Epigenetics in allergic diseases

被引:27
作者
DeVries, Avery [1 ,2 ]
Vercelli, Donata [2 ,3 ,4 ,5 ]
机构
[1] Univ Arizona, Grad Program Cellular & Mol Med, Tucson, AZ USA
[2] Univ Arizona, Arizona Resp Ctr, Funct Genom Lab, Tucson, AZ USA
[3] Univ Arizona, Arizona Ctr Biol Complex Dis, Tucson, AZ USA
[4] Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ USA
[5] Univ Arizona, Inst Bio5, Tucson, AZ USA
关键词
allergic disease; DNA methylation; epigenetics; DNA METHYLATION; CHILDHOOD ASTHMA; EARLY-LIFE; CHILDREN; EXPOSURE; GENETICS; RISK;
D O I
10.1097/MOP.0000000000000285
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose of reviewAllergic 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.Recent findingsDifferential DNA methylation at specific regions appears to be associated with concurrent allergic disease. A few studies have identified methylation signatures predictive of disease.SummaryDNA 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.
引用
收藏
页码:719 / 723
页数:5
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