Laboratory for Endocrinology and Metabolism, RIKEN Center for Genomic Medicine, Yokohama, Japan.
J Hum Genet. 2013 Jul;58(7):490-3. doi: 10.1038/jhg.2013.28. Epub 2013 Apr 18.
By an association mapping for the candidate locus in chromosome 21q, rs3746876 within KCNJ15 was shown to be associated with type 2 diabetes in Japanese populations. However, the association of rs3746876 with type 2 diabetes has not been validated in an independent cohort. The aim of the present study was to ascertain the association of rs3746876 with type 2 diabetes in an independent larger Japanese sample. We genotyped 7885 Japanese participants (4967 individuals with type 2 diabetes and 2918 control individuals) for rs3746876 with polymerase-chain reaction-invader assay. The association of rs3746876 with type 2 diabetes was examined by using logistic regression analysis. Quantitative traits analyses for homeostasis model assessment (HOMA) of β-cell function, HOMA of insulin resistance, fasting plasma glucose, fasting immunoreactive insulin and body mass index (BMI) were performed in control individuals by using multiple-linear regression analysis. We observed a significant association of rs3746876-T with type 2 diabetes (P=0.0281, odds ratio (OR)=0.82, 95% confidence interval (CI, 0.68-0.98)), but the direction of effect was opposite to that in the original report. The association of rs3746876 with type 2 diabetes was more significant in obese patients (BMI ≥ 25 kg m(-2), P=0.0025, OR=0.62, 95% CI, 0.45-0.84). We did not observe significant association of rs3746876 with any of the quantitative traits in the control individuals. We could not replicate the original finding for the association of rs3746876 with type 2 diabetes, although rs3746876 was significantly associated with obese type 2 diabetes in the present Japanese population.
通过对 21 号染色体候选基因座的关联映射,发现 KCNJ15 内的 rs3746876 与日本人群的 2 型糖尿病相关。然而,rs3746876 与 2 型糖尿病的关联在独立队列中尚未得到验证。本研究旨在在更大的日本独立样本中确定 rs3746876 与 2 型糖尿病的关联。我们使用聚合酶链反应-入侵检测法对 7885 名日本参与者(4967 名 2 型糖尿病患者和 2918 名对照个体)进行 rs3746876 的基因分型。使用逻辑回归分析检查 rs3746876 与 2 型糖尿病的关联。在对照个体中,使用多元线性回归分析对稳态模型评估(HOMA)的β细胞功能、胰岛素抵抗的 HOMA、空腹血糖、空腹免疫反应性胰岛素和体重指数(BMI)进行定量特征分析。我们观察到 rs3746876-T 与 2 型糖尿病显著相关(P=0.0281,比值比(OR)=0.82,95%置信区间(CI)0.68-0.98)),但效应方向与原始报告相反。在肥胖患者(BMI≥25kg/m2,P=0.0025,OR=0.62,95%CI,0.45-0.84)中,rs3746876 与 2 型糖尿病的关联更为显著。我们在对照个体中没有观察到 rs3746876 与任何定量特征之间存在显著关联。尽管 rs3746876 与本日本人群的肥胖 2 型糖尿病显著相关,但我们无法复制 rs3746876 与 2 型糖尿病关联的原始发现。