Zhao Jing, Bai Yun, Jin Lei, Weng Yingfeng, Wang Yujie, Wu Hui, Li Xia, Huang Ying, Wang Shengyue
Department of Neurology, Minhang district central hospital, Shanghai, China.
Shanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center at Shanghai, Shanghai, China.
PLoS One. 2017 Feb 24;12(2):e0172709. doi: 10.1371/journal.pone.0172709. eCollection 2017.
Vascular endothelial growth factor (VEGF) plays critical roles in angiogenesis and vasculogenesis, which are associated with post-stroke functional recovery. However, the effects of the VEGFA polymorphisms on the outcome of ischemic stroke (IS) have been rarely reported. We therefore investigated the associations of +936C/T variant (rs3025039) with the susceptibilities and the 90-day outcomes from 494 IS patients and 337 healthy controls in Chinese population through the establishment of logistic multivariate regression model. Stroke severity at admission and outcome of 90 days were respectively assessed according to the National Institutes of Health Stroke Scale and the modified Rankin Scale. The analysis showed that there were no significant associations of the rs3025039 genotypes with the susceptibility (P = 0.229) and the severity (P = 0.734). However, when we divided the 308 IS patients into two groups according to the different outcomes, we found that the rs3025039 TC+TT genotype significantly increased the risk of poor recovery [adjusted odds ratio (OR), 1.99; 95% confidence interval (CI), 1.18-3.37]. Interestingly, we observed another 3'UTR variant, +1451C/T (rs3025040), exhibited strong linkage disequilibrium (r2 = 1.0) with +936C/T and was located in a predicted microRNA-binding site. The rs3025040 T allele significantly decreased the luciferase activities in four cell lines, which indicated a potential disruption of the miRNA-mRNA interaction that would result in lower VEGF expression levels. Our data suggested that the +936C/T variants significantly increased the risk of poorer stroke outcome by affecting the bindings of miR-199a and miR-199b to VEGF mRNA at the rs30250340 polymorphic site.
血管内皮生长因子(VEGF)在血管生成和血管发生过程中发挥着关键作用,而这两个过程与中风后的功能恢复相关。然而,VEGFA基因多态性对缺血性中风(IS)预后的影响鲜有报道。因此,我们通过建立逻辑多元回归模型,在中国人群的494例IS患者和337例健康对照中,研究了+936C/T变异(rs3025039)与易感性及90天预后的相关性。根据美国国立卫生研究院卒中量表和改良Rankin量表分别评估入院时的中风严重程度和90天的预后。分析表明,rs3025039基因型与易感性(P = 0.229)和严重程度(P = 0.734)均无显著相关性。然而,当我们根据不同预后将308例IS患者分为两组时,发现rs3025039 TC+TT基因型显著增加了恢复不良的风险[调整优势比(OR)为1.99;95%置信区间(CI)为1.18 - 3.37]。有趣的是,我们观察到另一个3'UTR变异+1451C/T(rs3025040)与+936C/T表现出强连锁不平衡(r2 = 1.0),且位于一个预测的微小RNA结合位点。rs3025040 T等位基因在四种细胞系中显著降低了荧光素酶活性,这表明可能破坏了微小RNA - mRNA相互作用,从而导致VEGF表达水平降低。我们的数据表明,+936C/T变异通过影响miR - 199a和miR - 199b在rs30250340多态性位点与VEGF mRNA的结合,显著增加了中风预后较差的风险。