Li Yiping, Zhang Yu, Li Xianli, Shi Li, Tao Wenyu, Shi Lei, Yang Man, Wang Xiaoling, Yang Ying, Yao Yufeng
1. Department of Endocrinology and Metabolism, The Second People's Hospital of Yunnan Province & The Fourth Affiliated Hospital of Kunming Medical University, Kunming 650021, Yunnan, China ; 2. Key Laboratory of Fertility Regulation and Eugenics of Minority Research of Yunnan Province, Kunming 650091, Yunnan, China.
3. Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, Yunnan, China.
Int J Med Sci. 2015 Oct 20;12(11):875-80. doi: 10.7150/ijms.12954. eCollection 2015.
Accumulated evidence indicates that microRNA (miRNA or miR) is involved in the development of type 2 diabetes (T2DM). Several studies have shown that single nucleotide polymorphisms (SNPs) located in miRNAs are associated with T2DM in Caucasian populations. The association studies of miRNA's SNPs with T2DM in Asian are rarely reported, and there are distinct genetic differences between Caucasian and Asian populations. The focus of this study, therefore, is the association of T2DM with five SNPs (rs895819 in miR-27a, rs531564 in miR-124a, rs11888095 in miR-128a, rs3820455 in miR-194a and rs2910164 in miR-146a) located in five miRNAs in a Han Chinese population. A total of 738 subjects with T2DM and 610 non-diabetic subjects were genotyped using the TaqMan method. Next, the associations between the five SNPs with T2DM and individual metabolic traits were evaluated. Our data showed that the C allele of rs531564 in miR-124a may protect against T2DM (P=0.009, OR=0.758; 95%CI: 0.616-0.933). Conversely, the C allele of rs2910164 in miR-146a may increase the risk of developing T2DM (P<0.001, OR=1.459; 95%CI: 1.244-1.712). However, these five SNPs did not exhibit significant associations with individual metabolic traits in either the T2DM or non-diabetic groups. Our results revealed that genetic variations in miRNAs were associated with T2DM susceptibility in a Han Chinese population, and these results highlight the need to study the functional effects of these variants in miRNAs on the risk of developing T2DM.
越来越多的证据表明,微小RNA(miRNA或miR)参与了2型糖尿病(T2DM)的发生发展。多项研究表明,位于miRNA中的单核苷酸多态性(SNP)与白种人群中的T2DM相关。关于miRNA的SNP与亚洲人群T2DM的关联研究鲜有报道,而且白种人和亚洲人群之间存在明显的遗传差异。因此,本研究的重点是在汉族人群中研究T2DM与位于5种miRNA中的5个SNP(miR-27a中的rs895819、miR-124a中的rs531564、miR-128a中的rs11888095、miR-194a中的rs3820455和miR-146a中的rs2910164)的关联。使用TaqMan方法对总共738例T2DM患者和610例非糖尿病患者进行基因分型。接下来,评估这5个SNP与T2DM及个体代谢特征之间的关联。我们的数据显示,miR-124a中rs531564的C等位基因可能对T2DM具有保护作用(P=0.009,OR=0.758;95%CI:0.616-0.933)。相反,miR-146a中rs2910164的C等位基因可能增加患T2DM的风险(P<0.001,OR=1.459;95%CI:1.244-1.712)。然而,在T2DM组或非糖尿病组中,这5个SNP与个体代谢特征均未表现出显著关联。我们的结果表明,miRNA中的基因变异与汉族人群的T2DM易感性相关,这些结果凸显了研究miRNA中这些变异对T2DM发病风险的功能影响的必要性。