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Association of LOX-1 gene polymorphisms with cerebral infarction in northern Chinese Han population

机译:中国北方汉族人群LOX-1基因多态性与脑梗死的关系

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摘要

Background Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) plays an important role in the pathophysiology of atherosclerosis and thrombosis. This study is aimed at evaluating the potential association of 3’-UTR-C188T and G501C in LOX-1 gene with cerebral infarction. Methods A total of 386 patients with cerebral infarction and 386 healthy controls were included in the study, which were unrelated Chinese Han population in the Liaoning Province of northern China. The single nucleotide polymorphisms, 3’-UTR-C188T and G501C, were analyzed by polymerase chain reaction–ligation detection reaction method. Results The frequencies of CC?+?GC genotype, GC genotype and C allele of G501C in the patients with cerebral infarction were significantly higher than those in the controls (P?
机译:背景凝集素样氧化型低密度脂蛋白受体1(LOX-1)在动脉粥样硬化和血栓形成的病理生理中起重要作用。这项研究旨在评估LOX-1基因中的3'-UTR-C188T和G501C与脑梗死的潜在关联。方法将386名脑梗死患者和386名健康对照纳入研究对象,这些患者与中国北方辽宁省的汉族人群无关。通过聚合酶链反应-连接检测反应方法分析了3'-UTR-C188T和G501C的单核苷酸多态性。结果脑梗死患者G501C的CCα+ΔGC基因型,GC基因型和C等位基因频率明显高于正常对照组(P <0.01,P <0.01,P = 0.04)。 , 分别)。在调整了脑梗死的危险因素后,相关性仍然存在。此外,在3'-UTR-C188T与脑梗死之间未发现显着关联。结论研究表明,LOX-1基因的G501C变异可能与中国北方汉族人群的脑梗死易感性有关,而与其他常见危险因素无关。

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