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全基因组关联研究表明存在与腹部及内脏脂肪相关的性别特异性基因座。

Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.

作者信息

Sung Y J, Pérusse L, Sarzynski M A, Fornage M, Sidney S, Sternfeld B, Rice T, Terry J G, Jacobs D R, Katzmarzyk P, Curran J E, Jeffrey Carr J, Blangero J, Ghosh S, Després J-P, Rankinen T, Rao D C, Bouchard C

机构信息

Division of Biostatistics, Washington University School of Medicine, St Louis, MO, USA.

Department of Kinesiology, School of Medicine and Institute of Nutrition and Functional Foods, Laval University, Québec, Canada.

出版信息

Int J Obes (Lond). 2016 Apr;40(4):662-74. doi: 10.1038/ijo.2015.217. Epub 2015 Oct 20.

Abstract

BACKGROUND

To identify loci associated with abdominal fat and replicate prior findings, we performed genome-wide association (GWA) studies of abdominal fat traits: subcutaneous adipose tissue (SAT); visceral adipose tissue (VAT); total adipose tissue (TAT) and visceral to subcutaneous adipose tissue ratio (VSR).

SUBJECTS AND METHODS

Sex-combined and sex-stratified analyses were performed on each trait with (TRAIT-BMI) or without (TRAIT) adjustment for body mass index (BMI), and cohort-specific results were combined via a fixed effects meta-analysis. A total of 2513 subjects of European descent were available for the discovery phase. For replication, 2171 European Americans and 772 African Americans were available.

RESULTS

A total of 52 single-nucleotide polymorphisms (SNPs) encompassing 7 loci showed suggestive evidence of association (P<1.0 × 10(-6)) with abdominal fat in the sex-combined analyses. The strongest evidence was found on chromosome 7p14.3 between a SNP near BBS9 gene and VAT (rs12374818; P=1.10 × 10(-7)), an association that was replicated (P=0.02). For the BMI-adjusted trait, the strongest evidence of association was found between a SNP near CYCSP30 and VAT-BMI (rs10506943; P=2.42 × 10(-7)). Our sex-specific analyses identified one genome-wide significant (P<5.0 × 10(-8)) locus for SAT in women with 11 SNPs encompassing the MLLT10, DNAJC1 and EBLN1 genes on chromosome 10p12.31 (P=3.97 × 10(-8) to 1.13 × 10(-8)). The THNSL2 gene previously associated with VAT in women was also replicated (P=0.006). The six gene/loci showing the strongest evidence of association with VAT or VAT-BMI were interrogated for their functional links with obesity and inflammation using the Biograph knowledge-mining software. Genes showing the closest functional links with obesity and inflammation were ADCY8 and KCNK9, respectively.

CONCLUSIONS

Our results provide evidence for new loci influencing abdominal visceral (BBS9, ADCY8, KCNK9) and subcutaneous (MLLT10/DNAJC1/EBLN1) fat, and confirmed a locus (THNSL2) previously reported to be associated with abdominal fat in women.

摘要

背景

为了识别与腹部脂肪相关的基因座并重复先前的研究结果,我们对腹部脂肪特征进行了全基因组关联(GWA)研究:皮下脂肪组织(SAT);内脏脂肪组织(VAT);总脂肪组织(TAT)以及内脏与皮下脂肪组织比值(VSR)。

受试者与方法

对每个特征进行了合并性别和按性别分层的分析,分别对体重指数(BMI)进行(TRAIT-BMI)或不进行(TRAIT)调整,并通过固定效应荟萃分析合并特定队列的结果。共有2513名欧洲血统的受试者可用于发现阶段。用于重复验证的有2171名欧裔美国人和772名非裔美国人。

结果

在合并性别分析中,共有52个单核苷酸多态性(SNP)涵盖7个基因座显示出与腹部脂肪存在关联的提示性证据(P<1.0×10⁻⁶)。最强的证据发现于7号染色体p臂14.3区域,位于BBS9基因附近的一个SNP与内脏脂肪组织(VAT)之间(rs12374818;P=1.10×10⁻⁷),该关联得到了重复验证(P=0.02)。对于经BMI调整的特征,最强的关联证据发现于CYCSP30附近的一个SNP与内脏脂肪组织-体重指数(VAT-BMI)之间(rs10506943;P=2.42×10⁻⁷)。我们的性别特异性分析在女性中确定了一个全基因组显著(P<5.0×10⁻⁸)的皮下脂肪组织基因座,位于10号染色体p臂12.31区域,有11个SNP涵盖MLLT10、DNAJC1和EBLN1基因(P=3.97×10⁻⁸至1.13×10⁻⁸)。先前报道的与女性内脏脂肪组织相关的THNSL2基因也得到了重复验证(P=0.006)。使用Biograph知识挖掘软件对显示出与内脏脂肪组织或内脏脂肪组织-体重指数关联最强证据的6个基因/基因座,研究了它们与肥胖和炎症的功能联系。与肥胖和炎症显示出最密切功能联系的基因分别是ADCY8和KCNK9。

结论

我们的结果为影响腹部内脏(BBS9、ADCY8、KCNK9)和皮下(MLLT10/DNAJC1/EBLN1)脂肪的新基因座提供了证据,并证实了一个先前报道的与女性腹部脂肪相关的基因座(THNSL2)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9b8/4821694/9c21c0ead661/nihms729351f1.jpg

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