PMID- 28843428 OWN - NLM STAT- MEDLINE DCOM- 20180522 LR - 20221207 IS - 1872-6240 (Electronic) IS - 0006-8993 (Linking) VI - 1674 DP - 2017 Nov 1 TI - Association of matrix metalloproteinase-3 gene 5A/6A polymorphism with the recurrence of ischemic stroke: A prospective observational study. PG - 55-61 LID - S0006-8993(17)30345-1 [pii] LID - 10.1016/j.brainres.2017.08.009 [doi] AB - Studies have demonstrated that matrix metalloproteinase-3 (MMP-3) is involved in the development and progression of atherosclerosis. However, there is no information available on the association of MMP-3 5A/6A polymorphism with recurrent ischemic stroke (IS) in different IS subtypes. We investigated the potential associations between MMP-3 serum level and -1171 5A/6A polymorphism and the recurrence of IS in a Chinese population. Consecutive acute first-ever IS patients were enrolled between August 2008 and October 2013. The genotypes of MMP-3 5A/6A polymorphism were determined using polymerase chain reaction-restriction fragment length polymorphism. IS recurrence was monitored after the index event and multivariate Cox proportional hazards model was constructed to identify factors related to future IS recurrence. A total of 1282 eligible patients were enrolled. During a 2-year follow-up period, 157 (12.25%) patients had recurrent events. MMP-3 level was significantly higher in patients with 5A/6A or 5A/5A genotype (22.72+/-7.29ng/ul) than in patients with 6A/6A genotype (20.48+/-7.58ng/ul), P<0.001. No interaction between MMP-3 5A/6A polymorphism and the risk of recurrence in total IS patients was found. The variant 5A/6A+5A/5A genotype and the 5A allele were significantly associated with a high risk of recurrence for large-artery atherosclerosis (LAA) (multivariate-adjusted, P=0.002, 0.001, respectively), but not for small-artery occlusion and cardioembolism. Our finding showed that MMP-3 5A/6A may be a useful biomarker for predicting recurrence for LAA stroke patients and 5A allele carrier may bear a higher risk of recurrence among patients with the subtype of LAA. CI - Copyright (c) 2017. Published by Elsevier B.V. FAU - Huang, Xiaoya AU - Huang X AD - Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Ye, Qiang AU - Ye Q AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Zhang, Zheng AU - Zhang Z AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Huang, Xiangdong AU - Huang X AD - Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Zhu, Zhenguo AU - Zhu Z AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Chen, Yanyan AU - Chen Y AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Li, Jia AU - Li J AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Chen, Siyan AU - Chen S AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Xia, Niange AU - Xia N AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Mao, Xinlei AU - Mao X AD - Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. FAU - Han, Liya AU - Han L AD - Department of Neurology, Wenzhou Central Hospital & Dingli Clinical Institute of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. Electronic address: wzeyhly@126.com. FAU - Ye, Zusen AU - Ye Z AD - Department of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China. Electronic address: zusenye@163.com. LA - eng PT - Journal Article PT - Observational Study DEP - 20170824 PL - Netherlands TA - Brain Res JT - Brain research JID - 0045503 RN - EC 3.4.24.17 (MMP3 protein, human) RN - EC 3.4.24.17 (Matrix Metalloproteinase 3) SB - IM MH - Aged MH - Asian People/genetics MH - Atherosclerosis/genetics/physiopathology MH - Brain Ischemia/enzymology/*genetics MH - Cerebral Infarction/genetics MH - China MH - Female MH - Follow-Up Studies MH - Gene Frequency MH - Genetic Predisposition to Disease MH - Humans MH - Male MH - Matrix Metalloproteinase 3/*genetics/*metabolism MH - Middle Aged MH - Polymorphism, Single Nucleotide MH - Promoter Regions, Genetic MH - Prospective Studies MH - Recurrence MH - Stroke/epidemiology/*genetics OTO - NOTNLM OT - Genotype OT - Ischemic stroke OT - Matrix metalloproteinase OT - Polymorphism OT - Recurrence EDAT- 2017/08/28 06:00 MHDA- 2018/05/23 06:00 CRDT- 2017/08/28 06:00 PHST- 2017/05/24 00:00 [received] PHST- 2017/07/19 00:00 [revised] PHST- 2017/08/09 00:00 [accepted] PHST- 2017/08/28 06:00 [pubmed] PHST- 2018/05/23 06:00 [medline] PHST- 2017/08/28 06:00 [entrez] AID - S0006-8993(17)30345-1 [pii] AID - 10.1016/j.brainres.2017.08.009 [doi] PST - ppublish SO - Brain Res. 2017 Nov 1;1674:55-61. doi: 10.1016/j.brainres.2017.08.009. Epub 2017 Aug 24.