Insulin Resistance Risk in Normal BMI Individuals: Investigating the Role of Genetic Polymorphisms in RNF138, ABCA1, and ESRRG-GPATCH2 Genes - A Case-Control Study in the Indian Population

Sabitha Thummala, Sarah Fathima, Nithya Kruthi, Junaid Ahmed Khan Ghori, Katherine Saikia, Balamurali AR, Rahul Ranganathan
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Abstract

Abstract Background: India, characterised as the "diabetes capital" of the world, faces a rapidly increasing diabetes crisis with over 65 million cases diagnosed. Despite the growing prevalence, the genetic underpinnings of insulin resistance (IR) among Indians with normal BMI remain understudied. This research aims to fill the knowledge gap by investigating the association of specific gene variants (RNF138, ABCA1, and ESRRG-GPATCH2) with IR risk in this demographic. Methods: A total of 191 participants (90 men, 101 women) were recruited for this cross-sectional study. Participants were categorized into cases (HOMA2-IR > 2) and controls (HOMA2-IR < 2) based on Homeostasis Model Assessment Insulin Resistance values. Genotyping for rs4799327 (RNF138), rs2275543 (ABCA1), and rs1497828 (ESRRG-GPATCH2) was performed using the Illumina Infinium Global Screening Array. Statistical analyses, including odds ratios (ORs), 95% confidence intervals (CIs), and inheritance model analysis, were conducted to assess the association between genotypes and IR. Results: Significant associations were found between IR and genetic variants rs4799327 in RNF138 and rs1497828 in ESRRG-GPATCH2 (dominant inheritance model) and rs2275543 in ABCA1 (additive model). The study highlights a notable susceptibility to IR linked to these genetic markers among normal BMI individuals in the Indian population. Conclusions:This study underscores the importance of genetic factors in the risk of developing insulin resistance among Indians with normal BMI, suggesting a complex interplay of genetics beyond traditional risk factors. These findings necessitate further research into the functional significance of these associations and their potential implications for targeted interventions and preventive strategies in high-risk populations.
正常体重指数个体的胰岛素抵抗风险:调查 RNF138、ABCA1 和 ESRRG-GPATCH2 基因多态性的作用--印度人群病例对照研究
摘要 背景:印度被誉为世界 "糖尿病之都",面临着迅速增长的糖尿病危机,确诊病例超过 6500 万。尽管患病率不断上升,但对体重指数正常的印度人胰岛素抵抗(IR)的遗传基础研究仍然不足。本研究旨在通过调查特定基因变异(RNF138、ABCA1 和 ESRRG-GPATCH2)与该人群胰岛素抵抗风险的关联,填补这一知识空白。研究方法这项横断面研究共招募了 191 名参与者(90 名男性,101 名女性)。根据胰岛素抵抗稳态模型评估值将参与者分为病例(HOMA2-IR >2)和对照组(HOMA2-IR <2)。使用 Illumina Infinium 全球筛查阵列对 rs4799327(RNF138)、rs2275543(ABCA1)和 rs1497828(ESRRG-GPATCH2)进行了基因分型。为评估基因型与 IR 之间的关联,进行了统计分析,包括几率比(OR)、95% 置信区间(CI)和遗传模型分析。结果发现发现 IR 与 RNF138 基因变异 rs4799327 和 ESRRG-GPATCH2 基因变异 rs1497828(显性遗传模型)以及 ABCA1 基因变异 rs2275543(加性遗传模型)之间存在显著关联。该研究强调,在印度人群中,正常体重指数个体对红外的易感性与这些遗传标记有关。结论:这项研究强调了遗传因素在体重指数正常的印度人胰岛素抵抗风险中的重要性,表明除了传统的风险因素外,遗传因素还存在复杂的相互作用。因此,有必要进一步研究这些关联的功能意义及其对高危人群的针对性干预和预防策略的潜在影响。
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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