Ukr.Biochem.J. 2026; Volume 98, Issue 3, May-Jun, pp. 76-82

doi: https://doi.org/10.15407/ubj98.03.076

Leukocyte telomere length and clinical characteristics in patients with type 2 diabetes mellitus with and without chronic kidney disease

Y. E. Rebrova1,2,3*, Y. A. Saienko1,2, K. K. Midlovets1, B. M. Mankovsky1,3

1SI “D.F. Chebotarev Institute of Gerontology, National Academy
of Medical Sciences of Ukraine”, Kyiv;
2SI “Center for Cardiology and Cardiac Surgery of the Ministry
f Health of Ukraine”, Kyiv;
3P.L. Shupyk National University of Health Care of Ukraine, Kyiv;
*e-mail: yaninarebr@gmail.com

Received: 05 January 2026; Revised: 19 March 2026;
Accepted: 29 May 2026; Available on-line: 18 June 2026

Background. Telomeric mechanisms are considered important contributors to chronic kidney disease progression in patients with type 2 diabetes mellitus, although data on telomere length in diabetic kidney disease remain limited. Objective. To evaluate the relationship between telomere length and clinical characteristics in patients with type 2 diabetes mellitus with and without chronic kidney disease. Methods. The study included 100 patients with T2DM, divided into two groups: 50 with and 50 without CKD. Routine clinical and biochemical blood tests were performed for all subjects. Leukocyte telomere length was assessed by quantitative real-time polymerase chain reaction following the method described by Cawthon. Results. T2DM patients with CKD were significantly older, had a longer duration of diabetes, exhibited significantly lower estimated glomerular filtration rate (eGFR), higher urine albumin-to-creatinine ratio and frequency of cardiovascular complications compared with non-CKD patients. No significant correlations were found between telomere length and age, eGFR, albuminuria, or cardiovascular desease in either group. In patients with type 2 diabetes mellitus chronic kidney disease was associated with higher frequency of pathologically short telomeres (20.8%) versus non-CKD patients (2.1%), suggesting accelerated cellular aging in CKD independent of chronological age. Conclusions. Shortened telomeres in patients with type 2 diabetes mellitus and chronic kidney disease may reflect accelerated cellular aging and could serve as an additional marker for biological risk stratification beyond traditional renal indicators.
Keywords: telomeres, type 2 diabetes mellitus, chronic kidney disease, cellular aging.

Keywords: , , ,


References:

  1. Kidney Disease: Improving Global Outcomes (KDIGO) Diabetes Work Group. KDIGO 2022 Clinical Practice Guideline for Diabetes Management in Chronic Kidney Disease. Kidney Int. 2022;102(5S):S1–127. PubMed, CrossRef
  2. Tang SCW, Yiu WH. Innate immunity in diabetic kidney disease. Nat Rev Nephrol. 2020;16(4):206-222. PubMed, CrossRef
  3. Forbes JM, Cooper ME. Mechanisms of diabetic complications. Physiol Rev. 2013;93(1):137-188. PubMed, CrossRef
  4. Saienko YA, Krasnenkov DS, Midlovets KK, Korcheva VV, Rebrova YE, Yepishina DD, Mankovsky BM. Polymorphism of the angiotensin-converting enzyme (ACE) gene in individuals with type 2 diabetes and chronic kidney disease. Fiziol Zh. 2025;71(3):37-43. CrossRef
  5. Ortiz A, Sanchez-Niño MD, Izquierdo MC, Martin-Cleary C, Garcia-Bermejo L, Moreno JA, Ruiz-Ortega M, Draibe J, Cruzado JM, Garcia-Gonzalez MA, Lopez-Novoa JM, Soler MJ, Sanz AB. Translational value of animal models of kidney failure. Eur J Pharmacol. 2015;759:205-220. PubMed, CrossRef
  6. D’Mello MJ, Ross SA, Briel M, Anand SS, Gerstein H, Paré G. Association between shortened leukocyte telomere length and cardiometabolic outcomes: systematic review and meta-analysis. Circ Cardiovasc Genet. 2015;8(1):82-90. PubMed, CrossRef
  7. Blackburn EH. Switching and signaling at the telomere. Cell. 2001;106(6):661-673. PubMed, CrossRef
  8. Fyhrquist F, Saijonmaa O. Telomere length and cardiovascular aging. Ann Med. 2012;44(Suppl 1):S138-S142. PubMed, CrossRef
  9. Bär C, Blasco MA. Telomeres and telomerase as therapeutic targets to prevent and treat age-related diseases. F1000Res. 2016;5:F1000 Faculty Rev-89. PubMed, PubMedCentral, CrossRef
  10. Docherty MH, O’Sullivan ED, Bonventre JV, Ferenbach DA. Cellular Senescence in the Kidney. J Am Soc Nephrol. 2019;30(5):726-736. PubMed, PubMedCentral, CrossRef
  11. Shiels PG, McGuinness D, Eriksson M, Kooman JP, Stenvinkel P. The role of epigenetics in renal ageing. Nat Rev Nephrol. 2017;13(8):471-482. PubMed, CrossRef
  12. Brouilette S, Singh RK, Thompson JR, Goodall AH, Samani NJ. White cell telomere length and risk of premature myocardial infarction. Arterioscler Thromb Vasc Biol. 2003;23(5):842-846. PubMed, CrossRef
  13. Haycock PC, Heydon EE, Kaptoge S, Butterworth AS, Thompson A, Willeit P. Leucocyte telomere length and risk of cardiovascular disease: systematic review and meta-analysis. BMJ. 2014;349:g4227. PubMed, PubMedCentral, CrossRef
  14. Martin-Montalvo A, Mercken EM, Mitchell SJ, Palacios HH, Mote PL, Scheibye-Knudsen M, Gomes AP, Ward TM, Minor RK, Blouin MJ, Schwab M, Pollak M, Zhang Y, Yu Y, Becker KG, Bohr VA, Ingram DK, Sinclair DA, Wolf NS, Spindler SR, Bernier M, de Cabo R. Metformin improves healthspan and lifespan in mice. Nat Commun. 2013;4:2192. PubMed, PubMedCentral, CrossRef
  15. Xu M, Pirtskhalava T, Farr JN, Weigand BM, Palmer AK, Weivoda MM, Inman CL, Ogrodnik MB, Hachfeld CM, Fraser DG, Onken JL, Johnson KO, Verzosa GC, Langhi LGP, Weigl M, Giorgadze N, LeBrasseur NK, Miller JD, Jurk D, Singh RJ, Allison DB, Ejima K, Hubbard GB, Ikeno Y, Cubro H, Garovic VD, Hou X, Weroha SJ, Robbins PD, Niedernhofer LJ, Khosla S, Tchkonia T, Kirkland JL. Senolytics improve physical function and increase lifespan in old age. Nat Med. 2018;24(8):1246-1256. PubMed, PubMedCentral, CrossRef

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