表观基因组
暴露的
疾病
炎症性肠病
微生物群
全基因组关联研究
遗传力
表观遗传学
生物
基因组学
遗传力缺失问题
表观遗传学
遗传学
生物信息学
基因组
医学
DNA甲基化
基因
单核苷酸多态性
病理
基因表达
基因型
作者
Alexandra Noble,Jan Krzysztof Nowak,Alex Adams,Holm H. Uhlig,Jack Satsangi
标识
DOI:10.1053/j.gastro.2023.03.238
摘要
Recent advances in our understanding of the pathogenesis of inflammatory bowel disease (IBD) have highlighted the complex interplay between the genome, the epigenome, and the environment. Despite the exciting advances in genomics that have enabled the identification of over 200 susceptibility loci, these only account for a small proportion of the disease variance and the estimated heritability in IBD. It is likely that gene-environment (GxE) interactions contribute to "missing heritability" and these may act through epigenetic mechanisms. Several environmental factors, such as the microbiome, nutrition, and tobacco smoking, induce alterations in the epigenome of children and adults, which may impact disease susceptibility. Other mechanisms for GxE interactions are also directly pertinent in early life. We discuss a model in which environmental factors imprint disease risk in a window of susceptibility during infancy that may contribute to later disease onset, whereas other elements of the exposome act later in life and contribute directly to the pathogenesis and course of the disease. Understanding the mechanisms underlying GxE interactions may provide the basis for new therapeutic targets or preventative strategies for IBD.
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