新疆哈萨克族、汉族心房颤动血栓栓塞与PS基因多态性及可溶性P-选择素相关性研究
投稿时间:2014-10-19  修订日期:2014-11-28  点此下载全文
引用本文:古丽米拉·米尔扎,刘志强,马尔加恩·巴克依,木胡牙提·乌拉斯汉.新疆哈萨克族、汉族心房颤动血栓栓塞与PS基因多态性及可溶性P-选择素相关性研究[J].医学研究杂志,2015,44(4):32-36
DOI: 10.11969/j.issn.1673-548X.2015.04.010
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作者单位E-mail
古丽米拉·米尔扎 830054 乌鲁木齐, 新疆医科大学第一附属医院心脏中心  
刘志强 830054 乌鲁木齐, 新疆医科大学第一附属医院心脏中心 2556295331@qq.com 
马尔加恩·巴克依 830054 乌鲁木齐, 新疆医科大学第一附属医院心脏中心  
木胡牙提·乌拉斯汉 830054 乌鲁木齐, 新疆医科大学第一附属医院心脏中心 muhuyati@163.com 
基金项目:国家自然科学基金资助项目(81260036)
中文摘要:目的 研究新疆维吾尔自治区哈萨克族、汉族心房颤动(以下简称房颤)合并血栓栓塞P-选择素(P-selectin,PS)基因在2123C/G、Thr715Pro位点多态性与可溶性P-选择素(souble P-selectin,sPs)血浆水平的相关性。 方法 收集新疆维吾尔自治区哈萨克族248例(其中病例组98例,对照组150例)、汉族340例(其中病例组121例,对照组219例),采用聚合酶链反应-限制性片段长度多态性法(PCR-RFLP)进行PS基因2123C/G、Thr715Pro位点多态性直接DNA序列分析,ELISA法测定血浆sPs水平。 结果 哈萨克族、汉族人群PS基因2123C/G位点基因型和等位基因频率分布差异无统计学意义(P=0.064,P=0.453),汉族、哈萨克族房颤合并血栓栓塞患者sPs血浆水平与房颤患者差异有统计学意义(P=0.000)。汉族、哈萨克族人群未检测出Thr715Pro基因多态性。 sPs血浆水平与2123C/G基因多态性有明显相关性,GG基因型的sPs水平显著高于CG+CC基因型(P<0.05)。 结论 PS基因多态性与血浆sPs水平或血栓栓塞事件相关,房颤患者并发血栓栓塞事件可能存在遗传易感性。
中文关键词:心房颤动  可溶性P-选择素  基因多态性
 
Association of PS Gene Polymorphism with Soluble P-selectin Levels and Atrial Fibrillation Thromboembolism in Kazaks and Hans of Xinjiang
Abstract:Objective To investigate the association of the 2123C/G and Thr715Pro polymorphisms of P selectin (PS) with plasma levels of soluble P-selectin in Han and Kazak patients with atrial fibrillation (AF) coupled with thrombosis in Xinjiang. Methods Totally 248 age-and sex-matched Kazak subjects (150 control subjects and 98 AF patients) and 340 Han subjects (219 control subjects and 121 AF patients) were enrolled. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and direct DNA sequence analysis were used to investigate 2123C/G and Thr715Pro polymorphisms. ELISA method was used to determine plasma levels of SPs. Results Plasma sPS levels showed significant difference between Han and Kazak case and control groups (P=0.000). The frequency distribution of the 2123C/G and the allele showed no significant differences between Kazak and Han population (P=0.064,P=0.453). Thr715Pro did not show any polymorphism in the two populations. Plasma sPS levels were significantly associated with the 2123C/G polymorphism, and signifiacntly higher in the patients with GG genotype than in those with GC or CC genotype (P<0.05). Conclusion PS gene polymorphisms are associated with plasma levels of sP-selectin, suggesting that the patients with nonvalvular AF and thromboembolic events may have genetic susceptibility.
keywords:Atrial fibrillation  Soluble P-selectin  Gene polymorphism
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