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首页> 外文期刊>Human Genetics >Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study.
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Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study.

机译:西班牙裔家庭脂联素和肥胖症的遗传分析:IRAS家庭研究。

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Adiponectin, coded for by the APM1 gene, is a novel adipocyte-derived hormone implicated in energy homeostasis and obesity. Several genetic studies have observed evidence of association between APM1 gene polymorphisms and features of the metabolic syndrome, such as insulin resistance and obesity. As part of a comprehensive genetic analysis of the APM1 gene, we have screened 96 unrelated individuals for polymorphisms in the promoter, coding regions, and 3'untranslated region (UTR). Three promoter single-nucleotide polymorphisms (SNPs), two rare coding SNPs (G113A and T1233C), and 13 SNPs in the 3'UTR were identified. Eighteen SNPs were genotyped in 811 Hispanic individuals from 45 families in the IRAS Family Study (IRASFS). SNPs were tested for association with six obesity quantitative traits (body mass index, waist, waist:hip ratio, subcutaneous adipose tissue, visceral adipose tissue, and visceral:subcutaneous ratio). Significant evidence of association to at least one of the obesity traits was identified in seven of the 18 SNPs (<0.001-0.05). The promoter SNP INS CA-11156 was the most consistently associated SNP and was associated significantly with all measures of obesity, except the visceral:subcutaneous ratio (P-values 0.009-0.03). Haplotype analysis supported this evidence of association, with haplotypes containing an insertion of one CA repeat at position -11156 consistently being associated with lower obesity values (P-value <0.001-0.05). The adiponectin polymorphisms, in particular those in the promoter region, thus show significant association with obesity measures in the Hispanic population. Additional studies are needed to confirm our findings and determine which polymorphism causes the functional effect.
机译:脂联素由APM1基因编码,是一种新的脂肪细胞源性激素,与能量稳态和肥胖有关。几项遗传研究已经观察到APM1基因多态性与代谢综合征特征(如胰岛素抵抗和肥胖症)之间存在关联的证据。作为APM1基因全面遗传分析的一部分,我们已经筛选了96个无关个体的启动子,编码区和3'非翻译区(UTR)多态性。在3'UTR中鉴定出三个启动子单核苷酸多态性(SNP),两个罕见编码SNP(G113A和T1233C)和13个SNP。在IRAS家庭研究(IRASFS)中,在来自45个家庭的811名西班牙裔个体中对18个SNP进行了基因分型。测试了SNP与六个肥胖症定量特征(体重指数,腰围,腰围:臀围比率,皮下脂肪组织,内脏脂肪组织和内脏皮下比率)的关联。在18个SNP中的7个中,发现了与至少一种肥胖性状相关的重要证据(<0.001-0.05)。启动子SNP INS CA-11156是最一致的SNP,并且与所有肥胖测量指标都显着相关,除了内脏:皮下比例(P值0.009-0.03)。单倍型分析支持这种关联的证据,单倍型包含在-11156位置插入一个CA重复序列,始终与较低的肥胖值相关(P值<0.001-0.05)。脂联素多态性,特别是在启动子区域的多态性,与西班牙裔人群的肥胖症测量结果具有显着相关性。需要进一步的研究来证实我们的发现并确定哪种多态性会导致功能影响。

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