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瘦素中的基因变异:印度南部人群肥胖和瘦素水平的决定因素

Genetic variants in leptin: Determinants of obesity and leptin levels in South Indian population.

作者信息

Dasgupta Shruti, Salman Mohammed, Siddalingaiah Lokesh B, Lakshmi G L, Xaviour D, Sreenath Jwalapuram

机构信息

Department of Studies in Biotechnology; University of Mysore ; Mysore, Karnataka, India.

Department of Studies in Biochemistry; University of Mysore ; Mysore, Karnataka, India ; Anthropological Survey of India, Southern Regional Center ; Mysore, Karnataka, India.

出版信息

Adipocyte. 2014 Dec 20;4(2):135-40. doi: 10.4161/21623945.2014.975538. eCollection 2015 Apr-Jun.

Abstract

The revelation of leptin action mechanisms has led to various attempts to establish the association of polymorphisms in the leptin gene with obesity-related phenotypes. But, outcomes have been contradicting, which made the information on the role of the leptin gene in regulating the mechanism of pathophysiology of obesity inexplicable. Moreover, none of the studies are known to have similar implications on the Indian population. To address such contradictions, our study aims to evaluate the association of leptin gene polymorphism with obesity and leptin levels in a South Indian Population. A total of 304 cases (BMI≥27.5) and 309 controls (BMI≤23) from local inhabitants of Mysore, Karnataka were recruited for the study. The leptin gene variants rs7799039, rs2167270 and rs4731426 independently, as well as in 4 haplotype combinations, were found to be significantly associated with the risk of obesity. An increasing trend in BMI and leptin levels was observed with every addition of A and C minor alleles of exonic variant (rs2167270) and intronic variant (rs4731426) respectively. However, only AA genotype of SNP rs7799039 was positively associated with BMI. None of the SNPs were associated with fat percentage and waist to hip ratio. On a whole, this data suggests that the common polymorphisms in the leptin gene are strong predictors of obesity and leptin levels in South Indians.

摘要

瘦素作用机制的揭示引发了各种尝试,以确定瘦素基因多态性与肥胖相关表型之间的关联。但是,结果相互矛盾,这使得关于瘦素基因在调节肥胖病理生理机制中作用的信息难以解释。此外,尚无研究表明对印度人群有类似影响。为了解决这些矛盾,我们的研究旨在评估南印度人群中瘦素基因多态性与肥胖及瘦素水平之间的关联。本研究招募了来自卡纳塔克邦迈索尔当地居民的304例病例(BMI≥27.5)和309例对照(BMI≤23)。发现瘦素基因变体rs7799039、rs2167270和rs4731426单独以及4种单倍型组合均与肥胖风险显著相关。分别观察到外显子变体(rs2167270)和内含子变体(rs4731426)的A和C次要等位基因每增加一个,BMI和瘦素水平就有上升趋势。然而,只有SNP rs7799039的AA基因型与BMI呈正相关。这些单核苷酸多态性均与脂肪百分比和腰臀比无关。总体而言,这些数据表明瘦素基因中的常见多态性是南印度人肥胖和瘦素水平的有力预测指标。

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