Assessment of the association between the components of the metabolic syndrome and the pathology of dental hard tissues and inflammatory periodontal diseases
https://doi.org/10.36377/ET-0058
Abstract
AIM. Is to assess the interaction between the pathology of carious and non-carious dental hard tissues, inflammatory periodontal diseases and components of the metabolic syndrome (MS).
MATERIALS AND METHODS. A retrospective observational and comprehensive dental examination of 105 patients with MS has been performed. The complex of dental examination included analysis of complaints, anamnesis, assessment of the condition of dental hard tissues, and periodontal tissues. As a result of retrospective observational analysis, 3 clinical groups have been formed as follows: 2 main clinical groups with MS with impaired carbohydrate metabolism, and with type 2 diabetes mellitus, as well as a group with MS without impaired carbohydrate metabolism (experimental group).
RESULTS. The caries prevalence rate in patients of the 1st and 2nd main clinical groups according to WHO criteria is high, that is 92.5% and 97.3%, (р < 0.001), the average caries intensity level according to the DMF index (Decayed, Missing, Filled index) corresponds to the criterion of high and very high (< 0.001), there is a prevalence of increased abrasion in 76.3% and 51.0% (р < 0.05), hyperesthesia in 69.2% and 67.3%, wedge-shaped defects of hard tissues in 57.7% and 46.2% (р < 0.001), in 34.6% and 80.8% of cases there is a prevalence of chronic periodontitis (р < 0.001) as compared to the experimental group. In this category of patients, the median value of hygienic (SOHI / Simplified Oral Health Index) and periodontal indices of SBI, PI, periodontal pocket depth have been statistically and significantly different from the experimental group patients according to the Kruskal Wallis Test, р < 0.01.
CONCLUSIONS. Thus, in patients with metabolic syndrome with impaired carbohydrate metabolism and type 2 diabetes mellitus, the prevalence of carious and non-carious tooth hard tissue pathology and periodontal inflammatory diseases is observed among the main dental diseases. The data obtained require an interdisciplinary approach in the development and planning of early qualitative diagnostic and treatment and preventive interventions maneuvers in conjunction with a dentist, endocrinologist, and a therapist.
About the Authors
V. O. SeninaRussian Federation
Valeriya O. Senina – Postgraduate Student of the Department of Therapeutic Dentistry, Assistant of the Department of Surgical Dentistry
3 Lenin Str., Ufa 450008
Competing Interests:
The authors declare no conflict of interests
I. N. Usmanova
Russian Federation
Irina N. Usmanova – Dr. Sci. (Med.), Professor of the Department of Therapeutic Dentistry
3 Lenin Str., Ufa 450008
Competing Interests:
The authors declare no conflict of interests
I. A. Lakman
Russian Federation
Irina A. Lakman – Cand. Sci. (Eng.), Leading Researcher of the Central Research Laboratory; Head of the Scientific Laboratory for Research of SocioEconomic Problems of Regions
3 Lenin Str., Ufa 450008, Russian Federation
32 Zaki Validi Str., Ufa 450076
Competing Interests:
The authors declare no conflict of interests
L. P. Gerasimova
Russian Federation
Larisa P. Gerasimova – Dr. Sci. (Med.), Professor, Honored Doctor of the Сhief of the Department Therapeutic Dentistry
3 Lenin Str., Ufa 450008
Competing Interests:
The authors declare no conflict of interests
A. N. Ishmukhametova
Russian Federation
Amina N. Ishmukhametova – Cand. Sci. (Med.), Associate Professor of the Department of Internal Medicine and Clinical Psychology
3 Lenin Str., Ufa 450008
Competing Interests:
The authors declare no conflict of interests
N. A. Makarova
Russian Federation
Natalia А. Makarova – Cand. Sci. (Med.), Assistant of the Department of Therapeutic Dentistry
49 Butlerova Str., Kazan 420012
Competing Interests:
The authors declare no conflict of interests
V. A. Berezin
Russian Federation
Veniamin А. Berezin – Cand. Sci. (Med.), Assistant of the Department of Oral and Maxillofacial Surgery and Surgical Dentistry
49 Butlerova Str., Kazan 420012
Competing Interests:
The authors declare no conflict of interests
References
1. Dedov I.I., Shestakova M.V., Vikulova O.K., Zheleznyakova A.V., Isakov M.A., Sazonova D.V., Mokrysheva N.G. Diabetes mellitus in the Russian Federation: dynamics of epidemiological indicators according to the Federal Register of Diabetes Mellitus for the period 2010–2022. Diabetes Mellitus. 2023;26(2):104–123. https://doi.org/10.14341/DM13035
2. Moradpour F., Karimi Z., Fatemi Z., Moradi Y., Khosravi M.R., Shokri A., Karimzadeh M. Prevalence of metabolic syndrome and its association with oral health: First results from the Kurdish cohort study. Health Sci Rep. 2023;6(10):e1602. https://doi.org/10.1002/hsr2.1602
3. Noubiap J.J., Nansseu J.R., Lontchi-Yimagou E., Nkeck J.R., Nyaga U.F., Ngouo A.T. et al. Geographic distribution of metabolic syndrome and its components in the general adult population: A meta-analysis of global data from 28 million individuals. Diabetes Res Clin Pract. 2022;188:109924. https://doi.org/10.1016/j.diabres.2022.109924
4. Magliano D.J., Boyko E.J., IDF Diabetes Atlas 10th edition scientific committee. IDF Diabetes Atlas. 10th ed. Brussels: International Diabetes Federation; 2021.
5. Dedov I.I., Shestakova M.V., Vikulova O.K., Isakov M.А., Zheleznyakova A.V. Atlas of Diabetes Register in Russian Federation, status 2018. Diabetes Mellitus. 2019;22(2S):4–61. (In Russ.) https://doi.org/10.14341/DM12208
6. Adachi N., Kobayashi Y. One-year follow-up study on associations between dental caries, periodontitis, and metabolic syndrome. J Oral Sci. 2020;62(1):52–56. https://doi.org/10.2334/josnusd.18-0251
7. Cao X., Wang D., Zhou J., Yuan H., Chen Z. Relationship between dental caries and metabolic syndrome among 13 998 middle-aged urban Chinese. J Diabetes. 2017;9(4):378–385. https://doi.org/10.1111/1753-0407.12424
8. Aizenbud I., Wilensky A., Almoznino G. Periodontal disease and its association with metabolic syndrome-a comprehensive review. Int J Mol Sci. 2023;24(16):13011. https://doi.org/10.3390/ijms241613011
9. Sabharwal A., Stellrecht E., Scannapieco F.A. Associations between dental caries and systemic diseases: a scoping review. BMC Oral Health. 2021;21(1):472. https://doi.org/10.1186/s12903-021-01803-w
10. Chen H., Hill R., Baysan A. Systematic review on dental caries preventive and managing strategies among type 2 diabetic patients. Front Oral Health. 2022;3:998171. https://doi.org/10.3389/froh.2022.998171
11. Latti B.R., Kalburge J.V., Birajdar S.B., Latti R.G. Evaluation of relationship between dental caries, diabetes mellitus and oral microbiota in diabetics. J Oral Maxillofac Pathol. 2018;22(2):282. https://doi.org/10.4103/jomfp.JOMFP_163_16
12. Preshaw P.M., Bissett S.M. Periodontitis and diabetes. Br Dent J. 2019;227(7):577–584. https://doi.org/10.1038/s41415-019-0794-5
13. Takeda K., Mizutani K., Minami I., Kido D., Mikami R., Konuma K. et al. Association of periodontal pocket area with type 2 diabetes and obesity: a cross-sectional study. BMJ Open Diabetes Res Care. 2021;9(1):e002139. https://doi.org/10.1136/bmjdrc-2021-002139
14. Winning L., Patterson C.C., Neville C.E., Kee F., Linden G.J. Periodontitis and incident type 2 diabetes: a prospective cohort study. J Clin Periodontol. 2017;44(3):266–274. https://doi.org/10.1111/jcpe.12691
15. Isamulaeva A.Z., Medveditskova A.I., Bashtovoy A.A. An integrated approach to reducing hyperesthesia of teeth in patients with underlying somatic pathology. Stomatology. 2022;101(6):18–21. (In Russ.) https://doi.org/10.17116/stomat202210106118
16. Dedov I.I., Mokrysheva N.G., Mel’nichenko G.A., Troshina E.A., Mazurina N.V., Ershova E.V. et al. Obesity. Clinical guidelines. Consilium Medicum. 2021;23(4):311–325. Available at: https://consilium.orscience.ru/2075-1753/article/download/95436/pdf (accessed: 01.11.2024).
17. Dedov I.I., Shestakova M.V., Melnichenko G.A., Mazurina N.V., Andreeva E.N., Bondarenko I.Z. et al. Interdisciplinary clinical practice guidelines “Management of obesity and its comorbidities”. Obesity and Metabolism. 2021;18(1):5–99. (In Russ.) https://doi.org/10.14341/omet12714
18. Dedov I.I., Shestakova M.V., Mayorov A.Yu., Mokrysheva N.G., Andreeva E.N., Bezlepkina O.B. et al. Standards of Specialized Diabetes Care / Edited by I.I. Dedov, M.V. Shestakova, A.Yu. Mayorov. 11th Edition. Diabetes Mellitus. 2023;26(2S):1–157. (In Russ.) https://doi.org/10.14341/DM13042
19. Esfanjani M.T., Gilani N., Esfanjani A.T., Nourizadeh A.M., Faramarzi E., Hekmatfar S. Are oral health behaviors associated with metabolic syndrome in the Azar cohort population? BMC Oral Health. 2023;23(1):370. https://doi.org/10.1186/s12903-023-03003-0
20. Almusawi M.A., Gosadi I., Abidia R., Almasawi M., Khan H.A. Potential risk factors for dental caries in Type 2 diabetic patients. Int J Dent Hyg. 2018;16(4):467–475. https://doi.org/10.1111/idh.12346
21. Song I.S., Han K., Park Y.M., Ryu J.J., Park J.B. Type 2 diabetes as a risk indicator for dental caries in Korean adults: the 2011–2012 Korea national health and nutrition examination survey. Community Dent Health. 2017;34(3):169–175. https://doi.org/10.1922/CDH_4113Song07
22. Papapanou P.N., Sanz M., Buduneli N., Dietrich T., Feres M., Fine D.H. et al. Periodontitis: Consensus report of workgroup 2 of the 2017 World Workshop on on the Classification of Periodontal and PeriImplant Diseases and Conditions. J Clin Periodontol. 2018;45(Suppl. 20):S162–S170. https://doi.org/10.1111/jcpe.12946
23. Pham T. The association between periodontal disease severity and metabolic syndrome in Vietnamese patients. Int J Dent Hyg. 2018;16(4):484–491. https://doi.org/10.1111/idh.12350
24. Kaura Parbhakar K., Rosella L.C., Singhal S., Quiñonez C.R. Risk of complications among diabetics self-reporting oral health status in Canada: A population-based cohort study. PLoS ONE. 2020;15(1):e0218056. https://doi.org/10.1371/journal.pone.0218056
25. Hlushchenko T.A., Batig V.M., Borysenko A.V., Tokar O.M., Batih I.V., Vynogradova O.M., BoychukTovsta O.G. Prevalence and intensity of periodontal disease in individuals with metabolic syndrome. J Med Life. 2020;13(3):289–292. https://doi.org/10.25122/jml-2020-0073
26. Gomes-Filho I.S., Balinha I.d.S.C.E., da Cruz S.S., Trindade S.C., Cerqueira E.d.M.M., Passos-Soares J.d.S. Moderate and severe periodontitis are positively associated with metabolic syndrome. Clin Oral Invest. 2021;25(6):3719–3727. https://doi.org/10.1007/s00784-020-03699-2
27. Singh M., Bains V.K., Jhingran R., Srivastava R., Madan R., Maurya S.C., Rizvi I. Prevalence of periodontal disease in Type 2 diabetes mellitus patients: A cross-sectional study. Contemp Clin Dent. 2019;10(2):349–357. https://doi.org/10.4103/ccd.ccd_652_18
28. Wu C.-Z., Yuan Y.-H., Liu H.-H., Li S.-S., Zhang B.-W., Chen W. et al. Epidemiologic relationship between periodontitis and type 2 diabetes mellitus. BMC Oral Health. 2020;20:204. https://doi.org/10.1186/s12903-020-01180-w
29. Fernandez-Gutierrez M.M., Imangaliyev S., Prodan A., Loos B.G., Keijser B.J.F., Kleerebezem M. A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility. Sci Rep. 2020;10(1):3008. https://doi.org/10.1038/s41598-020-59988-z
30. Xavier I., Botelho J., Machado V., Rua J., Delgado A.S., Mendes J.J. Association between hypertension and chronic periodontitis in a Portuguese population. Ann Med. 2019;51(Suppl. 1):132. https://doi.org/10.1080/078 53890.2018.1561972
31. Lamster I.B., Pagan M. Periodontal disease and the metabolic syndrome. Int Dent J. 2017;67(2):67–77. https://doi.org/10.1111/idj.12264
Review
For citations:
Senina V.O., Usmanova I.N., Lakman I.A., Gerasimova L.P., Ishmukhametova A.N., Makarova N.A., Berezin V.A. Assessment of the association between the components of the metabolic syndrome and the pathology of dental hard tissues and inflammatory periodontal diseases. Endodontics Today. 2024;22(4):422–430. (In Russ.) https://doi.org/10.36377/ET-0058