Department of Nutrition and Food Hygiene, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan, PR China.
Diabetes Metab Res Rev. 2010 Feb;26(2):128-32. doi: 10.1002/dmrr.1066.
Recently, a genome-wide association study identified a strong association between the fat mass- and obesity-associated rs9939609 single nucleotide polymorphism (SNP) and the risk of obesity in European population. However, the results in Chinese population were reported to be contradictory. Therefore, our aim was to examine whether this SNP is associated with obesity and newly diagnosed type 2 diabetes (T2D) in Chinese population.
We genotyped rs9939609 in 2587 subjects [obesity 243, overweight 976, normal weight 1368 or newly diagnosed T2D 877, impaired glucose regulation 305, normal glucose tolerance (NGT) 1405] using an allelic discrimination assay-by-design TaqMan method on ABI7900HT. We analysed associations of the rs9939609 SNP with obesity and newly diagnosed T2D through Logistic regression analysis.
In obesity case-control study, we found that the A allele was strongly associated with obesity and overweight. The odds ratios for the allele A versus T were 1.447 for Obesity versus normal weight (95% CI 1.104-1.896, p = 0.007) and 1.363 for Overweight versus normal weight (95% CI 1.149-1.617, p < 0.0001). In T2D case-control study, the odds ratios for the allele A versus T were 1.305 for T2D versus NGT (95% CI 1.097-1.552, p = 0.003) and 1.280 for combined T2D and impaired glucose regulation (IGR) versus NGT (95% CI 1.089-1.503, p = 0.003). The associations of the A allele with T2D and combined T2D and IGR remained significant with adjustment for age, sex and body mass index (BMI).
The fat mass- and obesity-associated gene rs9939609 SNP is strongly associated with risk of obesity and newly diagnosed T2D in the Chinese population.
最近,一项全基因组关联研究发现,脂肪量和肥胖相关的 rs9939609 单核苷酸多态性(SNP)与欧洲人群肥胖风险之间存在强烈关联。然而,中国人群的研究结果存在争议。因此,我们的目的是在中国人群中研究该 SNP 是否与肥胖和新诊断的 2 型糖尿病(T2D)相关。
我们使用 TaqMan 等位基因鉴别分析设计的 ABI7900HT 对 2587 例受试者(肥胖 243 例,超重 976 例,正常体重 1368 例,新诊断的 T2D 877 例,糖耐量受损 305 例,正常葡萄糖耐量(NGT)1405 例)进行 rs9939609 基因分型。我们通过 Logistic 回归分析研究 rs9939609 SNP 与肥胖和新诊断的 T2D 的相关性。
在肥胖病例对照研究中,我们发现 A 等位基因与肥胖和超重密切相关。等位基因 A 与 T 的比值比(OR)分别为肥胖与正常体重(95%CI:1.104-1.896,p=0.007)和超重与正常体重(95%CI:1.149-1.617,p<0.0001)的 1.447 和 1.363。在 T2D 病例对照研究中,等位基因 A 与 T 的比值比(OR)分别为 T2D 与 NGT(95%CI:1.097-1.552,p=0.003)和 T2D 合并糖耐量受损(IGR)与 NGT(95%CI:1.089-1.503,p=0.003)的 1.305 和 1.280。在调整年龄、性别和体重指数(BMI)后,A 等位基因与 T2D 和 T2D 合并 IGR 的相关性仍然显著。
脂肪量和肥胖相关基因 rs9939609 SNP 与中国人群肥胖和新诊断的 T2D 风险密切相关。