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Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups

机译:在法国和德国研究小组针对早期发作的极端肥胖的基因组全关联研究的联合分析中确定了两个新的体重调节基因座

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摘要

Meta-analyses of population-based genome-wide association studies (GWAS) in adults have recently led to the detection of new genetic loci for obesity. Here we aimed to discover additional obesity loci in extremely obese children and adolescents. We also investigated if these results generalize by estimating the effects of these obesity loci in adults and in population-based samples including both children and adults. We jointly analysed two GWAS of 2,258 individuals and followed-up the best, according to lowest p-values, 44 single nucleotide polymorphisms (SNP) from 21 genomic regions in 3,141 individuals. After this DISCOVERY step, we explored if the findings derived from the extremely obese children and adolescents (10 SNPs from 5 genomic regions) generalized to (i) the population level and (ii) to adults by genotyping another 31,182 individuals (GENERALIZATION step). Apart from previously identified FTO, MC4R, and TMEM18, we detected two new loci for obesity: one in SDCCAG8 (serologically defined colon cancer antigen 8 gene; p = 1.85×10−8 in the DISCOVERY step) and one between TNKS (tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase gene) and MSRA (methionine sulfoxide reductase A gene; p = 4.84×10−7), the latter finding being limited to children and adolescents as demonstrated in the GENERALIZATION step. The odds ratios for early-onset obesity were estimated at ∼1.10 per risk allele for both loci. Interestingly, the TNKS/MSRA locus has recently been found to be associated with adult waist circumference. In summary, we have completed a meta-analysis of two GWAS which both focus on extremely obese children and adolescents and replicated our findings in a large followed-up data set. We observed that genetic variants in or near FTO, MC4R, TMEM18, SDCCAG8, and TNKS/MSRA were robustly associated with early-onset obesity. We conclude that the currently known major common variants related to obesity overlap to a substantial degree between children and adults.
机译:对成年人的基于人群的全基因组关联研究(GWAS)的荟萃分析最近导致了肥胖症新基因位点的检测。在这里,我们旨在发现极度肥胖的儿童和青少年中的其他肥胖基因座。我们还通过估计这些肥胖基因座对成年人以及包括儿童和成年人在内的人群样本中的影响,来研究这些结果是否普遍。我们联合分析了2258名个体的两个GWAS,并根据p值最低的结果进行了最佳随访,该值来自3141名个体的21个基因组区域的44个单核苷酸多态性(SNP)。在这一发现步骤之后,我们探索了来自极度肥胖的儿童和青少年(来自5个基因组区域的10个SNP)得出的发现是否通过对另外31,182个个体进行基因分型而推广到(i)人群水平和(ii)成人(GENERALIZATION步骤)。除了先前确定的FTO,MC4R和TMEM18,我们还发现了两个肥胖的新基因座:一个在SDCCAG8中(血清学定义的结肠癌抗原8基因;在DISCOVERY步骤中p = 1.85×10 -8 ) TNKS(tankyrase,与TRF1相互作用的锚蛋白相关的ADP-核糖聚合酶基因)和MSRA(甲硫氨酸亚砜还原酶A基因; p = 4.84×10 −7 )之间存在一个,后者仅限于概括步骤中显示的儿童和青少年。估计这两个基因座的早发性肥胖的比值比为每个风险等位基因约1.10。有趣的是,最近发现TNKS / MSRA位点与成人腰围有关。总而言之,我们已经完成了对两个GWAS的荟萃分析,这两个GWAS都针对极度肥胖的儿童和青少年,并在大量的后续数据集中复制了我们的发现。我们观察到FTO,MC4R,TMEM18,SDCCAG8和TNKS / MSRA中或附近的遗传变异与早期肥胖症密切相关。我们得出结论,目前已知的与肥胖有关的主要常见变异在儿童和成人之间有很大程度的重叠。

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