Premsirinirund T, Pusiri T, Jaratkulangkoon O, Unkurapinun N, Sritara P: Risk indicators of periodontal disease in older Thai adults. J Periodontol. 2005, 76: 558-565. 10.1902/jop.2005.76.4.558.View ArticlePubMedGoogle Scholar
- Nakashita Y, Nakamura M, Kitamura A, Kiyama M, Ishikawa Y, Mikami H: Relationships of cigarette smoking and alcohol consumption to metabolic syndrome in Japanese men. J Epidemiol. 2010, 20: 391-397. 10.2188/jea.JE20100043.View ArticlePubMedPubMed CentralGoogle Scholar
- Park EY, Lim MK, Oh JK, Park EY, Lim MK, Oh JK, Cho H, Bae MJ, Yun EH, Kim DI, Shin HR: Independent and supra-additive effects of alcohol consumption, cigarette smoking, and metabolic syndrome on the elevation of serum liver enzyme levels. PLoS ONE. 2013, 8: e63439-10.1371/journal.pone.0063439.View ArticlePubMedPubMed CentralGoogle Scholar
- Nunn ME: Understanding the etiology of periodontitis: an overview of periodontal risk factors. Periodontol 2000. 2003, 32: 11-23. 10.1046/j.0906-6713.2002.03202.x.View ArticlePubMedGoogle Scholar
- Briasoulis A, Agarwal V, Messerli FH: Alcohol consumption and the risk of hypertension in men and women: a systematic review and meta-analysis. J Clin Hypertens (Greenwich). 2012, 14: 792-798. 10.1111/jch.12008.View ArticleGoogle Scholar
- Reinert DF, Allen JP: The Alcohol Use Disorders Identification Test (AUDIT): a review of recent research. Alcohol Clin Exp Res. 2002, 26: 272-279. 10.1111/j.1530-0277.2002.tb02534.x.View ArticlePubMedGoogle Scholar
- Sheron N, Moore M, O’Brien W, Harris S, Roderick P: Feasibility of detection and intervention for alcohol-related liver disease in the community: the Alcohol and Liver Disease Detection study (ALDDeS). Br J Gen Pract. 2013, 63: e698-e705. 10.3399/bjgp13X673711.View ArticlePubMedPubMed CentralGoogle Scholar
- Allen JP, Reinert DF, Volk RJ: The Alcohol Use Disorders Identification Test: an aid to recognition of alcohol problems in primary care patients. Prev Med. 2001, 33: 428-433. 10.1006/pmed.2001.0910.View ArticlePubMedGoogle Scholar
- Lages EJ, Costa FO, Lages EM, Lages EJ, Costa FO, Lages EM, Cota LO, Cortelli SC, Nobre-Franco GC, Cyrino RM, Cortelli JR: Risk variables in the association between frequency of alcohol consumption and periodontitis. J Clin Periodontol. 2012, 39: 115-122. 10.1111/j.1600-051X.2011.01809.x.View ArticlePubMedGoogle Scholar
- Kwon YE, Ha JE, Paik DI, Jin BH, Bae KH: The relationship between periodontitis and metabolic syndrome among a Korean nationally representative sample of adults. J Clin Periodontol. 2011, 38: 781-786. 10.1111/j.1600-051X.2011.01756.x.View ArticlePubMedGoogle Scholar
- Kingman A, Albandar JM: Methodological aspects of epidemiological studies of periodontal diseases. Periodontol 2000. 2002, 29: 11-30. 10.1034/j.1600-0757.2002.290102.x.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6831/14/73/prepub
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