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首页> 外文期刊>Medicine. >Tissue Factor Pathway Inhibitor-2 Gene Polymorphisms Associate With Coronary Atherosclerosis in Chinese Population
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Tissue Factor Pathway Inhibitor-2 Gene Polymorphisms Associate With Coronary Atherosclerosis in Chinese Population

机译:组织因子途径抑制剂-2基因多态性与中国人口冠状动脉粥样硬化伴

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Tissue factor pathway inhibitor-2 (TFPI-2) may play critical roles in the pathogenesis of atherosclerosis. In this study, we aimed to investigate the association between TFPI-2 gene polymorphisms and coronary atherosclerosis. Four hundred and seven patients with coronary atherosclerosis and 306 individuals with normal coronary artery were enrolled in the present study. Nine single-nucleotide polymorphisms (SNPs) (rs3763473, rs59805398, rs60215632, rs59999573, rs59740167, rs34489123, rs4517, rs4264, and rs4271) were detected with polymerase chain reaction-direct sequencing method. Severity of coronary atherosclerosis was assessed by Gensini score. After the baseline investigation, patients with coronary atherosclerosis were followed up for incidence of cardiovascular events (CVEs). Eight SNPs were in accordance with the Hardy–Weinberg equilibrium, and 8 haplotypes were constructed based on rs59999573, rs59740167, and rs34489123 after linkage disequilibrium and haplotype analysis. Two SNPs (rs59805398 and rs34489123) and 5 haplotypes correlated with coronary atherosclerosis even after adjustment by Gensini score. At follow-up (median 53 months, range 1–60 months), 85 patients experienced CVE. However, there was no strong association between the gene polymorphisms and the occurrence of CVE. Tissue factor pathway inhibitor-2 gene polymorphisms were associated with coronary atherosclerosis in the Chinese population, suggesting that the information about TFPI-2 gene polymorphisms was useful for assessing the risk of developing coronary atherosclerosis, but there was not enough evidence showing it could predict occurrence of CVE.
机译:组织因子途径抑制剂-2(TFPI-2)可能在动脉粥样硬化的发病机制中起重要作用。在这项研究中,我们旨在探讨TFPI-2基因多态性与冠状动脉粥样硬化之间的关联。在本研究中注册了四百七名冠状动脉粥样硬化和306名冠状动脉正常冠状动脉的患者。用聚合酶链反应直接测序方法检测九个单核苷酸多态性(SNPS)(RS3763473,RS59805398,RS5999573,RS59740167,RS4517,RS4264和RS4271)。 Gensini评分评估了冠状动脉粥样硬化的严重程度。基线调查后,冠状动脉粥样硬化的患者随访了心血管事件(CVES)的发生率。八个SNP符合Hardy-Weinberg平衡,并且在连接不平衡和单倍型分析后,根据RS5999573,RS59740167和RS34489123构建了8个单倍型。两个SNP(RS59805398和RS34489123)和5个单倍型与冠状动脉粥样硬化相关,即使在Gensini得分调整后也是如此。随访(中位53个月,1-60个月的范围),85名患者经历过CVE。然而,基因多态性与CVE的发生之间没有强烈关联。组织因子途径抑制剂-2基因多态性与中国人口中的冠状动脉粥样硬化有关,表明TFPI-2基因多态性的信息可用于评估冠状动脉粥样硬化的风险,但没有足够的证据表明它可以预测发生CVE。

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