Matrix metalloproteinase-9 Gene-1562C>T Gene Polymorphism and Coronary Artery Disease in the Chinese Han Population: A Meta-Analysis of 5468 Subjects

Multiple studies indicate that the matrix metalloproteinase-9 (MMP-9)-1562C>T gene polymorphism may be associated with an increased risk of coronary artery disease (CAD) in the Chinese Han population. However, a clear consensus has yet to be established. A meta-analysis of 5468 subjects from 10 s...

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Published inFrontiers in physiology Vol. 7; p. 212
Main Authors Li, Yan-Yan, Yang, Xin-Xing, Zhou, Yan-Hong, Gong, Ge, Geng, Hong-Yu, Kim, Hyun J., Zhou, Chuan-Wei, Qian, Yun, Wang, Xiang-Ming, Wu, Jun
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 09.06.2016
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Summary:Multiple studies indicate that the matrix metalloproteinase-9 (MMP-9)-1562C>T gene polymorphism may be associated with an increased risk of coronary artery disease (CAD) in the Chinese Han population. However, a clear consensus has yet to be established. A meta-analysis of 5468 subjects from 10 separate studies was performed to explore the possible relationship between the MMP-9-1562C>T gene polymorphism and CAD within the Chinese Han population. Pooled odds ratio (ORs) for the association and the corresponding 95% confidence intervals (CIs) were evaluated by a random or fixed-effect model. Our analysis confirms the association between the MMP-9-1562C>T gene polymorphism and an increased risk of CAD within the Chinese Han population under allelic (OR: 1.60, 95% CI: 1.25-2.04, P = 0.0002), recessive (OR: 3.05, 95% CI: 1.67-5.56, P = 0.0003), dominant (OR: 2.23, 95% CI: 1.49-3.35, P = 0.0001), homozygous (OR: 3.41, 95% CI: 1.87-6.23, P < 0.0001), heterozygous (OR: 2.03, 95% CI: 1.40-2.93, P = 0.0002), and additive genetic models (OR: 1.78, 95% CI: 1.33-2.39, P < 0.0001). In the Chinese Han population, the MMP-9-1562C>T gene polymorphism is correlated with an increased risk of CAD. Therefore, Han Chinese carriers of the -1562T allele may be at an increased risk of CAD.
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This article was submitted to Vascular Physiology, a section of the journal Frontiers in Physiology
Edited by: Alexey Goltsov, Abertay University, UK
Reviewed by: Karen Yvonne Stokes, Louisiana State University Health Sciences Center, USA; Wang Min, Yale University, USA
ISSN:1664-042X
1664-042X
DOI:10.3389/fphys.2016.00212