表观遗传学
生物
孟德尔随机化
全基因组关联研究
DNA甲基化
遗传学
背景(考古学)
遗传关联
计算生物学
表达数量性状基因座
组蛋白
后生
基因组学
生物信息学
遗传倾向
人类遗传学
基因
表观遗传学
进化生物学
候选基因
孟德尔遗传
单核苷酸多态性
疾病
生物途径
遗传变异
转录组
数量性状位点
维生素D与神经学
主要组织相容性复合体
机制(生物学)
基因表达调控
作者
Benjamin M Jacobs,Marijne Vandebergh,Vicki E. Maltby,Ruth Dobson,Karim L Kreft
出处
期刊:Brain
[Oxford University Press]
日期:2026-03-26
标识
DOI:10.1093/brain/awag111
摘要
Genome-wide association studies (GWAS) have identified over 230 genetic variants associated with susceptibility to multiple sclerosis (MS) and one genome-wide significant variant associated with progression of MS. Environmental risk factors, such as vitamin D deficiency and obesity, have also been implicated in MS pathogenesis. Statistical approaches building on these genetic data, such as Mendelian randomization and colocalization, have established putative causal links between environmental risk factors and MS risk, most notably for vitamin D and body mass index. However, studies have thus far revealed limited statistically significant interactions between host genetics and environmental factors beyond the Major Histocompatibility Complex. Epigenetics - the study of non-nucleotide alterations to DNA such as DNA methylation or histone acetylation - might provide a mechanistic framework for understanding how environmental and genetic factors interact in MS. Environmental factors, such as Epstein-Barr virus (EBV) infection, vitamin D deficiency, and smoking, are associated with epigenetic modifications at key MS-related genomic loci, altering the expression of MS risk genes in a cell-type specific manner. Transcriptomics have identified significant pathways via which genetic risk is realised, potentially providing targets for intervention. This review synthesizes current evidence on gene-environment interactions in the context of MS GWAS findings, evaluates the strengths and limitations of various study methodologies, and discusses the challenges in elucidating the interplay between genetics and environmental factors. We propose potential strategies for future research to advance our understanding of the biological mechanisms underlying MS susceptibility in at-risk individuals.
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