Associations of miR-146a, miR-149, miR-196a2, and miR-499 Polymorphisms with Ischemic Stroke in the Northern Chinese Han Population

被引:13
作者
Zhu, Xiaoyan [1 ]
Hou, Rongyao [2 ]
Ma, Aijun [3 ]
Yang, Shaonan [3 ]
Pan, Xudong [3 ]
机构
[1] Qingdao Univ, Affiliated Hiser Hosp, Dept Crit Care Med, Qingdao, Shandong, Peoples R China
[2] Qingdao Univ, Affiliated Hiser Hosp, Dept Neurol, Qingdao, Shandong, Peoples R China
[3] Qingdao Univ, Affiliated Hosp, Dept Neurol, Qingdao, Shandong, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2018年 / 24卷
关键词
Adams-Stokes Syndrome; Genes; vif; MicroRNAs; CORONARY-ARTERY-DISEASE; GENETIC POLYMORPHISMS; MICRORNA; RISK; ATHEROSCLEROSIS; CANCER; MIRNA; MECHANISMS; EXPRESSION; INFARCTION;
D O I
10.12659/MSM.909935
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Recently, miR-146a C>G, miR-149 T>C, miR-196a2 T>C and miR-499 A>G polymorphisms have been associated with susceptibility to many diseases, including ischemic stroke (IS). However, results have been reported inconsistency in IS, especially in the Chinese population. This study aimed to investigate the polymorphisms of the 4 miRNAs and IS risk in the Chinese population. Material/Methods: We used a case-control study to explore these associations in 396 patients with IS and 378 healthy controls. According to TOAST standards, the selected patients were divided into subgroups: the large artery atherosclerosis (LAA) subgroup and the small artery occlusion (SAO) subgroup. The method of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to detect the genotypes. Results: The miR-146a C>G polymorphism was remarkably different (CC vs. CG+GG: P=0.027; CC+CG vs. GG: P=0.020; C vs. G: P=0.006). The miR-149 T>C polymorphism was also remarkably different (TT vs. TC+CC: P=0.017; TT+TC vs. CC: P=0.020; T vs. C: P=0.004). The miR-146a and miR-149 polymorphisms were also remarkably different in the LAA subgroup (P<0.05). However, we did not find an association of miR-196a2 T>C or miR-499 A>G polymorphisms with IS (P>0.05); we did not find any association in the LAA subgroup or the SAO subgroup (P>0.05). Conclusions: Our study suggested that miR-146a C>G and miR-149 T>C polymorphisms might remarkably increase the risk of IS, which might be mainly associated with an increased risk in LAA stroke; however, the miR-196a2 T>C and miR-499 A>G polymorphisms might not be associated with IS risk in the northern Chinese Han population.
引用
收藏
页码:7366 / 7374
页数:9
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