Talbert Matthew E, Langefeld Carl D, Ziegler Julie T, Haffner Steven M, Norris Jill M, Bowden Donald W
Program in Molecular Medicine and Translational Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Obesity (Silver Spring). 2009 Aug;17(8):1554-62. doi: 10.1038/oby.2009.94. Epub 2009 Apr 9.
The genome-wide association study by Herbert et al. identified the INSIG2 single-nucleotide polymorphism (SNP) rs7566605 as contributing to increased BMI in ethnically distinct cohorts. The present study sought to further clarify the matter, by testing whether SNPs of INSIG2 influenced quantitative adiposity or glucose homeostasis traits in Hispanics of the Insulin Resistance Atherosclerosis Family Study (IRASFS). Using a tagging SNP approach, rs7566605 and 31 additional SNPs were genotyped in 1,425 IRASFS Hispanics. SNPs were tested for association with six adiposity measures: BMI, waist circumference (WAIST), waist-to-hip ratio (WHR), subcutaneous adipose tissue (SAT), visceral adipose tissue (VAT), and VAT to SAT ratio (VSR). SNPs were also tested for association with fasting glucose (GFAST), fasting insulin (FINS), and three measures obtained from the frequently sampled intravenous glucose tolerance test: insulin sensitivity (S(I)), acute insulin response (AIR), and disposition index (DI). Most prominent association was observed with direct computed tomography (CT)-measured adiposity phenotypes, including VAT, SAT, and VSR (P values range from 0.007 to 0.044 for rs17586756, rs17047718, rs17047731, rs9308762, rs12623648, and rs11673900). Multiple SNP associations were observed with all glucose homeostasis traits (P values range from 0.001 to 0.031 for rs17047718, rs17047731, rs2161829, rs10490625, rs889904, and rs12623648). Using BMI as a covariate in evaluation of glucose homeostasis traits slightly reduced their association. However, association with adiposity and glucose homeostasis phenotypes is not significant following multiple comparisons adjustment. Trending association after multiple comparisons adjustment remains suggestive of a role for genetic variation of INSIG2 in obesity, but these results require validation.
赫伯特等人开展的全基因组关联研究确定,INSIG2单核苷酸多态性(SNP)rs7566605在不同种族队列中导致体重指数(BMI)升高。本研究旨在通过检测INSIG2的SNP是否影响胰岛素抵抗动脉粥样硬化家族研究(IRASFS)中西班牙裔人群的定量肥胖或葡萄糖稳态特征,进一步阐明这一问题。采用标签SNP方法,对1425名IRASFS西班牙裔人群的rs7566605及另外31个SNP进行基因分型。检测这些SNP与六种肥胖指标的关联:BMI、腰围(WAIST)、腰臀比(WHR)、皮下脂肪组织(SAT)、内脏脂肪组织(VAT)以及VAT与SAT比值(VSR)。还检测这些SNP与空腹血糖(GFAST)、空腹胰岛素(FINS)以及从频繁采样静脉葡萄糖耐量试验获得的三个指标的关联:胰岛素敏感性(S(I))、急性胰岛素反应(AIR)和处置指数(DI)。观察到与直接计算机断层扫描(CT)测量的肥胖表型存在最显著的关联,包括VAT、SAT和VSR(rs17586756、rs17047718、rs17047731、rs9308762、rs12623648和rs11673900的P值范围为0.007至0.044)。观察到所有葡萄糖稳态特征均存在多个SNP关联(rs17047718、rs17047731、rs2161829、rs10490625、rs889904和rs12623648的P值范围为0.001至0.031)。在评估葡萄糖稳态特征时将BMI作为协变量使用,略微降低了它们之间的关联。然而,在进行多重比较校正后,与肥胖和葡萄糖稳态表型的关联并不显著。多重比较校正后的趋势性关联仍提示INSIG2基因变异在肥胖中发挥作用,但这些结果需要验证。