Department of Medical Laboratory, Affiliated Hospital of Youjiang Medical University for Nationalities.
Department of Medical Laboratory, Affiliated Hospital of Guilin Medical University.
J Hypertens. 2020 Aug;38(8):1481-1487. doi: 10.1097/HJH.0000000000002413.
Polymorphisms in microRNA genes are related to the risk of ischemic stroke, but the association between miR-34b/c polymorphisms and the risk of ischemic stroke has not been reported.
MiR-34b/c rs2187473 and rs4938723 polymorphisms were genotyped by Snapshot assay among 495 controls and 492 ischemic stroke patients. Expression levels of miR-34b and miR-34c were quantified by real-time PCR. Transcriptional activity of miR-34b/c promoter was measured by luciferase reporter assay.
Rs4938723 was associated with an increased risk of ischemic stroke in our study (CC versus TT: OR = 2.34, 95% CI = 1.47-3.72, P = 0.001; C versus T: OR = 1.37, 95% CI = 1.12-1.68, P = 0.002; CC versus TT + TC: OR = 2.12, 95% CI = 1.37-3.29, P = 0.001). The expression levels of miR-34b and miR-34c were significantly downregulated in cases by contrast with controls (P < 0.05). Further analysis demonstrated that the expression levels of miR-34b and miR-34c were also downregulated in the individuals carrying rs4938723 CC genotype by contrast with that carrying TT + TC genotypes (P < 0.05). The result of luciferase reporter assay showed that rs4938723C allele decreased the transcriptional activity of miR-34b/c promoter compared with rs4938723 T allele.
Our study showed a positive relation between the miR-34b/c rs4938723 polymorphism and the risk of ischemic stroke, which indicated that rs4938723 may be used for ischemic stroke prediction or therapy in the future.
miRNA 基因多态性与缺血性脑卒中风险相关,但 miR-34b/c 多态性与缺血性脑卒中风险的关系尚未报道。
采用Snapshot assay 检测 495 例对照和 492 例缺血性脑卒中患者 miR-34b/c rs2187473 和 rs4938723 多态性。采用实时 PCR 定量检测 miR-34b 和 miR-34c 的表达水平。采用荧光素酶报告基因检测 miR-34b/c 启动子的转录活性。
在本研究中,rs4938723 与缺血性脑卒中风险增加相关(CC 与 TT:OR=2.34,95%CI=1.47-3.72,P=0.001;C 与 T:OR=1.37,95%CI=1.12-1.68,P=0.002;CC 与 TT+TC:OR=2.12,95%CI=1.37-3.29,P=0.001)。与对照组相比,病例组 miR-34b 和 miR-34c 的表达水平显著下调(P<0.05)。进一步分析表明,与 TT+TC 基因型相比,携带 rs4938723 CC 基因型的个体 miR-34b 和 miR-34c 的表达水平也下调(P<0.05)。荧光素酶报告基因检测结果显示,与 rs4938723 T 等位基因相比,rs4938723C 等位基因降低了 miR-34b/c 启动子的转录活性。
本研究表明 miR-34b/c rs4938723 多态性与缺血性脑卒中风险呈正相关,提示 rs4938723 可用于未来缺血性脑卒中的预测或治疗。