Study of DNA Methylation in Offsprings of Individuals with Type 2 Diabetes Mellitus

Sukhraj Kaur, R. Kapahi, I. Grover, Ritu Sharma, P. Sandhu
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Abstract

Introduction:  Epigenetic is study of changes in gene expression that occur by changing the DNA methylation and remodeling chromatin. It may also be affected by the environment. It is an important pathogenic mechanisms in complex multifactorial diseases such as type two diabetes. Recent genome-wide association studies have identified a number of genetic variants that explain some of the inter individual variation in diabetes susceptibility. Thus keeping in view, the role of epigenetic mechanisms particularly DNA methylation, the present study was conducted to find out DNA methylation (Whole DNA) in offsprings of individuals with type 2 Diabetes Mellitus. Methods: For the present study, the families of one hundred Diabetic individuals were enrolled. All the off springs of diabetics above the age of 18 years were recruited for the present study. All the samples collected were analyzed for Fasting plasma glucose, Glycosylated Hemoglobin, Lipid profile complete and DNA methylation (5mcytosine). Results: The study included 100 diabetic individuals and their off springs in the age range of 18-35 years. DNA methylation measured as 5mc% was significantly (p<0.001) more in IFG and Diabetic offsprings as compared to normal individuals both males and females. Conclusions: Altered DNA Methylation in individuals of the age group 18-24 years indicates towards deranged metabolism in these individuals, leading to impaired fasting glucose and making them more prone to type 2 Diabetes Mellitus and its complications at a later age.
2 型糖尿病患者后代 DNA 甲基化研究
简介 表观遗传学研究通过改变 DNA 甲基化和重塑染色质来改变基因表达。它也可能受到环境的影响。在复杂的多因素疾病(如二型糖尿病)中,表观遗传是一种重要的致病机制。最近的全基因组关联研究发现了一些基因变异,它们可以解释糖尿病易感性的一些个体间差异。因此,考虑到表观遗传机制,特别是 DNA 甲基化的作用,本研究旨在了解 2 型糖尿病患者后代的 DNA 甲基化(全 DNA)情况。研究方法在本研究中,100 个糖尿病患者的家庭被纳入研究范围。本研究招募了所有 18 岁以上糖尿病患者的后代。收集的所有样本都进行了空腹血浆葡萄糖、糖化血红蛋白、血脂全谱和 DNA 甲基化(5mcytosine)分析。结果研究对象包括 100 名年龄在 18-35 岁之间的糖尿病患者及其后代。与正常人(男性和女性)相比,IFG 和糖尿病后代的 DNA 甲基化(5mc%)显著增加(p<0.001)。结论18-24 岁年龄组的 DNA 甲基化改变表明这些人的新陈代谢失调,导致空腹血糖受损,使他们更容易在晚年患上 2 型糖尿病及其并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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