湿疹基因研究的新见解

IF 0.8 4区 生物学 Q4 GENETICS & HEREDITY
Medizinische Genetik Pub Date : 2023-04-05 eCollection Date: 2023-04-01 DOI:10.1515/medgen-2023-2010
Ingo Marenholz, Aleix Arnau-Soler, Oscar Daniel Rosillo-Salazar, Young-Ae Lee
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引用次数: 0

摘要

全基因组关联研究(GWAS)为复杂过敏性疾病的遗传决定因素提供了基本的见解。湿疹有58个易感位点。蛋白质改变变异与湿疹在12个位点上具有全基因组意义。然而,大多数风险变异位于基因组的非编码调控区域。在免疫应答和上皮屏障功能通路中富集了优先的靶基因。有趣的是,在不同过敏性疾病的遗传结构中发现了很大的重叠,指出了湿疹、哮喘、花粉热和食物过敏的共同病理机制。在这里,我们回顾了GWAS对湿疹的最新发现,包括罕见变异和遗传异质性在不同种族人群中的作用。此外,我们提供的基因基础孟德尔疾病的湿疹性皮肤炎症的概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New insights from genetic studies of eczema.

Genome-wide association studies (GWAS) provided fundamental insight into the genetic determinants of complex allergic diseases. For eczema, 58 susceptibility loci were reported. Protein-changing variants were associated with eczema at genome-wide significance at 12 loci. The majority of risk variants were, however, located in non-coding, regulatory regions of the genome. Prioritized target genes were enriched in pathways of the immune response and of epithelial barrier function. Interestingly, a large overlap in the genetic architecture underlying different allergic diseases was identified pointing to common pathomechanisms for eczema, asthma, hay fever, and food allergy. Here, we review the most recent findings from GWAS for eczema including the role of rare variants and genetic heterogeneity in ethnically diverse populations. In addition, we provide an overview of genes underlying Mendelian disorders featuring eczematous skin inflammation.

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来源期刊
Medizinische Genetik
Medizinische Genetik Medicine-Genetics (clinical)
CiteScore
1.40
自引率
9.10%
发文量
48
审稿时长
>12 weeks
期刊介绍: medizinischegenetik is a scientific journal that is owned and published by the German Society of Human Genetics e.V. since 1989. The journal was founded by Prof. Jan Murken, München. Self-published until 2006, from 2007-2019 published at Springer Verlag and since 2020 at De Gruyter. medizinischegenetik serves education and training among colleagues, the interdisciplinary exchange of knowledge in all areas of human genetics in clinics, practice, research and teaching. Each issue of the quarterly journal deals with a focus that provides a comprehensive overview of current developments in specific clinical pictures, technical developments and therapeutic approaches. All reviews are written in English language. The journal thus creates a platform for the international exchange of knowledge and increased awareness of German research activities in the scientific community. In addition, medizinischegenetik contains information on activities in its own subject in the German-language section. This includes conference reports, association announcements, personnel matters, statements and guidelines. With health policy questions, historical retrospectives and comments on current developments, the profession takes a stand on human genetic issues in Germany, Austria and Switzerland.
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