CNRS-UMR8199-Institute of Biology, Pasteur Institute, Lille, France.
Obesity (Silver Spring). 2011 Apr;19(4):833-9. doi: 10.1038/oby.2010.226. Epub 2010 Oct 21.
A recent study suggested that four CD36 polymorphisms (namely rs3211867, rs3211883, rs3211908, and rs1527483) were associated with an increased risk of obesity, an increased BMI and percentage of body fat in European adolescents. We first attempted to confirm these results in three independent case-control genome-wide association studies (GWAS) data totaling 3,509 subjects of French and German origin, but we were unable to find any association of these variants with early onset obesity risk. We then genotyped the four CD36 single-nucleotide polymorphisms (SNPs) in a large population-based study of 4,667 Finnish subjects and we did not replicate any of the recently reported associations with BMI. By combining all available data in a meta-analysis (N = 9,973), we found no evidence for an association of the reported four variants in CD36 with increased obesity risk or increased BMI (0.07 ≤ P values ≤ 0.93). Finally, we assessed the contribution of the full CD36 locus gene variation to obesity risk in 3,509 subjects and we did not detect any significant association with obesity after correction for multiple testing. In summary, we were unable to confirm the recently reported association of variants in CD36 with early onset obesity in populations of European ancestry.
最近的一项研究表明,四个 CD36 多态性(即 rs3211867、rs3211883、rs3211908 和 rs1527483)与肥胖风险增加、欧洲青少年 BMI 和体脂百分比增加有关。我们首先试图在三个独立的病例对照全基因组关联研究(GWAS)数据中验证这些结果,这些数据共包含 3509 名法裔和德裔受试者,但我们未能发现这些变体与早期肥胖风险之间存在任何关联。然后,我们对 4667 名芬兰受试者进行了基于人群的大型研究,对这四个 CD36 单核苷酸多态性(SNP)进行了基因分型,我们没有复制与 BMI 相关的任何最近报道的关联。通过对所有可用数据进行荟萃分析(N=9973),我们没有发现报告的 CD36 中的四个变体与肥胖风险增加或 BMI 增加(0.07≤P 值≤0.93)相关的证据。最后,我们评估了完整的 CD36 基因变异在 3509 名受试者中的肥胖风险中的作用,并且在经过多次测试校正后,我们没有发现任何与肥胖相关的显著关联。总之,我们无法证实最近报道的 CD36 变体与欧洲血统人群中早期肥胖的关联。