中国北方汉族人群载脂蛋白B基因多态性与原发性高血压的关系

Wei-Yan Zhao, Jian-Feng Huang, Lai-Yuan Wang, Hong-Fan Li, Peng-Hua Zhang, Qi Zhao, Shu-Feng Chen, Dong-Feng Gu
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摘要

目的:探讨华北汉族人群载脂蛋白B基因多态性与原发性高血压的关系。方法:采用聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)方法对503例无亲缘关系高血压患者和490名健康对照进行载脂蛋白B (APOB)基因XbaI和EcoRI多态性分型。结果:组间基因型分布的差异可以忽略不计。健康对照中X+等位基因的检出率(4.8%)低于中国人,病例中X+等位基因的检出率(5.7%)与对照组无显著差异(P = 0.38)。观察到的E-等位基因频率在组间非常相似(病例5.9% vs对照组5.0%,P = 0.39)。logistic回归分析显示,在调整了其他环境因素后,这种相关性仍然存在。单倍型分析显示,X-E+是最常见的,没有单倍型与原发性高血压有显著关系。结论:APOB基因XbaI和EcoRI多态性与中国北方汉族人群原发性高血压无关。未来需要对更大样本的单核苷酸多态性进行研究,以进一步研究APOB基因对原发性高血压的可能贡献。
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Association of the apolipoprotein B gene polymorphisms with essential hypertension in Northern Chinese Han population.

Objective: To study the association of the apolipoprotein B gene polymorphisms with essential hypertension in Northern Chinese Han population.

Methods: XbaI and EcoRI polymorphisms of the apolipoprotein B (APOB) gene were genotyped by polymerase chain reaction (PCR) and restriction fragment-length polymorphism (RFLP) method in 503 unrelated hypertensive patients and 490 healthy controls recruited from international collaborative study of cardiovascular disease in Asia (InterAsia).

Results: The difference in the genotypic distributions could be neglected across the groups. The prevalence of X+ allele in healthy controls (4.8%) was less frequent in Chinese, and there was no significant difference in the frequency of the X+ allele between cases (5.7%) and controls (P = 0.38). The observed E- allele frequencies were closely similar among groups (5.9% in cases vs 5.0% in controls, P = 0.39). Logitstic regression analyses revealed that the lack of association still persisted after adjustment of other environmental factors. Haplotype analysis showed that X-E+ was most frequent and no haplotype could significantly contribute to essential hypertension.

Conclusion: The APOB gene XbaI and EcoRI polymorphisms are not associated with essential hypertension in the Northern Chinese Han population. Future studies on single nucleotide polymorphisms in larger samples are needed to further investigate the possible contribution of the APOB gene to essential hypertension.

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