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Correlation between peripheral blood Cx40 gene polymorphism and atherosclerotic plaque property development in patients with cerebral infarction

机译:脑梗死患者外周血Cx40基因多态性与动脉粥样硬化斑块性质发展的相关性

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Objective: To study the correlation between peripheral blood connexin 40 (Cx40) gene polymorphism and atherosclerotic plaque property development in patients with cerebral infarction. Methods: Patients who were treated in the Second Affiliated Hospital of Xi'an Medical University due to acute cerebral infarction between March 2015 and March 2018 were selected as cerebral infarction group, and healthy subjects who received physical examination during the same period were selected as control group. Peripheral blood was collected to detect the polymorphism of Cx40 gene rs35594137 locus, and serum was collected to determine the contents of cytokines, proteases and related molecules. Results: The constituent ratio of Cx40 gene AA+AG genotype in peripheral blood of cerebral infarction group was higher than that of control group whereas the constituent ratio of GG genotype was lower than that of control group; serum IL-17, HMGB1, VCAM1, MCP-1, P-selectin, YKL-40, MMP9, TIMP1 and Caspase-3 contents as well as MMP9/TIMP1 ratio of cerebral infarction group were significantly higher than those of control group whereas ADAMTS13 and Vaspin contents were significantly lower than those of control group; serum IL-17, HMGB1, VCAM1, MCP-1, P-selectin, YKL-40, MMP9, TIMP1 and Caspase-3 contents as well as MMP9/TIMP1 ratio of cerebral infarction group of patients with CX40 gene AA+AG genotype were significantly higher than those of patients with GG genotype whereas ADAMTS13 and Vaspin contents were significantly lower than those of patients with GG genotype. Conclusion: The mutation from Cx40 gene rs35594137 allele G to A in peripheral blood of patients with cerebral infarction can promote the development of atherosclerotic plaque properties.
机译:目的:研究脑梗死患者外周血连接蛋白40(Cx40)基因多态性与动脉粥样硬化斑块性质发展的相关性。方法:选择2015年3月至2018年3月在西安医科大学第二附属医院接受治疗的急性脑梗死患者作为脑梗死组,并选择同期接受身体检查的健康受试者作为对照组。组。收集外周血以检测Cx40基因rs35594137基因座的多态性,并收集血清以确定细胞因子,蛋白酶和相关分子的含量。结果:脑梗死组外周血Cx40基因AA + AG基因型的构成比例高于对照组,而GG基因型的构成比例低于对照组。脑梗死组血清IL-17,HMGB1,VCAM1,MCP-1,P-选择素,YKL-40,MMP9,TIMP1和Caspase-3的含量以及MMP9 / TIMP1比值明显高于对照组,而ADAMTS13 Vaspin含量明显低于对照组。 CX40基因AA + AG基因型患者脑梗死组的血清IL-17,HMGB1,VCAM1,MCP-1,P-选择素,YKL-40,MMP9,TIMP1和Caspase-3含量以及MMP9 / TIMP1比值显着高于GG基因型患者,而ADAMTS13和Vaspin含量显着低于GG基因型患者。结论:脑梗死患者外周血Cx40基因rs35594137等位基因G突变为A可促进动脉粥样硬化斑块特性的发展。

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