Huang Xiao-Ya, Han Li-Ya, Huang Xiang-Dong, Guan Chao-Hong, Mao Xin-Lei, Ye Zu-Sen
a Department of Neurology , Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University , Wenzhou , China.
b Department of Neurology , The First Affiliated Hospital of Wenzhou Medical University , Wenzhou , China.
Int J Neurosci. 2016 Oct;126(10):936-41. doi: 10.3109/00207454.2015.1088013. Epub 2015 Sep 22.
Little is known about the impact of the 5A/6A polymorphism of matrix metalloproteinase-3 (MMP-3) on recurrence of atherosclerotic ischemic stroke in Chinese. The aim of this study was to investigate the association of MMP-3 serum level and 5A/6A genetic polymorphism with the recurrence of atherosclerotic ischemic stroke in the Chinese Han population. We analyzed 106 large artery atherosclerosis (LAA) recurrent ischemic stroke patients and 545 LAA first onset ischemic stroke patients from January 2009 to June 2014. Serum MMP-3 concentrations were measured with an enzyme-linked immunosorbent assay. The genotypes of MMP-3 promoter polymorphism (-1171 5A/6A) were determined using polymerase chain reaction-restriction fragment length polymorphism. The frequencies of MMP-3 5A/6A+5A/5A (32.08% vs. 21.47%, p = 0.02) genotype and 5A (16.98% vs. 11.01%, p = 0.01) allele in the recurrent group was significantly higher than those in the first onset group. After adjustment for vascular risk factors, multivariate logistic regression analysis suggested that the MMP-3 5A/6A+5A/5A genotype was an independent risk factor for LAA recurrent ischemic stroke (odds ratio [OR], 1.74; 95% confidence interval [CI], 1.09-2.79, p = 0.021). No significant difference was observed for the MMP-3 serum concentrations between the recurrent group and the first onset group (22.23 ± 8.31 vs. 21.49 ± 7.89 ng/ul, t = 0.88, p = 0.38). The MMP-3 (-1171 5A/6A) polymorphism may contribute to LAA recurrent ischemic stroke susceptibility. Analysis of 5A/6A polymorphism in MMP-3 may identify patients at higher risk for LAA ischemic stroke recurrence, who may be selected for intensive preventive therapy.
在中国,基质金属蛋白酶-3(MMP-3)的5A/6A多态性对动脉粥样硬化性缺血性脑卒中复发的影响鲜为人知。本研究旨在探讨中国汉族人群中MMP-3血清水平和5A/6A基因多态性与动脉粥样硬化性缺血性脑卒中复发的关系。我们分析了2009年1月至2014年6月期间的106例大动脉粥样硬化(LAA)复发性缺血性脑卒中患者和545例LAA首发缺血性脑卒中患者。采用酶联免疫吸附测定法检测血清MMP-3浓度。使用聚合酶链反应-限制性片段长度多态性方法确定MMP-3启动子多态性(-1171 5A/6A)的基因型。复发性组中MMP-3 5A/6A+5A/5A基因型(32.08%对21.47%,p = 0.02)和5A等位基因(16.98%对11.01%,p = 0.01)的频率显著高于首发组。在调整血管危险因素后,多因素逻辑回归分析表明,MMP-3 5A/6A+5A/5A基因型是LAA复发性缺血性脑卒中的独立危险因素(比值比[OR],1.74;95%置信区间[CI],1.09-2.79,p = 0.021)。复发性组和首发组之间的MMP-3血清浓度无显著差异(22.23±8.31对21.49±7.89 ng/ul,t = 0.88,p = 0.38)。MMP-3(-1171 5A/6A)多态性可能与LAA复发性缺血性脑卒中易感性有关。分析MMP-3中的5A/6A多态性可能有助于识别LAA缺血性脑卒中复发风险较高的患者,这些患者可被选择进行强化预防性治疗。