Dental and Medical Problems

Dent Med Probl
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ISSN 2300-9020 (online)
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Dental and Medical Problems

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doi: 10.17219/dmp/127873

Publication type: original article

Language: English

License: Creative Commons Attribution 3.0 Unported (CC BY 3.0)

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Clinical condition of the oral cavity in overweight and obese patients

Katarzyna Deszczyńska1,A,B,C,D,E, Renata Górska2,A,E,F, Anna Haładyj2,B,D

1 Department of Descriptive and Clinical Anatomy, Center of Biostructure Research, Medical University of Warsaw, Poland

2 Department of Periodontology and Oral Diseases, Faculty of Dentistry, Medical University of Warsaw, Poland

Abstract

Background. The increasing prevalence of both obesity and periodontal disease in adults has raised interest among researchers in a correlation between these conditions. Obesity is caused by a poorly balanced diet, rich in sugars, that leads to the accumulation of excessive amounts of plaque, which results in the development of gingivitis, periodontitis and caries. It is known that there is a correlation between these 2 disease entities, but the mechanisms of the interaction have not been explored to date. Thus, attempts to address this research question seem justified.
Objectives. The aim of the study was to compare selected parameters of dental and periodontal health as well as the oral hygiene status between overweight/obese adults and a control group. Additionally, eating habits and other factors affecting obesity in adults were examined in comparison with the control group on the basis of a self-developed questionnaire.
Material and Methods. The study included 120 adult patients (men and women), aged 19–55 years, divided into a study group of 60 overweight/obese individuals and a control group of 60 individuals with a normal weight based on the body mass index (BMI). The study involved anthropometric measurements (BMI, waist circumference – WC and hip circumference – HC) and dental examination, including dental caries examination (the decayed, missing and filled teeth index – DMF), oral hygiene assessment (the approximal plaque index – API) and periodontal tissue examination (pocket depth – PD, clinical attachment level – CAL, bleeding on probing – BOP, and the community periodontal index – CPI). Sociomedical examination was performed taking into account dietary and hygienic habits.
Results. The group with BMI ≥ 25 kg/m2 was found to have worse parameters of periodontal health and unsatisfactory oral hygiene status as compared to the control group. This group also presented lower regularity of eating meals and a higher rate of sweets consumption.
Conclusion. Lower regularity of eating meals and higher sweets consumption, combined with poor hygiene habits, are reflected in increased rates of gum inflammation and plaque accumulation as well as worsened periodontal tissue status. A positive correlation between periodontal disease and BMI points to the need to arrange for periodontal disease prevention and treatment among overweight and obese patients.

Key words

diet, overweight, periodontal disease, oral hygiene

References (23)

  1. Albandar JM. Underestimation of periodontitis in NHANES surveys. J Periodontol. 2011;82(3):337–341. doi:10.1902/jop.2011.100638
  2. Murray H, Clarke M, Locker D, Kay EJ. Reasons for tooth extractions in dental practices in Ontario, Canada according to tooth type. Int Dent J. 1997;47(1):3–8. doi:10.1111/j.1875-595x.1997.tb00670.x
  3. Phipps KR, Stevens VJ. Relative contribution of caries and periodontal disease in adult tooth loss for an HMO dental population. J Public Health Dent. 1995;55(4):250–252. doi:10.1111/j.1752-7325.1995.tb02377.x
  4. Lehmann-Kalata A, Surdacka A, Ciężka-Hsiao E. Obesity and its exponents in the oral cavity – a literature review [in Polish]. Dent Forum. 2013;41(2):57–61.
  5. Ainamo J, Barmes D, Beargie G, Cutress T, Martin J, Sardo-Infirri I. Development of the World Health Organization (WHO) community periodontal index of treatment needs (CPITN). Int Dent J. 1982;32(3):281–291.
  6. Suvan J, Petrie A, Moles DR, et al. Body mass index as a predictive factor of periodontal therapy outcomes. J Dent Res. 2014;93(1):49–54. doi:10.1177/0022034513511084
  7. Saito T, Shimazaki Y, Koga T, Tsuzuki M, Ohshima A. Relationship between upper body obesity and periodontitis. J Dent Res. 2001;80(7):1631–1636. doi:10.1177/00220345010800070701
  8. Saito T, Murakami M, Shimazaki Y, Matsumoto S, Yamashita Y. The extent of alveolar bone loss is associated with impaired glucose tolerance in Japanese men. J Periodontol. 2006;77(3):392–397. doi:10.1902/jop.2006.050061
  9. Wood N, Johnson RB, Streckfus CF. Comparison of body composition and periodontal disease using nutritional assessment technique: Third National Health and Nutrition Examination Survey (NHANES III). J Clin Periodontol. 2003;30(4):321–327. doi:10.1034/j.1600-051x.2003.00353.x
  10. Linden G, Patterson C, Evans A, Kee F. Obesity and periodontitis in 60–70-year-old men. J Clin Periodontol. 2007;34(6):461–466. doi:10.1111/j.1600-051X.2007.01075.x
  11. Chaffee BW, Weston SJ. Association between chronic periodontal disease and obesity: A systematic review and meta-analysis. J Periodontol. 2010;81(12):1708–1724. doi:10.1902/jop.2010.100321
  12. Balli U, Ongoz Dede F, Bozkurt Dogan S, Gulsoy Z, Sertoglu E. Chemerin and interleukin-6 levels in obese individuals following periodontal treatment. Oral Dis. 2016;22(7):673–680. doi:10.1111/odi.12520
  13. Pejcic A, Mirkovic D, Minic I, Stojanovic M. The association between periodontal disease and obesity among middle-aged adults periodontitis and obesity. J Metabolic Synd. 2016;5(3):208–213. doi:10.4172/2167-0943.1000208
  14. Nishida N, Tanaka M, Hayashi N, et al. Determination of smoking and obesity as periodontitis risks using the classification and regression tree method. J Periodontol. 2005;76(6):923–928. doi:10.1902/jop.2005.76.6.923
  15. Dalla Vecchia CF, Susin C, Rösing CK, Oppermann RV, Albandar JM. Overweight and obesity as risk indicator for periodontitis in adults. J Periodontol. 2005;76(10):1721–1728. doi:10.1902/jop.2005.76.10.1721
  16. Khader YS, Bawadi HA, Haroun TF, Alomari M, Tayyem RF. The association between periodontal disease and obesity among adults in Jordan. J Clin Periodontol. 2009;36(1):18–24. doi:10.1111/j.1600-051X.2008.01345.x
  17. Kongstad J, Hvidtfeldt UA, Grønbaek M, Stoltze K, Holmstrup P. The relationship between body mass index and periodontitis in the Copenhagen City Heart Study. J Periodontol. 2009;80(8):1246–1253. doi:10.1902/jop.2009.080559
  18. Górska R, Pietruska M, Dembowska E, Wysokińska-Miszczuk J, Włosowicz M, Konopka T. Prevalence of periodontal diseases in 35–44 year-olds in the large urban agglomerations [in Polish]. Dent Med Probl. 2012;49(1):19–27.
  19. Konopka T, Matuszewska A, Chrzęszczyk D, Zawada Ł. Body mass index and selected periodontal clinical parameters [in Polish]. Dent Med Probl. 2011;48(2):189–197.
  20. Touger-Decker R, Mobley CC; American Dietetic Association. Position of the American Dietetic Association: Oral health and nutrition. J Am Diet Assoc. 2007;107(8):1418–1428. doi:10.1016/j.jada.2007.06.003
  21. Yudkin J. Dental decay is preventable: Why not prevented? Br Dent J. 1969;127(9):425–429.
  22. Prpić J, Kuis D, Glazar I, Ribarić SP. Association of obesity with periodontitis, tooth loss and oral hygiene in non-smoking adults. Cent Eur J Public Health. 2013;21(4):196–201. doi:10.21101/cejph.a3829
  23. Hujoel PP, Cunha-Cruz J, Kressin NR. Spurious association in oral epidemiological research: The case of dental flossing and obesity. J Clin Periodontol. 2006;33(8):520–523. doi:10.1111/j.1600-051X.2006.00954.x