HbA1c Levels and Oral Candida albicans Burden in Patients with Type 2 Diabetes Mellitus

Authors

  • Aima Insana Medical Laboratory Technology Poltekkes Kemenkes Banjarmasin, Indonesia
  • Neni Oktiyani Medical Laboratory Technology Poltekkes Kemenkes Banjarmasin, Indonesia
  • Ricko Dharmadi Utama Medical Laboratory Technology Poltekkes Kemenkes Banjarmasin, Indonesia https://orcid.org/0000-0002-1682-7243

DOI:

https://doi.org/10.35916/thmr.v8i2.160

Keywords:

Type 2 Diabetes Mellitus, HbA1c, Oral Candidiasis, Candida albicans, Glycemic Control

Abstract

Diabetes Mellitus (DM) is a chronic metabolic disorder characterized by hyperglycemia, which may increase salivary glucose levels and facilitate the growth of Candida albicans in the oral cavity. Glycated hemoglobin (HbA1c) is a widely used indicator of long-term glycemic control and may be associated with oral Candida colonization in patients with Type 2 Diabetes Mellitus. This study aimed to analyze the association between HbA1c levels and Candida albicans colony counts in oral-rinse specimens among patients with Type 2 Diabetes Mellitus. This analytical observational study used a cross-sectional design and included 33 patients with Type 2 Diabetes Mellitus at the Posyandu of Puskesmas Guntung Manggis, Banjarbaru, South Kalimantan, using total sampling. Data collection included blood glucose, triglyceride, and HbA1c measurements, as well as identifying and quantifying Candida albicans in oral-rinse specimens using CHROMagar and colony-forming unit (CFU/mL) counts. We assessed data normality using the Shapiro-Wilk test, followed by Spearman's rank correlation analysis. Most respondents were female (60.6%) and aged 55–64 years (48.5%). A total of 63.6% of respondents had HbA1c levels in the diabetic category (?6.5%). Regarding presumptive Candida albicans colony counts, 12.1% of respondents had elevated counts (400–1000 CFU/mL), while 9.1% had a high Candida burden (>1000 CFU/mL). Spearman's rank correlation analysis demonstrated significant positive correlations between Candida albicans colony counts and blood glucose (r = 0.470, p = 0.006), triglyceride levels (r = 0.366, p = 0.036), and HbA1c levels (r = 0.382, p = 0.028). These findings indicate that higher HbA1c levels are associated with higher presumptive Candida albicans colony counts in oral-rinse specimens among patients with Type 2 Diabetes Mellitus.

References

Agustina D, Chrisnawati RT, Chrismawaty BE, Wongsohardjono SB, Naritasari F, Sarasati A. Prevalence and identification of oral Candida species in patients with type 2 diabetes in Yogyakarta. Maj Kedokt Gigi Indones. 2023;9(1):57-66.

Duggal R, Goswami R, Xess I, Duggal I, Talwar A, Mathur VP. Prevalence of species-specific candidiasis and status of oral hygiene and dentition among diabetic patients: a hospital-based study. Indian J Dent Res. 2021;32(3):292–298.

Taylor M, Brizuela M, Raja A. Oral candidiasis. In: StatPearl. Treasure Island (FL): StatPearls Publishing; 2025 Jan. https://www.ncbi.nlm.nih.gov/books/NBK545282/

Patel M. Oral cavity and Candida albicans: colonisation to the development of infection. Pathogens (Basel). 2022;11(3):335. doi:10.3390/pathogens11030335.

Kurniawan LB. HbA1c as a diabetes mellitus biomarker and its methods evolution. Indones J Clin Pathol Med Lab. 2024;30(2):191–196.

Weykamp C. HbA1c: a review of analytical and clinical aspects. Ann Lab Med. 2013;33:393-400. doi:10.3343/alm.2013.33.6.393.

Harahap RIM, Rostini T, Suraya N. Pemeriksaan laboratorium pada hemoglobin terglikasi (HbA1C): review standarisasi dan implementasi klinis. Action Res Lit. 2024;8(6).

Leena K, Huq MN, Ahmed R, Enam A, Rizwan AAM. Diabetes mellitus & its relation to oral manifestation: a review. World J Pharm Res. 2022;11(5):135–144.

Puspitasari DRZ, Makkadafi SP, Azahra S. Gambaran jamur Candida albicans pada saliva penderita DM tipe 2 di Puskesmas Harapan Baru Samarinda. J Ilmu Kedokt Kesehat. 2023;10(11):3273-3280.

Manihuruk FN, Gultom AG. Identification of Candida albicans in saliva of patients with type 2 diabetes mellitus at the Simalingkar Health Center, Medan City. J EduHealth. 2024;15(4):799–809.

American Diabetes Association Professional Practice Committee for Diabetes. 2. Diagnosis and classification of diabetes: Standards of Care in Diabetes—2026. Diabetes Care. 2026;49(Suppl 1):S27-S49. doi:10.2337/dc26-S002.

Wijerathna AAWM, Weerasekera WBMCRD, Jayawardene KLTD, Ratnapreya S, Bandara HMHN. Oral prevalence of Candida in adolescents on removable orthodontic appliance therapy at Dental Teaching Hospital, Peradeniya, Sri Lanka: a pilot study. Ceylon J Sci. 2024;53(4):471-475. doi:10.4038/cjs.v53i4.8354.

Epstein JB, Pearsall NN, Truelove EL. Quantitative relationships between Candida albicans in saliva and the clinical status of human subjects. J Clin Microbiol. 1980;12(3):475-476. doi:10.1128/jcm.12.3.475-476.1980.

Nadig SD, Ashwathappa DT, Manjunath M, Krishna S, Annaji AG, Shivaprakash PK. A relationship between salivary flow rates and Candida counts in patients with xerostomia. J Oral Maxillofac Pathol. 2017;21(2):316. doi:10.4103/jomfp.JOMFP_231_16.

CHROMagar. CHROMagar™ Candida: instructions for use [Internet]. Version 10.1. Paris: CHROMagar; 2024. cited 2026 Oct. https://www.chromagar.com/wp-content/uploads/2021/11/NT-EXT-001-V10.1.pdf

Aiello HQ, Santos FA, Silva MS, Lima GS. Immunosenescence and salivary immune profile changes in elderly patients with type 2 diabetes mellitus. J Appl Oral Sci. 2022;30:e20220112.

Al-Quraishy S, Al-Malki ES, Abdel-Gaber R. Hormonal influence on oral mucosal immunity and fungal susceptibility in postmenopausal diabetic females. Microb Pathog. 2023;174:105930.

Berbudi A, Rahmadika N, Tjahjadi AI, Ruslami R. Type 2 diabetes and its impact on the immune system. Curr Diabetes Rev. 2020;16(5):442-449. doi:10.2174/1573399815666191024085838.

Silva S, Negri M, Henriques M, Oliveira R, Williams DW, Azeredo J. Salivary glucose concentration and its role in Candida albicans adhesion in diabetic patients. Arch Oral Biol. 2021;124:105078.

Tsang PW, Bandara HM, Fong WP. Hypoglycemic state vs hyperglycemia in oral Candida morphogenesis and virulence expression. Front Microbiol. 2022;13:843105.

American Diabetes Association. Standards of Care in Diabetes—2024. Diabetes Care. 2024;47(Suppl 1):S1-S343.

Singh VP, Bali A, Singh N, Jaggi AS. Advanced glycation end products and RAGE axis in oral mucosal lesions of diabetic origin. Mol Cell Biochem. 2023;478(4):815-829.

Kumar S, Ranganathan K, Saraswathi TR. Mucosal barrier integrity and Candida colonization in uncontrolled type 2 diabetes. Oral Dis. 2022;28(6):1620–1628.

Sanyaolu A, Okorie C, Marinkovic A, Popovic S. Dyslipidemia and long-term metabolic complications in type 2 diabetes mellitus patients. Curr Diabetes Rev. 2023;19(3):e180522204981.

Preshaw PM, Taylor JJ. Salivary lipids, metabolic syndrome, and oral mucosal health. Periodontol 2000. 2022;89(1):112-125.

Dodds MW, Yeh CK, Johnson DA. Salivary alterations in type 2 (non-insulin-dependent) diabetes mellitus and hypertension. Community Dent Oral Epidemiol. 2000;28(5):373-381. doi:10.1034/j.1600-0528.2000.028005373.x.

Vila T, Sultan AS, Montelongo-Jauregui D, Jabra-Rizk MA. Oral candidiasis: a disease of opportunity. J Fungi (Basel). 2020;6(1):15. doi:10.3390/jof6010015.

Downloads

Published

31-08-2026

How to Cite

Insana, A., Oktiyani, N., & Utama, R. D. (2026). HbA1c Levels and Oral Candida albicans Burden in Patients with Type 2 Diabetes Mellitus. Tropical Health and Medical Research, 8(2), 129–139. https://doi.org/10.35916/thmr.v8i2.160

Most read articles by the same author(s)

<< < 1 2