中度至重度哮喘全基因组关联研究的观点和简要概述

M. Hoque
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引用次数: 0

摘要

哮喘是一种常见的慢性呼吸系统疾病,具有表型遗传性,在亲属中表现为症状聚集性。在过去的三十年里,人们进行了大量的研究来检查哮喘的遗传易感性。在过去的十年中,全基因组关联研究(GWAS)重新审视了哮喘的观点,并确定了一些与哮喘易感性相关的新基因。然而,针对中重度哮喘的遗传学研究很少,分子靶点解释了哮喘遗传力的一小部分。这篇综述的重点是研究中度至重度哮喘全基因组关联的基因组研究的主要发现,以及它是如何将基于表型的方法过渡到基础基因组研究的。它进一步说明了旨在翻译精准医学研究结果的综合观点。因此,更好地了解哮喘发病机制将使个体成为哮喘护理的中心。易卜拉欣·迈德,上校。j . 2021;15 (2): 52 - 61
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perspective and a brief overview of genome-wide association studies in moderate to severe asthma
Asthma is a common chronic respiratory disease that shares phenotypic heritability and shows clusters of symptoms among the relatives. A large number of studies have been conducted to examine the genetic susceptibility of asthma over the past three decades. In the last decade, genome-wide association studies (GWAS) have readdressed the perspective of viewing asthma and have identified some novel genes associated with the susceptibility of asthma. However, few genetic studies have been conducted focusing the moderate to severe asthma, and the molecular targets explain a small proportion of asthma heritability. This review focuses on the principal findings of the genomic studies investigating the genome-wide association of moderate to severe asthma and how it is transitioning the phenotype-based approach towards the fundamental genomic studies. It further illustrates the integrative perspectives aimed towards the translation of the findings in precision medicine. Therefore, a better understanding of asthma pathogenesis would focus the individual at the center of asthma care. Ibrahim Med. Coll. J. 2021; 15(2): 52-61
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