Li Xiaoying, Wang Zhenzhen, Liu Yan, Zhang Ruyou, Guo Xijuan, Liu Wei, Ning Chunping, Sun Litao, Tian Jiawei
Department of Ultrasound, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150081, People's Republic of China.
J Mol Neurosci. 2014 Apr;52(4):461-6. doi: 10.1007/s12031-013-0110-9. Epub 2013 Sep 7.
Cerebral atherosclerosis vascular stenosis is a common etiology for ischemic stroke and a major factor in recurrent stroke and vascular mortality. Recent studies suggest that renalase plays a role in hypertension and ischemic stroke, and may be involved in atherosclerosis. The aim of the present study was to investigate whether there were correlations between single-nucleotide polymorphisms (SNPs) in the renalase gene and severity of intracranial cerebral atherosclerotic vascular stenosis in ischemic stroke patients as determined by imaging. A total of 212 ischemic stroke patients and 244 healthy controls from the north Chinese Han population were enrolled in this study. Polymerase chain reaction and ligase detection reaction were used for SNP analysis. We classified the case samples by severity of the intracranial cerebral atherosclerotic vascular stenosis. Allele, genotype, and haplotype were analyzed in cases and controls, and logistic regression was used to adjust for bias due to conventional stroke risk factors. The allele and the genotype of rs10887800 in the renalase gene were both associated with severe intracranial cerebral atherosclerotic vascular stenosis (p = 0.013 and p = 0.049, respectively). No association was observed with severity for SNP rs2576178 or SNP rs2296545. Our findings show that the SNP rs10887800 in the renalase gene is closely associated with severe intracranial cerebral atherosclerotic vascular stenosis in ischemic stroke patients of north Chinese Han origin.
脑动脉粥样硬化性血管狭窄是缺血性卒中的常见病因,也是复发性卒中和血管性死亡的主要因素。最近的研究表明,肾酶在高血压和缺血性卒中中起作用,并且可能参与动脉粥样硬化。本研究的目的是调查肾酶基因单核苷酸多态性(SNP)与缺血性卒中患者颅内脑动脉粥样硬化性血管狭窄严重程度之间是否存在相关性,该严重程度通过影像学确定。本研究纳入了212例来自中国北方汉族人群的缺血性卒中患者和244例健康对照。采用聚合酶链反应和连接酶检测反应进行SNP分析。我们根据颅内脑动脉粥样硬化性血管狭窄的严重程度对病例样本进行分类。对病例组和对照组进行等位基因、基因型和单倍型分析,并使用逻辑回归调整传统卒中危险因素导致的偏差。肾酶基因中rs10887800的等位基因和基因型均与严重颅内脑动脉粥样硬化性血管狭窄相关(分别为p = 0.013和p = 0.049)。未观察到SNP rs2576178或SNP rs2296545与严重程度的关联。我们的研究结果表明,肾酶基因中的SNP rs10887800与中国北方汉族缺血性卒中患者的严重颅内脑动脉粥样硬化性血管狭窄密切相关。