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MODY patients exhibit shorter telomere length than non-diabetic subjects.

AbstractBACKGROUND:
Given the increasing evidence supporting the association between telomere shortening and diabetes, the aim of the present work was to establish whether MODY patients suffer a reduction in telomere lenght (TL) due to oxidative stress produced by chronic hyperglycemia, despite not presenting insulin resistance or inflammation.
METHODS:
We analysed clinical and biochemical parameters in 35 MODY2 and 12 MODY3 patients compared with 48 control subjects. The absolute telomere length (aTL) of peripheral blood leukocytes was measured using the quantitative polymerase chain reaction (qPCR).
RESULTS:
A significant negative correlation was observed between aTL and age in the whole population, among MODY patients and in each subtype studied, MODY2 and MODY3, which allowed us to validate the method. We found, for the first time, that MODY patients have shorter aTL with respect to non-diabetic controls (6.49 ± 3.31 kbp vs 11.13 ± 7.82 kbp, p = .006). However, no differences were found between MODY2 and MODY3. In addition, aTL showed a negative correlation with duration of the disease and fasting plasma glucose (FPG) levels in MODY patients in general and also with HbA1c in MODY2 patients in particular.
CONCLUSIONS:
Both MODY2 and MODY3 types present telomere shortening, which, at least partly, responds to HbA1c and FPG levels. These findings suggest comparable mechanisms underlying the attrition of TL. Taken together, our results on aTL in MODY patients may provide a parameter relatively easy and inexpensive to quantify in order to measure the impact of high glucose levels and potentially carry out antidiabetic treatment with stricter targets.
AuthorsAndrea L Millan, Sofía I Trobo, Alejandro de Dios, Martina Cerrato García, María S Pérez, Gloria E Cerrone, Gustavo D Frechtel, Ariel P López
JournalDiabetes/metabolism research and reviews (Diabetes Metab Res Rev) Vol. 37 Issue 2 Pg. e3374 (02 2021) ISSN: 1520-7560 [Electronic] England
PMID32588935 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2020 John Wiley & Sons Ltd.
Topics
  • Diabetes Mellitus, Type 2 (genetics)
  • Humans
  • Telomere (genetics)

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