SNP及其与高血压的相关性:一项综合综述

M. Murugan, K. Ramalingam, M. Nazzuredin, Hussain Ahmed Rashed, Ganesh Punamalai
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引用次数: 3

摘要

高血压是一个日益严重的全球性问题,主要影响成年人。它是中风、心肌梗死、充血性心力衰竭、缺血性心脏病、周围血管疾病和进行性肾损害死亡的危险因素。这些疾病造成相当高的发病率和高死亡率。人类原发性高血压(EH)是一种复杂的多因素特征,受环境和遗传因素的影响。早期发现高血压患者的遗传易感性将有助于及时治疗和避免并发症。最近在人类基因组中发现了400多万个snp,这些snp有可能成为建立遗传联系和作为疾病指标的遗传标记的丰富来源,从而促进了snp在遗传病检测中的使用。这样的基因研究将为高血压等疾病的诊断和治疗开辟新的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SNP′s and its correlation with hypertension: A comprehensive review
Hypertension is a growing global problem, which mostly affects the adults. It is a risk factor for death from stroke, myocardial infarction, congestive heart failure, ischemic heart disease, peripheral vascular disease, and progressive renal damage. These diseases are responsible for considerable morbidity and high mortality rate. Human essential hypertension (EH) is a complex and multifactorial trait influenced by environmental and genetic determinants. Early detection of genetic predisposition in hypertensive patients will enable prompt treatment and avoidance of complications. The use of SNPs in genetic disease detection is facilitated by the recent discovery of more than 4 million SNPs in the human genome that have the potential to be a rich source of genetic markers to establish genetic linkage and as indicators of disease. Such genetic research will open the new frontiers in diagnosis and treatment of diseases like hypertension.
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