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ENPP1 K121Q 多态性与中国人群 2 型糖尿病:一项包含 11855 例个体的荟萃分析。

ENPP1 K121Q polymorphism and type 2 diabetes mellitus in the Chinese population: a meta-analysis including 11,855 subjects.

机构信息

Department of Geriatrics, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.

出版信息

Metabolism. 2012 May;61(5):625-33. doi: 10.1016/j.metabol.2011.10.002. Epub 2011 Dec 2.

Abstract

Ectoenzyme nucleotide pyrophosphate phosphodiesterase 1 (ENPP1) K121Q gene polymorphism has been suggested to be associated with the increased risk of developing type 2 diabetes mellitus (T2D), but relevant research results are still contradictory. To explore the relationship between ENPP1 K121Q gene polymorphism and T2D in the Chinese population, a meta-analysis was performed. Fourteen independent studies involving 11 855 subjects were retrieved from electronic databases. The pooled odds ratio (ORs) for the distribution of Q allele frequency of the ENPP1 K121Q gene and its corresponding 95% confidence interval (95% CI) were assessed using a random-effects model. Under an allelic model of inheritance, the distribution of Q allele frequency was 0.107 for the T2D group and 0.093 for the control group. The pooled OR for the distribution of Q allele frequency of ENPP1 K121Q gene was 1.29 (95% CI, 1.09-1.53; P(heterogeneity) = .006; I(2) = 55.6%). There was a significant association between ENPP1 K121Q gene polymorphism and T2D in the Chinese population (P = .003). Under a dominant model of inheritance, the KQ + QQ/KK value was 0.259 for the T2D group and 0.220 for the control group. The pooled OR for the KQ + QQ/KK value was 1.51 (95% CI, 1.20-1.91; P(heterogeneity) < .0001; I(2) = 71.8%). The association between ENPP1 K121Q gene polymorphism and T2D in the Chinese population followed a dominant model of inheritance (P = .0005). In the Chinese population, the ENPP1 K121Q gene polymorphism was implied to be involved with T2D susceptibility. People with the Q allele of the ENPP1 K121Q gene might be predisposed to T2D.

摘要

外切核苷酸焦磷酸酶/磷酸二酯酶 1(ENPP1)K121Q 基因多态性与 2 型糖尿病(T2D)的发病风险增加有关,但相关研究结果仍存在争议。为探讨 ENPP1 K121Q 基因多态性与中国人群 T2D 的关系,进行了荟萃分析。从电子数据库中检索到 14 项独立的研究,共涉及 11855 例受试者。采用随机效应模型评估 ENPP1 K121Q 基因 Q 等位基因频率分布的合并优势比(OR)及其相应的 95%置信区间(95%CI)。在遗传的等位基因模型下,T2D 组 Q 等位基因频率分布为 0.107,对照组为 0.093。ENPP1 K121Q 基因 Q 等位基因频率分布的合并 OR 为 1.29(95%CI,1.09-1.53;P(异质性)=.006;I2=55.6%)。ENPP1 K121Q 基因多态性与中国人群 T2D 显著相关(P=.003)。在显性遗传模型下,T2D 组 KQ+QQ/KK 值为 0.259,对照组为 0.220。KQ+QQ/KK 值的合并 OR 为 1.51(95%CI,1.20-1.91;P(异质性)<.0001;I2=71.8%)。ENPP1 K121Q 基因多态性与中国人群 T2D 之间存在显性遗传模式的关联(P=.0005)。在中国人群中,ENPP1 K121Q 基因多态性与 T2D 易感性有关。携带 ENPP1 K121Q 基因 Q 等位基因的人可能易患 T2D。

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