Association of periodontitis stages with glycemic control in adults with and without type 2 diabetes mellitus: a cross-sectional study
DOI:
https://doi.org/10.1590/1678-7765-2026-0178Keywords:
Periodontitis, Diabetes mellitus, Glycated hemoglobin, DyslipidemiaAbstract
Objective: To investigate associations among periodontal parameters, glycated hemoglobin (HbA1c), and metabolic parameters in adults with and without type 2 diabetes mellitus (T2D). Methodology: A cross-sectional study included 74 adults diagnosed with periodontitis according to the current periodontal classification of 2018. Participants underwent a full-mouth periodontal examination, laboratory assessment, and Body Mass Index (BMI). Periodontitis was categorized into Stages I/II and Stages III/IV. HbA1c, lipid profile, high-sensitivity C-reactive protein (CRP), and insulin resistance (HOMA-IR) were assessed. Periodontal inflammatory burden was quantified using the Periodontal Inflamed Surface Area (PISA). Non-parametric tests and Spearman correlation analyses were performed, stratified by diabetes status (α=5%). Results: Individuals with advanced periodontitis (Stages III/IV) had significantly higher HbA1c levels (6.8% vs. 5.8%; p=0.007), higher triglyceride concentrations (142.0 vs. 100.5 mg/dL; p=0.016), and lower HDL-cholesterol levels (46.0 vs. 52.0 mg/dL; p=0.012) than those in Stages I/II. Poor glycemic control (HbA1c >8.5%) and T2D duration ≥10 years were significantly associated with advanced stages (p<0.05). No significant differences were observed for BMI, LDL, total cholesterol (TC), CRP, or HOMA-IR between groups. In adults with T2D, PISA correlated positively with TC and LDL-cholesterol, whereas in non-diabetic individuals, PISA was associated primarily with triglycerides. Conclusions: Advanced periodontitis was associated with poorer glycemic control and a more atherogenic lipid profile, particularly characterized by elevated triglycerides and reduced HDL-cholesterol. The findings support periodontitis as a potential marker of systemic metabolic dysregulation and reinforce the importance of integrating periodontal care into cardiometabolic risk management strategies.
Downloads
References
1- Ahmad E, Lim S, Lamptey R, Webb DR, Davies MJ. Type 2 diabetes. Lancet. 2022;400(10365):1803-20. doi: 10.1016/S0140-6736(22)01655-5
» https://doi.org/10.1016/S0140-6736(22)01655-5
2- Basdorf P, Kocher T, Baumeister SE, Pink C, Budde K, Petersmann A, et al. Periodontitis adversely affects lipoprotein subfractions: results from the cohort study SHIP-TREND. Diabetes Metab. 2024;50(6):101584. doi: 10.1016/j.diabet.2024.101584
» https://doi.org/10.1016/j.diabet.2024.101584
3- Song TJ, Kim JW, Kim J. Oral health and changes in lipid profile: a nationwide cohort study. J Clin Periodontol. 2020;47(12):1437-45. doi: 10.1111/jcpe.13373
» https://doi.org/10.1111/jcpe.13373
4- Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28(7):412-9. doi: 10.1007/BF00280883
» https://doi.org/10.1007/BF00280883
5- Preshaw PM, Alba AL, Herrera D, Jepsen S, Konstantinidis A, Makrilakis K, et al. Periodontitis and diabetes: a two-way relationship. Diabetologia. 2012;55(1):21-31. doi: 10.1007/s00125-011-2342-y
» https://doi.org/10.1007/s00125-011-2342-y
6- Graves DT, Ding Z, Yang Y. The impact of diabetes on periodontal diseases. Periodontol 2000. 2020;82(1):214-24. doi: 10.1111/prd.12318
» https://doi.org/10.1111/prd.12318
7- Graves DT, Levine MA, Aldosary S, Demmer RT. Understanding the periodontitis-diabetes linkage: mechanisms and evidence. J Dent Res. 2026;105(1):21-30. doi: 10.1177/00220345251388340
» https://doi.org/10.1177/00220345251388340
8- Papapanou PN, Sanz M, Buduneli N, Dietrich T, Feres M, Fine DH, et al. Periodontitis: consensus report of workgroup 2 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. J Periodontol. 2018;89 Suppl 1:S173-S182. doi: 10.1002/JPER.17-0721
» https://doi.org/10.1002/JPER.17-0721
9- Nepomuceno R, Pigossi SC, Finoti LS, Orrico SR, Cirelli JA, Barros SP, et al. Serum lipid levels in patients with periodontal disease: a meta-analysis and meta-regression. J Clin Periodontol. 2017;44(12):1192-207. doi: 10.1111/jcpe.12792
» https://doi.org/10.1111/jcpe.12792
10- Tran AH, Zaidi AH, Bolger AF, Del Brutto OH, Hegde R, Patton LL, et al. Periodontal disease and atherosclerotic cardiovascular disease: a scientific statement from the American Heart Association. Circulation. 2026;153(6):e73-e88. doi: 10.1161/CIR.0000000000001390
» https://doi.org/10.1161/CIR.0000000000001390
11- Gomes-Filho IS, Santos PN, Cruz SS, Figueiredo AC, Trindade SC, Ladeia AM, et al. Periodontitis and its higher levels of severity are associated with the triglyceride/high density lipoprotein cholesterol ratio. J Periodontol. 2021;92(11):1509–21. doi: 10.1002/JPER.21-0004
» https://doi.org/10.1002/JPER.21-0004
12- Tonetti MS, Greenwell H, Kornman KS. Staging and grading of periodontitis: framework and proposal of a new classification and case definition. J Periodontol. 2018;89(Suppl 1) S159-S172. doi: 10.1002/JPER.18-0006
» https://doi.org/10.1002/JPER.18-0006
13- Nesse W, Abbas F, van der Ploeg I, Spijkervet FK, Dijkstra PU, Vissink A. Periodontal inflamed surface area: quantifying inflammatory burden. J Clin Periodontol. 2008;35(8):668–73. doi: 10.1111/j.1600-051X.2008.01249.x
» https://doi.org/10.1111/j.1600-051X.2008.01249.x
14- Susanto H, Nesse W, Dijkstra PU, Hoedemaker E, van Reenen YH, Agustina D, et al. Periodontal inflamed surface area and C-reactive protein as predictors of HbA1c: a study in Indonesia. Clin Oral Investig. 2012;16(4):1237-42. doi: 10.1007/s00784-011-0621-0
» https://doi.org/10.1007/s00784-011-0621-0
15- Ni Riordain R, Glick M, Al Mashhadani SSA, Aravamudhan K, Barrow J, Cole D, et al. Developing a standard set of patient-centred outcomes for adult oral health: an international, cross-disciplinary consensus. Int Dent J. 2021;71(1):40-52. doi: 10.1111/idj.12604
» https://doi.org/10.1111/idj.12604
16- Tomar SL, Asma S. Smoking-attributable periodontitis in the United States: findings from NHANES III. J Periodontol. 2000;71(5):743-51. doi: 10.1902/jop.2000.71.5.743
» https://doi.org/10.1902/jop.2000.71.5.743
17- Fleiss JL, Levin B, Paik MC. Statistical methods for rates and proportions. 3rd ed. Hoboken: Wiley; 2003. doi: 10.1002/0471445428
» https://doi.org/10.1002/0471445428
18- Banjar A, Alyafi R, AlGhamdi A, Assaggaf M, Almarghlani A, Hassan S, et al. The relationship between glycated hemoglobin level and the stage of periodontitis in individuals without diabetes. PLoS One. 2023;18(1). doi: 10.1371/journal.pone.0279755
» https://doi.org/10.1371/journal.pone.0279755
19- Alhassani AA. The influence of periodontitis case definition on the association between periodontal disease and glycaemic status. Community Dent Oral Epidemiol. 2023;51(6):1100-8. doi: 10.1111/cdoe.12839
» https://doi.org/10.1111/cdoe.12839
20- Preshaw PM, Bissett SM. Periodontitis and diabetes. Br Dent J. 2019;227(7):577-84. doi: 10.1038/s41415-019-0794-5
» https://doi.org/10.1038/s41415-019-0794-5
21- Dong YL, Lin H, Wen T, Guo ZL. Multi-dimensional role of AGEs in periodontitis: from matrix remodeling to neuro-immune crosstalk. Front Immunol. 2025;16:1643685. doi: 10.3389/fimmu.2025.1643685
» https://doi.org/10.3389/fimmu.2025.1643685
22- Isola G, Matarese G, Ramaglia L, Pedullà E, Rapisarda E, Iorio-Siciliano V. Association between periodontitis and glycosylated haemoglobin before diabetes onset: a cross-sectional study. Clin Oral Investig. 2020;24(8):2799-808. doi: 10.1007/s00784-019-03143-0
» https://doi.org/10.1007/s00784-019-03143-0
23- Demmer RT, Desvarieux M, Holtfreter B, Jacobs DR Jr, Wallaschofski H, Nauck M, et al. Periodontal status and A1C change: longitudinal results from the Study of Health in Pomerania (SHIP). Diabetes Care. 2010;33(5):1037-43. doi: 10.2337/dc09-1778
» https://doi.org/10.2337/dc09-1778
24- Abu-Shawish G, Betsy J, Anil S. Is obesity a risk factor for periodontal disease in adults? A systematic review. Int J Environ Res Public Health. 2022;19(19):12684. doi: 10.3390/ijerph191912684
» https://doi.org/10.3390/ijerph191912684
25- Thouvenot K, Serrat F, Lenclume V, Doussiet E, Belda E, Taïlé J, et al. Periodontitis in patients with severe obesity: from the oral microbiota to the gut microbiome. FASEB J. 2026;40(9):e71828. doi: 10.1096/fj.202600054R
» https://doi.org/10.1096/fj.202600054R
26- Xu J, Duan X. Association between periodontitis and hyperlipidaemia: a systematic review and meta-analysis. Clin Exp Pharmacol Physiol. 2020;47(11):1861-73. doi: 10.1111/1440-1681.13372
» https://doi.org/10.1111/1440-1681.13372
27- Ehteshami A, Shirban F, Bagherniya M, Sathyapalan T, Jamialahmadi T, Sahebkar A. The association between high-density lipoproteins and periodontitis. Curr Med Chem. 2024;31(39):6407-28. doi: 10.2174/0929867331666230726140736
» https://doi.org/10.2174/0929867331666230726140736
28- Gupta V, Dawar A, Das SK, Yadav VS, Nalwa V, Haidrus R, et al. Cardiovascular biomarkers in periodontitis: a systematic review and meta-analysis. Oral Dis. 2026;32(2):278-87. doi: 10.1111/odi.70084
» https://doi.org/10.1111/odi.70084
29- Singer RE, Moss K, Kim SJ, Beck JD, Offenbacher S. Oxidative stress and IgG antibody modify periodontitis-CRP association. J Dent Res. 2015;94(12):1698-705. doi: 10.1177/0022034515602693
» https://doi.org/10.1177/0022034515602693
30- Zhou X, Zhang W, Liu X, Zhang W, Li Y. Interrelationship between diabetes and periodontitis: role of hyperlipidemia. Arch Oral Biol. 2015;60(4):667-74. doi: 10.1016/j.archoralbio.2014.11.008
» https://doi.org/10.1016/j.archoralbio.2014.11.008
31- Zhang D, Zhao C, Liu Z, Ding Y, Li W, Yang H, et al. Relationship between periodontal status and dyslipidemia in patients with type 2 diabetic nephropathy and chronic periodontitis: a cross-sectional study. J Periodontal Res. 2022;57(5):969-76. doi: 10.1111/jre.13033
» https://doi.org/10.1111/jre.13033
32- Iwashita M, Seto-Tetsuo F, Yamashita A. Associations between periodontal disease-induced immune cell activation and energy metabolism. Front Immunol. 2026;17:1773346. doi: 10.3389/fimmu.2026.1773346
» https://doi.org/10.3389/fimmu.2026.1773346
33- Miki K, Kitamura M, Hatta K, Kamide K, Gondo Y, Yamashita M, et al. Periodontal inflamed surface area is associated with hs-CRP in septuagenarian Japanese adults in cross-sectional findings from the SONIC study. Sci Rep. 2021;11(1):14436. doi: 10.1038/s41598-021-93872-8
» https://doi.org/10.1038/s41598-021-93872-8
34- Leite FR, Nascimento GG, Scheutz F, López R. Effect of smoking on periodontitis: a systematic review and meta-regression. Am J Prev Med. 2018;54(6):831-41. doi: 10.1016/j.amepre.2018.02.014
» https://doi.org/10.1016/j.amepre.2018.02.014
35- Borgnakke WS, Ylöstalo PV, Taylor GW, Genco RJ. Effect of periodontal disease on diabetes: systematic review of epidemiologic observational evidence. J Clin Periodontol. 2013;40(Suppl 14):S135-52. doi: 10.1111/jcpe.12080
Downloads
Published
Issue
Section
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Todo o conteúdo do periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons do tipo atribuição CC-BY.