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日本受试者中2型糖尿病患者胰腺β细胞功能相关基因变异的关联研究。

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.

作者信息

Yokoi Norihide, Kanamori Masao, Horikawa Yukio, Takeda Jun, Sanke Tokio, Furuta Hiroto, Nanjo Kishio, Mori Hiroyuki, Kasuga Masato, Hara Kazuo, Kadowaki Takashi, Tanizawa Yukio, Oka Yoshitomo, Iwami Yukiko, Ohgawara Hisako, Yamada Yuichiro, Seino Yutaka, Yano Hideki, Cox Nancy J, Seino Susumu

机构信息

Division of Cellular and Molecular Medicine, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.

出版信息

Diabetes. 2006 Aug;55(8):2379-86. doi: 10.2337/db05-1203.

Abstract

Because impaired insulin secretion is characteristic of type 2 diabetes in Asians, including Japanese, the genes involved in pancreatic beta-cell function are candidate susceptibility genes for type 2 diabetes. We examined the association of variants in genes encoding several transcription factors (TCF1, TCF2, HNF4A, ISL1, IPF1, NEUROG3, PAX6, NKX2-2, NKX6-1, and NEUROD1) and genes encoding the ATP-sensitive K(+) channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) with type 2 diabetes in a Japanese cohort of 2,834 subjects. The exon 16 -3c/t variant rs1799854 in ABCC8 showed a significant association (P = 0.0073), and variants in several genes showed nominally significant associations (P < 0.05) with type 2 diabetes. Although the E23K variant rs5219 in KCNJ11 showed no association with diabetes in Japanese (for the K allele, odds ratio [OR] 1.08 [95% CI 0.97-1.21], P = 0.15), 95% CI around the OR overlaps in meta-analysis of European populations, suggesting that our results are not inconsistent with the previous studies. This is the largest association study so far conducted on these genes in Japanese and provides valuable information for comparison with other ethnic groups.

摘要

由于胰岛素分泌受损是包括日本人在内的亚洲人2型糖尿病的特征,参与胰腺β细胞功能的基因是2型糖尿病的候选易感基因。我们在一个由2834名受试者组成的日本队列中,研究了编码几种转录因子(TCF1、TCF2、HNF4A、ISL1、IPF1、NEUROG3、PAX6、NKX2-2、NKX6-1和NEUROD1)的基因以及编码ATP敏感性钾(K+)通道亚基Kir6.2(KCNJ11)和SUR1(ABCC8)的基因中的变异与2型糖尿病的关联。ABCC8基因外显子16 -3c/t变异rs1799854显示出显著关联(P = 0.0073),几个基因中的变异与2型糖尿病显示出名义上的显著关联(P < 0.05)。尽管KCNJ11基因中的E23K变异rs5219在日本人中与糖尿病无关联(对于K等位基因,优势比[OR]为1.08[95%CI 0.97 - 1.21],P = 0.15),但在欧洲人群的荟萃分析中,OR周围的95%CI有重叠,这表明我们的结果与先前的研究并非不一致。这是迄今为止在日本人中对这些基因进行的最大规模关联研究,为与其他种族群体进行比较提供了有价值的信息。

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