Delving Into the Interaction Between Exercise and Diabetes on Methylation of the FKBP5 Gene.

IF 3.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Journal of Diabetes Research Pub Date : 2025-02-19 eCollection Date: 2025-01-01 DOI:10.1155/jdr/1162708
Teng-Chi Yang, Jen Pi Tsai, Honda Hsu, Yen-Chung Chen, Yi-Chia Liaw, Shu Yi Hsu, Hao Jan Yang, Yung-Po Liaw
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引用次数: 0

Abstract

Objective: FKBP5 is a critical gene involved in regulating the hypothalamic-pituitary-adrenal (HPA) axis and stress response. Aberrant DNA methylation at FKBP5 cytosine-phosphate-guanine (CpG) sites, such as cg22363520 and cg00862770, has been implicated in mental health disorders and metabolic diseases, including Type 2 diabetes. Exercise is a modulator of DNA methylation and metabolic health. This study investigates the interaction between exercise, diabetes, and FKBP5 methylation at cg22363520 and cg00862770 and explores their implications for mental health and disease development. Materials and Methods: FKBP5 methylation levels at cg22363520 and cg00862770 were analyzed in a cohort stratified by diabetes and exercise. Multiple linear regression models assessed the main effects and interactions of exercise and diabetes on FKBP5 methylation, with further stratified analyses for site-specific effects. Results: Exercise and diabetes showed significant and site-specific effects on FKBP5 methylation at cg22363520 and cg00862770. At cg22363520, exercise significantly reduced methylation levels in nondiabetic participants (β = -0.00195, p = 0.0157), while no significant effect was observed in diabetic individuals. Conversely, at cg00862770, exercise significantly decreased methylation levels in diabetic participants (β = -0.00611, p = 0.0081), with no significant effect in the nondiabetic group. Diabetes itself was associated with increased FKBP5 methylation at both sites, particularly in individuals without regular exercise. Additionally, significant interaction effects between exercise and diabetes were identified for both cg22363520 (p = 0.0336) and cg00862770 (p = 0.0021), highlighting the interplay between metabolic status and physical activity in regulating FKBP5 methylation. Conclusion: This study demonstrates that the effects of exercise on FKBP5 methylation are site-specific and influenced by diabetes status. Exercise reduces methylation at cg22363520 in nondiabetics and at cg00862770 in diabetics, indicating its role in modulating epigenetic regulation of stress and metabolic pathways. These findings underscore the interplay between exercise, diabetes, and FKBP5 methylation, with potential implications for improving mental health and metabolic outcomes.

运动与糖尿病对FKBP5基因甲基化的相互作用研究
目的:FKBP5是参与调节下丘脑-垂体-肾上腺(HPA)轴和应激反应的关键基因。FKBP5胞嘧啶-磷酸-鸟嘌呤(CpG)位点(如cg22363520和cg00862770)的异常DNA甲基化与精神健康障碍和代谢性疾病(包括2型糖尿病)有关。运动是DNA甲基化和代谢健康的调节剂。本研究探讨了运动、糖尿病和FKBP5基因cg22363520和cg00862770甲基化之间的相互作用,并探讨了它们对心理健康和疾病发展的影响。材料和方法:在糖尿病和运动分层的队列中分析FKBP5位点cg22363520和cg00862770的甲基化水平。多元线性回归模型评估了运动和糖尿病对FKBP5甲基化的主要影响和相互作用,并对特定部位的影响进行了进一步的分层分析。结果:运动和糖尿病对FKBP5位点cg22363520和cg00862770的甲基化有显著的位点特异性影响。在cg22363520,运动显著降低了非糖尿病参与者的甲基化水平(β = -0.00195, p = 0.0157),而在糖尿病个体中没有观察到显著的影响。相反,在cg00862770时,运动显著降低了糖尿病参与者的甲基化水平(β = -0.00611, p = 0.0081),而在非糖尿病组中没有显著影响。糖尿病本身与这两个位点的FKBP5甲基化增加有关,特别是在没有定期运动的个体中。此外,cg22363520 (p = 0.0336)和cg00862770 (p = 0.0021)在运动和糖尿病之间存在显著的相互作用,强调了代谢状态和身体活动在调节FKBP5甲基化中的相互作用。结论:本研究表明,运动对FKBP5甲基化的影响具有位点特异性,并受糖尿病状态的影响。运动降低非糖尿病患者cg22363520位点甲基化和糖尿病患者cg00862770位点甲基化,表明其在调节应激和代谢途径的表观遗传调控中发挥作用。这些发现强调了运动、糖尿病和FKBP5甲基化之间的相互作用,对改善心理健康和代谢结果有潜在的影响。
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来源期刊
Journal of Diabetes Research
Journal of Diabetes Research ENDOCRINOLOGY & METABOLISM-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
8.40
自引率
2.30%
发文量
152
审稿时长
14 weeks
期刊介绍: Journal of Diabetes Research is a peer-reviewed, Open Access journal that publishes research articles, review articles, and clinical studies related to type 1 and type 2 diabetes. The journal welcomes submissions focusing on the epidemiology, etiology, pathogenesis, management, and prevention of diabetes, as well as associated complications, such as diabetic retinopathy, neuropathy and nephropathy.
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