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Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability

机译:Adams7多态性与颈动脉arty斑块漏洞之间的关联

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Recent genome-wide association studies (GWAS) indicated that polymorphisms in ADAMTS7 were associated with artery disease caused by atherosclerosis . However, the correlation between the ADAMTS7 polymorphism and plaque stability remains unclear. The objective of this study was to evaluate the association between 2 ADAMTS7 variants rs3825807 and rs7173743 and ischemic stroke or atherosclerotic plaque vulnerability. This research is an observational study. Patients with ischemic stroke and normal control individuals admitted to Beijing Tiantan Hospital from May 2014 to October 2017 were enrolled. High-resolution magnetic resonance imaging was used to distinguish vulnerable and stable carotid plaques. The ADAMTS7 SNPs were genotyped using TaqMan assays on real-time PCR system. The multivariate logistic regression analyses were used to adjust for multiple risk factors between groups. Three hundred twenty-six patients with ischemic stroke (189 patients with vulnerable plaque and 81 patients with stable plaque) and 432 normal controls were included. ADAMTS7 polymorphisms of both rs7173743 and rs3825807 were associated with carotid plaque vulnerability but not the prevalence of ischemic stroke. The T/T genotype of rs7173743 [odds ratio (OR) = 1.885, 95% confidence interval (CI) = 1.067–3.328, P = .028] and A/A genotype of rs3825807 (OR = 2.146, 95% CI = 1.163–3.961, P = .013) were considered as risk genotypes for vulnerable plaque susceptibility. In conclusion, ADAMTS7 variants rs3825807 and rs7173743 are associated with the risk for carotid plaque vulnerability.
机译:最近的基因组 - 宽协会研究(GWAS)表明,Adamts7中的多态性与由动脉粥样硬化引起的动脉疾病有关。然而,Adamts7多态性与斑块稳定性之间的相关性仍不清楚。本研究的目的是评估2个Adamts7变体RS3825807和RS7173743和缺血性卒中或动脉粥样硬化斑块脆弱性的关联。该研究是一个观察性研究。患有缺血性卒中和北京天坛医院的患者于2014年5月至2017年10月入学。高分辨率磁共振成像用于区分脆弱且稳定的颈动脉斑块。使用Taqman测定在实时PCR系统上进行基因分型进行基因分型。多变量逻辑回归分析用于调整组之间的多种风险因素。包括三百二十六名缺血性卒中患者(189例脆弱斑块患者和81例稳定斑块患者)和432例正常对照。 rs7173743和rs3825807的Adamts7多态性与颈动脉斑块脆弱性有关,但不是缺血性卒中的患病率。 RS7173743的T / T基因型[差距(或)= 1.885,95%置信区间(CI)= 1.067-3.328,P = .028]和RS3825807的A / A基因型(或= 2.146,95%CI = 1.163 -3.961,p = .013)被认为是脆弱斑块易感性的风险基因型。总之,Adamts7变体RS3825807和RS7173743与颈动脉斑块脆弱性的风险有关。

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