食物过敏的遗传危险因素:全基因组研究综述

U. V. Konovalova, O. Fedorova, E. Bragina
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引用次数: 0

摘要

的相关性。食物过敏(FA)是全世界公共卫生面临的一个紧迫问题:这种疾病降低了患者的生活质量,增加了发生不可预测的过敏反应的风险。材料和方法。为了研究遗传因素对FA发生的影响,对全基因组关联研究结果进行了分析。本次评审包括2012年1月1日至2021年12月31日期间发表的原创文章。在FA患者队列中进行遗传研究分析,旨在评估遗传因素在该病理发展中的作用。结果。本文综述了与FA相关的遗传变异关系的系统数据。通过对8项研究的分析,发现欧洲人SLC2A9基因的rs10018666变体在ige介导的FA发育过程中对花生的影响最大。一些与特定基因座相关的过敏原已被发现,如变异rs9273440 (HLA-DQB1)、rs115218289 (ITGA6)、rs10018666 (SLC2A9)等是花生所特有的。相关变异主要与先天/适应性免疫反应和上皮屏障功能紊乱有关,证实了它们在FA发展中的主导作用。除了与FA相关外,大多数已确定的基因还影响其他“过敏性进行”表型的发展,包括特应性皮炎、支气管哮喘、变应性鼻炎以及非过敏性(2型糖尿病、帕金森病、心肌梗死等)疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic risk factors of food allergy: a review of genome-wide studies
Relevance. Food allergy (FA) is an urgent problem for public health around the world: this disease reduces the quality of life of patients, increases the risk of developing unpredictable anaphylactic reactions. Materials and methods. An analysis was made of the results of genome-wide association studies aimed at studying the influence of genetic factors in the development of FA. The review includes original articles published for the period from January 1, 2012 to December 31, 2021 Target. Conduct an analysis of genetic studies in cohorts of patients with FA aimed at assessing the role of genetic factors in the development of this pathology. Results. This review systematize data on the relationship of genetic variations associated with FA. Eight studies were analyzed, the maximum effect with the development of IgE-mediated FA on peanuts was found for the rs10018666 variant of the SLC2A9 gene in Europeans. Some allergens, associations with specific loci have been found, for example, variants rs9273440 (HLA-DQB1), rs115218289 (ITGA6), rs10018666 (SLC2A9) and others are unique to peanut. Associated variants are predominantly associated with disorders of the innate/adaptive immune response and the functioning of the epithelial barrier, confirming their leading role in the development of FA. In addition to associations with FA, most of the identified genes affect the development of other "allergic march" phenotypes, including atopic dermatitis, bronchial asthma, allergic rhinitis, as well as non-allergic (type 2 diabetes mellitus, Parkinson's disease, myocardial infarction, and others) diseases.
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