钙化性主动脉瓣狭窄老年患者的载脂蛋白 E 多态性与血脂异常

Erum Afaq, Muhammad Kashif Nisar, Asif Iqbal Khan, Mamoona Shafiq, Muhammad Irfan ul Akbar Yousufzai, Saeed Khan
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引用次数: 0

摘要

研究目的本研究旨在调查载脂蛋白 E 多态性对血浆脂质谱的影响,并确定载脂蛋白 E 基因多态性是巴基斯坦人群钙化性 AS 的遗传预测因子。 研究方法:这是一项在卡拉奇陶尔健康科学大学和国家心血管疾病研究所进行的病例对照研究。研究共包括 100 人,其中 50 人为超声心动图确定的钙化性 AS 病例,50 人为年龄和性别匹配的对照组。通过聚合酶链式反应(PCR)和限制性片段长度多态性(RFLP)技术,计算了载脂蛋白 E 等位基因频率,估计了血脂概况,并确定了载脂蛋白 E 基因多态性。 研究结果钙化性强直性脊柱炎病例中载脂蛋白E 2、3和4等位基因频率分别为16%、52%和32%,对照组分别为10%、52%和28%(P=0.622)。在50个病例中,18%为轻度强直性脊柱炎,22%为中度强直性脊柱炎,60%为重度钙化性强直性脊柱炎。据观察,在病例和对照组中,载脂蛋白 E4 等位基因的总胆固醇(TC)、甘油三酯(TG)和低密度脂蛋白(LDL)水平均高于其他基因。 结论本研究结果表明,载脂蛋白 E 基因的载脂蛋白 E4 等位基因是血脂异常的一个不确定的危险因素,而载脂蛋白 E4 等位基因与钙化性强直性脊柱炎无关,这说明 CAD 和强直性脊柱炎的遗传背景各不相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apolipoprotein E Polymorphism And Dyslipidemia In Elderly Patients Of Calcific Aortic Stenosis
Objective: This study aimed to investigate the impact of the Apo E polymorphisms on plasma lipid profile and to identify the polymorphism of the apo-E gene as genetic predictor of calcific AS in Pakistani population.   Methodology: This was a case control study conducted in Dow University of Health Sciences and National Institute of Cardiovascular Disease, Karachi. It included total of 100 individuals, 50 echocardiographically identified calcific AS cases and 50 age and gender matched controls. Apo E allele frequencies were computed, lipid profiles were estimated and Apo E gene polymorphism was identified by the techniques of polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP).   Result: Apo E 2, 3, and 4 allele frequencies were 16%, 52%, and 32% in calcific AS cases, and 10%, 52%, 28% in controls respectively (p=0.622). Out of 50 cases, 18% presented with mild AS, 22% moderate AS and 60% lied in severe calcific AS. It was observed that levels of total cholesterol (TC), triglyceride (TG) and low-density lipoprotein (LDL) were higher in Apo E4 allele as compared to other genes in both cases and control.   Conclusion: The findings of this study suggested that Apo E4 allele of Apo E gene is an impotent risk factors for dyslipidemia while Apo E4 allele is not associated with calcific AS contemplates distinctive genetic backgrounds of CAD and AS.
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