载脂蛋白e基因多态性是缺血性脑血管病的危险因素

S. Stankovic, Zagorka Jovanovic-Markovic, N. Majkić-Singh, D. Stankovic, S. Glišić, D. Zivkovic, S. Kostic, N. D. Alavantic
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引用次数: 7

摘要

摘要:载脂蛋白E (apoE) DNA多态性与缺血性脑血管病的可能关联在65例中风或短暂性脑缺血发作患者和330名健康对照中进行了评估。通过限制性同型/MADGE分析确定ApoE基因型。病例组与对照组apoE基因型频率差异有统计学意义(p<0.01)。缺血性脑卒中患者E4等位基因频率高于同龄对照组,E2等位基因频率低于同龄对照组。与没有E4等位基因的人相比,携带E4等位基因的人发生中风的风险高出2.1倍。提示载脂蛋白e基因多态性可能是塞尔维亚人群发生缺血性脑血管病的危险因素。
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 gene polymorphism as a risk factor for ischemic cerebrovascular disease
Summary: The possible association of apolipoprotein E (apoE) DNA polymorphism with ischemic cerebrovascular disease was evaluated in 65 patients who had suffered completed stroke or transient ischemic attack and 330 healthy controls. ApoE genotypes were determined by restriction isotyping/MADGE analysis. Significant difference in apoE genotype frequencies between case and control group was observed (p<0.01). Patients affected by ischemic stroke had higher frequency of E4 allele and lower E2 allele than age-matched control subjects. Compared with persons without E4 allele, carriers of an E4 allele had 2.1 times higher risk of incident stroke. Our results indicate that the apoE gene polymorphism may be a risk factor for the development of ischemic cerebrovascular disease in Serbian population..
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