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首页> 外文期刊>Journal of atherosclerosis and thrombosis. >Apolipoprotein E Epsilon 4 Enhances the Association between the rs2910164 Polymorphism of miR-146a and Risk of Atherosclerotic Cerebral Infarction
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Apolipoprotein E Epsilon 4 Enhances the Association between the rs2910164 Polymorphism of miR-146a and Risk of Atherosclerotic Cerebral Infarction

机译:载脂蛋白E Epsilon 4增强了rs2910164 miR-146a多态性与动脉粥样硬化性脑梗死风险之间的关联

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摘要

Aim : To analyse the relationship between two potentially functional single-nucleotide polymorphisms (SNPs) of the miR-146a gene (rs2910164 and rs57095329) and the risk of atherosclerotic cerebral infarction (ACI). Methods : A total of 297 patients with ACI and 300 matched healthy individuals were enrolled in the study. The miR-146a polymorphism was detected using the polymerase chain reaction–restriction fragment length polymorphism method. Results : A significant difference in the C allele frequency at rs2910164 ( p =0.028) was noted between patients with ACI and control subjects. In contrast, the genotype and allele frequencies of rs57095329 were not statistically associated with ACI. In addition, the decreased expression of miR-146a was significantly more frequent in ACI patients who were ApoEε4 (+) carriers ( p =0.0233), and rs2910164 G>C was intimately associated with the ApoEε4-containing genotype in patients compared with the ApoEε4 (-) carriers ( p =0.0323). Conclusions : Our findings indicated that the C allele of rs2910164 miR-146a is an important risk factor for ACI, and ApoEε4 may function through attenuating miR-146a expression to enhance ACI susceptibility. This study provides new information about the possible relationship between miR-146a and ApoEε4 in the development of ACI, with potentially important therapeutic implications.
机译:目的:分析miR-146a基因的两个潜在功能性单核苷酸多态性(SNP)(rs2910164和rs57095329)与动脉粥样硬化性脑梗塞(ACI)的风险之间的关系。方法:本研究共纳入297例ACI患者和300名健康人。使用聚合酶链反应-限制性片段长度多态性方法检测到miR-146a多态性。结果:ACI患者与对照组之间在rs2910164处的C等位基因频率存在显着差异(p = 0.028)。相比之下,rs57095329的基因型和等位基因频率与ACI没有统计学相关性。此外,与ApoEε4相比,ApoEε4(+)携带者的ACI患者中miR-146a的表达降低更为明显(p = 0.0233),并且rs2910164 G> C与含ApoEε4的基因型密切相关。 (-)个载波(p = 0.0323)。结论:我们的发现表明,rs2910164 miR-146a的C等位基因是ACI的重要危险因素,ApoEε4可能通过减弱miR-146a的表达来增强ACI的敏感性。这项研究提供了有关ACI发生中miR-146a和ApoEε4之间可能关系的新信息,并可能具有重要的治疗意义。

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