Suppr超能文献

ACDC/脂联素基因多态性与儿童期和成人期严重肥胖有关。

ACDC/adiponectin polymorphisms are associated with severe childhood and adult obesity.

作者信息

Bouatia-Naji Nabila, Meyre David, Lobbens Stéphane, Séron Karin, Fumeron Frédéric, Balkau Beverley, Heude Barbara, Jouret Béatrice, Scherer Philipp E, Dina Christian, Weill Jacques, Froguel Philippe

机构信息

Centre National de la Recherche Scientifique UMR8090, Pasteur Institute of Lille, France.

出版信息

Diabetes. 2006 Feb;55(2):545-50. doi: 10.2337/diabetes.55.02.06.db05-0971.

Abstract

Common single nucleotide polymorphisms (SNPs) in the ACDC adiponectin encoding gene have been associated with insulin resistance and type 2 diabetes in several populations. Here, we investigate the role of SNPs -11,377C > G, -11,391G > A, +45T > G, and +276G > T in 2,579 French Caucasians (1,229 morbidly obese and 1,350 control subjects). We found an association between severe forms of obesity and -11,377C (odds ratio 1.23, P = 0.001) and +276T (1.19, P = 0.006). Surprisingly, alternative alleles -11,377G and +276G have been previously reported as risk factors for type 2 diabetes. Transmission disequilibrium tests showed a trend in overtransmission (56.7%) of a risk haplotype 1((C))-1((G))-1((T))-2((T)) including -11,377C and +276T in 634 obesity trios (P = 0.097). Family-based analysis in 400 trios from the general population indicated association between obesity haplotype and higher adiponectin levels, suggesting a role of hyperadiponectinemia in weight gain. However, experiments studying the putative roles of SNPs -11,377C > G and +276G > T on ACDC functionality were not conclusive. In contrast, promoter SNP -11,391G > A was associated with higher adiponectin levels in obese children (P = 0.005) and in children from the general population (0.00007). In vitro transcriptional assays showed that -11,391A may increase ACDC activity. In summary, our study suggests that variations at the ACDC/adiponectin gene are associated with risk of severe forms of obesity. However, the mechanisms underlying these possible associations are not fully understood.

摘要

脂联素编码基因ACDC中的常见单核苷酸多态性(SNP)在多个人群中与胰岛素抵抗及2型糖尿病相关。在此,我们在2579名法国白种人(1229名病态肥胖者和1350名对照者)中研究了SNP -11377C>G、-11391G>A、+45T>G和+276G>T的作用。我们发现严重肥胖形式与-11377C(优势比1.23,P = 0.001)和+276T(1.19,P = 0.006)之间存在关联。令人惊讶的是,先前已报道替代等位基因-11377G和+276G是2型糖尿病的风险因素。传递不平衡检验显示,在634个肥胖三联体中,包含-11377C和+276T的风险单倍型1((C))-1((G))-1((T))-2((T))存在过度传递趋势(56.7%)(P = 0.097)。在来自普通人群的400个三联体中进行的基于家系的分析表明,肥胖单倍型与较高的脂联素水平相关,提示高脂联素血症在体重增加中起作用。然而,研究SNP -11377C>G和+276G>T对ACDC功能假定作用的实验尚无定论。相比之下,启动子SNP -11391G>A与肥胖儿童(P = 0.005)及普通人群儿童(0.00007)中较高的脂联素水平相关。体外转录分析表明,-11391A可能会增加ACDC活性。总之,我们的研究提示,ACDC/脂联素基因的变异与严重肥胖形式的风险相关。然而,这些可能关联背后的机制尚未完全明了。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验