Song Yiqing, You Nai-Chieh, Hsu Yi-Hsiang, Howard Barbara V, Langer Robert D, Manson Joann E, Nathan Lauren, Niu Tianhua, F Tinker Lesley, Liu Simin
Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Obesity (Silver Spring). 2008 Nov;16(11):2472-80. doi: 10.1038/oby.2008.408. Epub 2008 Sep 11.
The FTO gene was recently identified as a susceptibility locus for both obesity and type 2 diabetes by whole-genome association analyses of several European populations. We tested for an association between FTO risk alleles and obesity and diabetes in a well-characterized multiethnic cohort of postmenopausal women in the United States. We genotyped two most significantly associated single-nucleotide polymorphisms (SNPs) (rs9939609 and rs8050136) in intron 1 of FTO gene in a nested case-control study of 1,517 diabetes cases and 2,123 controls from the Women's Health Initiative-Observational Study (WHI-OS). The allelic frequencies of either rs9939609 or rs8050136 differed widely across four ethnic groups. The frequency of the rare allele A of rs9939609 among controls was much lower in Asians/Pacific Islanders (17%) than in blacks (45%), whites (40%), and Hispanics (31%). We found significant associations of rs9939609 with BMI and waist circumference in white and Hispanic women, but not among black and Asian/Pacific Islander women. On average, each copy of the risk-allele A at rs9939609 was significantly associated with 0.45 kg/m(2) increase in BMI (95% confidence interval (CI): 0.16-0.74; P = 0.004) and 0.97 cm increase in waist circumference (95% CI: 0.21-0.65; P = 0.0002). Similar results were observed for rs8050136. However, we found no significant genetic associations with diabetes risk, either within the full study sample or in any ethnic group. In conclusion, common genetic variants in the intron 1 of FTO gene may confer a modest susceptibility to obesity in an ethnicity-specific manner, but may be unlikely to contribute to a clinically significant diabetes risk.
通过对几个欧洲人群进行全基因组关联分析,FTO基因最近被确定为肥胖症和2型糖尿病的一个易感基因座。我们在美国一个特征明确的绝经后女性多民族队列中,检测了FTO风险等位基因与肥胖症及糖尿病之间的关联。在一项巢式病例对照研究中,我们对来自女性健康倡议观察性研究(WHI-OS)的1517例糖尿病病例和2123例对照,对FTO基因第1内含子中两个最显著相关的单核苷酸多态性(SNP)(rs9939609和rs8050136)进行了基因分型。rs9939609或rs8050136的等位基因频率在四个种族群体中差异很大。rs9939609罕见等位基因A在对照组中的频率,在亚裔/太平洋岛民中(17%)远低于黑人(45%)、白人(40%)和西班牙裔(31%)。我们发现rs9939609与白人和西班牙裔女性的体重指数(BMI)及腰围显著相关,但在黑人和亚裔/太平洋岛民女性中未发现这种关联。平均而言,rs9939609处风险等位基因A的每一个拷贝与BMI显著增加0.45kg/m²相关(95%置信区间(CI):0.16 - 0.74;P = 0.004),与腰围增加0.97cm相关(95%CI:0.21 - 0.65;P = 0.0002)。rs8050136也观察到类似结果。然而,无论是在整个研究样本中还是在任何种族群体中,我们均未发现与糖尿病风险存在显著的遗传关联。总之,FTO基因第1内含子中的常见基因变异可能以种族特异性方式赋予适度的肥胖易感性,但可能不太可能导致临床上显著的糖尿病风险。