Department of Medicine, Coordination Centre for Clinical Trials, University of Leipzig, Leipzig, Germany.
Eur J Hum Genet. 2010 Jan;18(1):104-10. doi: 10.1038/ejhg.2009.107.
The association between common variants in the FTO gene with weight, adiposity and body mass index (BMI) has now been widely replicated. Although the causal variant has yet to be identified, it most likely maps within a 47 kb region of intron 1 of FTO. We performed a genome-wide association study in the Sorbian population and evaluated the relationships between FTO variants and BMI and fat mass in this isolate of Slavonic origin resident in Germany. In a sample of 948 Sorbs, we could replicate the earlier reported associations of intron 1 SNPs with BMI (eg, P-value=0.003, beta=0.02 for rs8050136). However, using genome-wide association data, we also detected a second independent signal mapping to a region in intron 2/3 about 40-60 kb away from the originally reported SNPs (eg, for rs17818902 association with BMI P-value=0.0006, beta=-0.03 and with fat mass P-value=0.0018, beta=-0.079). Both signals remain independently associated in the conditioned analyses. In conclusion, we extend the evidence that FTO variants are associated with BMI by putatively identifying a second susceptibility allele independent of that described earlier. Although further statistical analysis of these findings is hampered by the finite size of the Sorbian isolate, these findings should encourage other groups to seek alternative susceptibility variants within FTO (and other established susceptibility loci) using the opportunities afforded by analyses in populations with divergent mutational and/or demographic histories.
FTO 基因中的常见变异与体重、肥胖和体重指数 (BMI) 的关联已被广泛复制。尽管尚未确定因果变异,但它很可能位于 FTO 内含子 1 的 47 kb 区域内。我们在索布人群中进行了全基因组关联研究,并评估了 FTO 变异与 BMI 和脂肪量之间的关系,这些变异在居住在德国的这个斯拉夫起源的隔离人群中。在 948 名索布人的样本中,我们可以复制先前报道的内含子 1 SNP 与 BMI 之间的关联(例如,rs8050136 的 P 值=0.003,β=0.02)。然而,使用全基因组关联数据,我们还检测到第二个独立的信号,该信号映射到距离最初报道的 SNP 约 40-60 kb 的内含子 2/3 区域(例如,rs17818902 与 BMI 的关联 P 值=0.0006,β=-0.03,与脂肪量的关联 P 值=0.0018,β=-0.079)。在条件分析中,这两个信号仍然独立相关。总之,我们通过假定鉴定出与先前描述的 SNP 无关的第二个易感等位基因,扩展了 FTO 变异与 BMI 相关的证据。尽管由于索布人的隔离规模有限,对这些发现的进一步统计分析受到阻碍,但这些发现应该鼓励其他群体利用在具有不同突变和/或人口历史的人群中进行分析的机会,在 FTO(和其他已建立的易感基因座)中寻找替代的易感变异。