DeVries Avery, Vercelli Donata
aGraduate Program in Cellular and Molecular Medicine bFunctional Genomics Laboratory, Arizona Respiratory Center cArizona Center for the Biology of Complex Diseases dDepartment of Cellular and Molecular Medicine eThe Bio5 Institute, University of Arizona, Tucson, Arizona, USA.
Curr Opin Pediatr. 2015 Dec;27(6):719-23. doi: 10.1097/MOP.0000000000000285.
Allergic diseases are among the most prevalent chronic diseases of childhood, affecting more than 7 million children in the United States. Epidemiological evidence supports the idea that the inception of allergic diseases is typically before the preschool years, even when chronic symptoms do not emerge until adulthood. The role of epigenetic mechanisms (particularly DNA methylation) in allergic disease is under active investigation because these mechanisms are known to be at the interface of gene regulation, environmental stimuli, and developmental processes, all of which are essential for the pathogenesis for asthma and allergy. This article specifically reviews genome-wide DNA methylation studies in allergic disease.
Differential DNA methylation at specific regions appears to be associated with concurrent allergic disease. A few studies have identified methylation signatures predictive of disease.
DNA methylation signatures have been shown to be associated with several allergic disease phenotypes, typically concurrently with disease. The few that have been found to precede diagnosis are especially interesting because they highlight an early trajectory to disease.
过敏性疾病是儿童期最常见的慢性疾病之一,在美国影响着超过700万儿童。流行病学证据支持这样一种观点,即过敏性疾病通常在学龄前就已开始,即使慢性症状直到成年才出现。表观遗传机制(尤其是DNA甲基化)在过敏性疾病中的作用正在积极研究中,因为这些机制已知处于基因调控、环境刺激和发育过程的交汇点,而所有这些对于哮喘和过敏的发病机制都是必不可少的。本文特别综述了过敏性疾病的全基因组DNA甲基化研究。
特定区域的DNA甲基化差异似乎与同时发生的过敏性疾病有关。一些研究已经确定了可预测疾病的甲基化特征。
DNA甲基化特征已被证明与几种过敏性疾病表型有关,通常与疾病同时出现。少数在诊断前就已发现的特征尤其有趣,因为它们突出了疾病的早期发展轨迹。