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瘦素与肥胖的遗传学:一项人类基因流行病学(HuGE)综述

Genetics of leptin and obesity: a HuGE review.

作者信息

Paracchini Valentina, Pedotti Paola, Taioli Emanuela

机构信息

Unit of Molecular and Genetic Epidemiology, Fondazione Policlinico IRCCS, Milan, Italy.

出版信息

Am J Epidemiol. 2005 Jul 15;162(2):101-14. doi: 10.1093/aje/kwi174. Epub 2005 Jun 22.

Abstract

Leptin is an important regulator of the mass of adipose tissue and of body weight; it operates by inhibiting food intake and stimulating energy expenditure. Some polymorphic genes involved in the regulation of leptin-the leptin gene (LEP A19G), the leptin receptor gene (LEPR Q223R, K109R, and K656N), and the peroxisome proliferator-activated receptor-gamma gene (PPARG P12A and C161T)--have been investigated as possible factors associated with obesity. Allelic frequencies of these polymorphisms show ethnic variation. The authors performed a meta-analysis of the available data on the association between these polymorphisms and obesity based on case-control studies. Odds ratios and 95% confidence intervals for obesity associated with leptin polymorphisms were calculated by using both fixed- and random-effects models. Results suggest no evidence of association between the genes under study and obesity. The lack of association could be due to the complex pathogenesis of obesity, which involves a number of genetic and environmental factors. Large studies including testing of multiple genes in both obese and lean subjects, with epidemiologic data on dietary habits in different ethnic groups, are necessary to better understand the role of leptin in regulating weight in human populations.

摘要

瘦素是脂肪组织质量和体重的重要调节因子;它通过抑制食物摄入和刺激能量消耗来发挥作用。一些参与瘦素调节的多态性基因——瘦素基因(LEP A19G)、瘦素受体基因(LEPR Q223R、K109R和K656N)以及过氧化物酶体增殖物激活受体γ基因(PPARG P12A和C161T)——已被作为与肥胖相关的可能因素进行研究。这些多态性的等位基因频率存在种族差异。作者基于病例对照研究对这些多态性与肥胖之间关联的现有数据进行了荟萃分析。通过使用固定效应模型和随机效应模型计算了与瘦素多态性相关的肥胖的比值比和95%置信区间。结果表明,所研究的基因与肥胖之间没有关联证据。缺乏关联可能是由于肥胖的发病机制复杂,涉及多种遗传和环境因素。需要开展大型研究,包括对肥胖和瘦人受试者进行多个基因检测,并获取不同种族饮食习惯的流行病学数据,以便更好地了解瘦素在调节人群体重中的作用。

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