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基质金属蛋白酶基因多态性与中国汉族人群急性缺血性脑卒中的相关性
Authors Li A, Han T, Li Y, Yang G, Zhang Y, Huang Y, Zhou B, Song G, He Y
Received 12 November 2022
Accepted for publication 2 February 2023
Published 20 February 2023 Volume 2023:16 Pages 619—629
DOI https://doi.org/10.2147/IJGM.S395416
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Woon-Man Kung
Background and Purpose: Studies have shown that matrix metalloproteinase (MMP-2,3,9) plays an important role in the pathologic process of ischemic stroke (IS). The aim of this study was to investigate the relationship between C1306T, 1612– 5A/6A, C-1562T polymorphisms of MMP -2,3,9 genes and IS in Chinese Han population.
Methods: The polymorphisms of MMP -2(C1306T), − 3(1612– 5A/6A), − 9(C-1562T) gene were detected by PCR-RFLP and SNaPshot sequencing. Then, stratified analysis was used to study the relationship between IS subtypes and MMP-2,3,9 polymorphisms.
Results: For the MMP-2 gene C1306T polymorphism, TT genotype and T allele were significantly associated with a reduced risk of IS (P = 0.015, P = 0.003, respectively). T allele was significantly associated with a reduced risk of small artery occlusion (SAO) subtype compared with the control group (P = 0.012, OR = 0.550, 95% CI = 0.065– 1.291). For the MMP-3 gene-1612 (5A/6A) polymorphism, 5A/5A genotype was significantly increased in the IS group (P = 0.011, OR = 0.370, 95% CI = 0.168– 0.814), especially in the large-artery atherosclerosis (LAA) subtype (P = 0.001, OR = 2.345) as compared to the control group.
Conclusion: Our study suggested that the T allele of MMP -2 may be a protective factor of IS, especially in SAO subtype, while the 5A/5A gene of MMP -3 may increase the risk of IS, especially in LAA subtype in Chinese Han population.
Keywords: ischemic stroke, matrix metalloproteinase, polymorphism, association study