Eating Disorders Continuum, Douglas Institute, Montreal, Canada.
Department of Psychiatry, McGill University, Montreal, Canada.
World J Biol Psychiatry. 2023 Mar;24(3):254-259. doi: 10.1080/15622975.2022.2089731. Epub 2022 Jun 27.
Recent studies have reported altered methylation levels at disorder-relevant DNA sites in people who are ill with Anorexia Nervosa (AN) compared to findings in people with no eating disorder (ED) or in whom AN has remitted. The preceding implies state-related influences upon gene expression in people with AN. This study further examined this notion.
We measured genome-wide DNA methylation in 145 women with active AN, 49 showing stable one-year remission of AN, and 64 with no ED.
Comparisons revealed 205 differentially methylated sites between active and no ED groups, and 162 differentially methylated sites between active and remitted groups ( < 0.01). Probes tended to map onto genes relevant to psychiatric, metabolic and immune functions. Notably, several of the genes identified here as being differentially methylated in people with AN (e.g. , , ) have figured in previous studies on AN. Effects also associated illness chronicity and lower BMI with more pronounced DNA methylation alterations, and remission of AN with normalisation of DNA methylation.
Findings corroborate earlier results suggesting reversible DNA methylation alterations in AN, and point to particular genes at which epigenetic mechanisms may act to shape AN phenomenology.
最近的研究报告称,与没有饮食失调(ED)或 AN 已缓解的人相比,患有神经性厌食症(AN)的患者在与疾病相关的 DNA 位点的甲基化水平发生了改变。这意味着 AN 患者的基因表达存在与状态相关的影响。本研究进一步探讨了这一观点。
我们测量了 145 名患有活动期 AN 的女性、49 名 AN 稳定缓解一年的女性和 64 名无 ED 的女性的全基因组 DNA 甲基化水平。
比较发现,活动期与无 ED 组之间有 205 个差异甲基化位点,活动期与缓解组之间有 162 个差异甲基化位点(<0.01)。探针倾向于映射到与精神、代谢和免疫功能相关的基因。值得注意的是,在这里被确定为 AN 患者中存在差异甲基化的几个基因(例如,、、)在以前的 AN 研究中出现过。此外,疾病的慢性和 BMI 的降低与更明显的 DNA 甲基化改变相关,AN 的缓解与 DNA 甲基化的正常化相关。
这些发现证实了早期的研究结果,表明 AN 中存在可逆的 DNA 甲基化改变,并指出了特定的基因,其中表观遗传机制可能对 AN 的表现形式产生影响。