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欧洲来源的肥胖相关基因座在非裔美国人中的意义。

Implication of European-derived adiposity loci in African Americans.

机构信息

Center for Diabetes Research, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

Int J Obes (Lond). 2012 Mar;36(3):465-73. doi: 10.1038/ijo.2011.131. Epub 2011 Jul 12.

Abstract

OBJECTIVE

Recent genome-wide association studies (GWAS) have identified multiple novel loci associated with adiposity in European-derived study populations. Limited study of these loci has been reported in African Americans. Here we examined the effects of these previously identified adiposity loci in African Americans.

METHODS

A total of 46 representative single-nucleotide polymorphisms (SNPs) in 19 loci that were previously reported in GWAS in Europeans (including FTO and MC4R) were genotyped in 4992 subjects from six African-American cohorts. These SNPs were tested for association with body mass index (BMI) after adjustment for age, gender, disease status and population structure in each cohort. Meta-analysis was conducted to combine the results.

RESULTS

Meta-analysis of 4992 subjects revealed seven SNPs near four loci, including NEGR1, TMEM18, SH2B1 /ATP2A1 and MC4R, showing significant association at 0.005<P<0.05, and had effect sizes between 0.04 and 0.06 s.d. units (or 0.30 to 0.44  g m(-2)) of BMI for each copy of the BMI-increasing allele. The most significantly associated SNPs (rs9424977, rs3101336 and rs2568958) are located in the NEGR1 gene (P=0.005, 0.020 and 0.019, respectively).

CONCLUSION

We replicated the association of variants at four loci in six African-American cohorts that demonstrated a consistent direction of association with previous studies of adiposity in Europeans. These loci are all highly expressed in the brain, consistent with an important role for central nervous system processes in weight regulation. However, further comprehensive examination of these regions may be necessary to fine map and elucidate for possible genetic differences between these two populations.

摘要

目的

最近的全基因组关联研究(GWAS)已经确定了多个与欧洲人群肥胖相关的新基因座。在非裔美国人中对这些基因座的研究有限。在这里,我们研究了这些先前确定的肥胖基因座在非裔美国人中的作用。

方法

在六个非裔美国人队列的 4992 名受试者中,对以前在欧洲人 GWAS 中报道的 19 个基因座的 46 个代表性单核苷酸多态性(SNP)进行了基因分型。在每个队列中,在调整年龄、性别、疾病状态和人口结构后,对这些 SNP 与体重指数(BMI)的关联进行了检验。进行了荟萃分析以合并结果。

结果

对 4992 名受试者的荟萃分析显示,四个基因座附近的七个 SNP,包括 NEGR1、TMEM18、SH2B1/ATP2A1 和 MC4R,在 0.005<P<0.05 时显示出显著相关性,并且每个 BMI 增加等位基因的 BMI 增加 0.04 至 0.06 个标准差(或 0.30 至 0.44 g m(-2)) 的效应大小。最显著相关的 SNP(rs9424977、rs3101336 和 rs2568958)位于 NEGR1 基因内(P=0.005、0.020 和 0.019)。

结论

我们在六个非裔美国人队列中复制了四个基因座的变异与欧洲人肥胖相关的关联,其关联方向与以前的研究一致。这些基因座在大脑中均高度表达,这与中枢神经系统在体重调节中的重要作用一致。然而,可能需要进一步全面检查这些区域,以精细定位和阐明这两个人群之间可能存在的遗传差异。

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