| Literature DB >> 29498555 |
Zhou Zheng1, Xinwei He1, Min Zhu2, Xiaoping Jin1, Cai Li1, Feng Zhu1, Chenling Lv1, Weiling Li1, Xiaofei Hu1, Wanfeng Wang1, Feng Wang1.
Abstract
Tissue inhibitor of metalloproteinases (TIMPs) are endogenous inhibitors of matrix metalloproteinases that are involved in normal cellular processes and in the development and progression of atherosclerosis. Our purpose was to evaluate the polymorphisms of the TIMP-3 genes for their associations with carotid plaques or with serum protein levels in the Han Chinese population. Two promoter variants, -915A/G (rs2234921) and -1296T/C (rs9619311), were genotyped in 548 subjects with no plaques, 462 subjects with echogenic plaques, and 427 subjects with mixture plaques. The serum TIMP-3 levels were measured using an enzyme-linked immunosorbent assay (ELISA). There was a strong linkage disequilibrium between -1296T/C and -915A/G (D' = 1.0, r2 = 0.991). The individuals with the genotype (TC+CC) were 1.8 times more likely to have mixture plaques than the individuals with the TT genotype (P = 0.001, OR: 1.836, 95%CI: 1.269-2.665). The frequency of the C allele in the mixture plaque group was significantly higher than in the no plaque group (P = 0.009, CI: 1.119-2.187). We observed a significant elevation of the TIMP-3 levels in the serum of patients affected with mixture plaques compared to those with no plaques (P = 0.013). The current data suggest that genetic variation in the TIMP-3 genes may contribute to individual differences in mixture plaque susceptibility in the Han Chinese population.Entities:
Keywords: Tissue inhibitor of metalloproteinases-3; carotid atherosclerosis; cerebrovascular disease; linkage disequilibrium; single-nucleotide polymorphism
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Year: 2018 PMID: 29498555 DOI: 10.1080/00207454.2018.1436544
Source DB: PubMed Journal: Int J Neurosci ISSN: 0020-7454 Impact factor: 2.292