Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant.

Autor: Kandemir I; Department of Pediatrics, Istanbul Health and Technology University Faculty of Medicine, Istanbul, Turkey. dr.ibrahimkandemir@gmail.com., Sahin AY; Adolescent Health PhD Program, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Turkey., Oyaci Y; Istanbul Faculty of Medicine, Department of Medical Biology, Istanbul University, Istanbul, Turkey., Khudiyeva S; Department of Pediatrics, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey., Sahin M; Department of Gastroenterology, University of Health Sciences, Başakşehir Çam and Sakura City Hospital, Istanbul, Turkey., Aksakal MT; Adolescent Health PhD Program, Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Turkey., Pehlivan M; Department of Hematology, University of Health Sciences, Başakşehir Çam and Sakura City Hospital, Istanbul, Turkey., Bas F; Department of Pediatric Endocrinology, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey., Pehlivan S; Istanbul Faculty of Medicine, Department of Medical Biology, Istanbul University, Istanbul, Turkey.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2024 Oct 23; Vol. 14 (1), pp. 25055. Date of Electronic Publication: 2024 Oct 23.
DOI: 10.1038/s41598-024-77091-5
Abstrakt: It is known that telomere length (TL) (evaluated with T/S ratio) is shortened in the presence of obesity. In this study, we aimed to investigate how obesity in adolescents and non-alcoholic liver disease (NAFLD) within the obese group affect TL and the clinical significance of the human telomerase reverse transcriptase (hTERT) gene MNS16A VNTR variant in terms of NAFLD. Adolescents with exogenous obesity and healthy controls (aged 10-19 years) who applied to our adolescent outpatient clinic between May-October 2023 were included in this study. We performed upper abdominal ultrasonography to investigate the presence of NAFLD in adolescents with obesity and divided into two groups: those without hepatosteatosis (obese NAFLD (-)) and those with hepatosteatosis (obese NAFLD (+)). We recorded body weight, height, waist circumference, and blood pressure measurements and measured the T/S ratio (telomere sequence copy number/gene single copy number) by the Quantitative Polymerase Chain Reaction method. The groups were compared using frequentist and Bayesian methods. Eighty-three obese adolescents [63 NAFLD(+) 20 NAFLD(-)] and 69 lean controls were included in the study. Pairwise comparisons revealed that T/S ratio was significantly lower in the obese NAFLD (-) group than the obese NAFLD (+) and the control group (p = 0.025, p = 0.007, respectively). T/S ratio was lower in the LL allele group than in the other alleles (p = 0.022) and slightly higher in the obese group with metabolic syndrome compared to the obese group without metabolic syndrome (p = 0.072). hTERT-MNS16A-VNTR gene variant LL allele had a negative correlation with T/S ratio among the obese adolescent group. Patients with LL alleles had higher ALT, GGT, HOMA-IR, and ALT/AST. Diastolic blood pressure had a significant correlation with the T/S ratio. The T/S ratio was shorter in the obese adolescent group compared to healthy ones but was higher in the NAFLD (+) obese compared to the NAFLD (-) obese. ALT level and ALT/AST ratio were higher, T/S ratio was lower in the hTERT MNS16A VNTR variant LL allele group among obese adolescents. In addition, there was a significant correlation between the T/S ratio and diastolic blood pressure in obese adolescents.
(© 2024. The Author(s).)
Databáze: MEDLINE
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