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遗传风险与儿童期起病哮喘。

Genetic risks and childhood-onset asthma.

机构信息

Division of Respiratory Science, Imperial College London, London, United Kingdom.

出版信息

J Allergy Clin Immunol. 2011 Aug;128(2):266-70; quiz 271-2. doi: 10.1016/j.jaci.2011.06.026.

Abstract

Recent large-scale genome-wide association studies have successfully identified several genetic loci that influence asthma susceptibility. The loci thus far identified confer a high population attributable risk for childhood-onset disease and have provided a better understanding of the primary mechanisms underlying asthma and a clear focus for new therapies to treat the disease. The loci are of limited utility for diagnostic or predictive genetic testing. This review considers different aspects of genetic risk, including individual, population, and familial risks, and explores how these different measures interact and how the next generation of genetic studies might be best designed.

摘要

最近的大规模全基因组关联研究成功地确定了几个影响哮喘易感性的遗传位点。迄今为止,这些发现的遗传位点为儿童发病的疾病提供了高人群归因风险,并为哮喘的主要机制提供了更好的理解,并为治疗该疾病的新疗法提供了明确的重点。这些遗传位点在诊断或预测性基因检测方面的作用有限。本综述考虑了遗传风险的不同方面,包括个体、人群和家族风险,并探讨了这些不同的措施如何相互作用,以及下一代遗传研究可能如何最好地设计。

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