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自闭症谱系障碍中的DNA甲基化:生物标志物还是药理学靶点?

DNA Methylation in Autism Spectrum Disorders: Biomarker or Pharmacological Target?

作者信息

Gholamalizadeh Hanieh, Amiri-Shahri Maedeh, Rasouli Fatemeh, Ansari Arina, Baradaran Rahimi Vafa, Reza Askari Vahid

机构信息

Student Research Committee, Mashhad University of Medical Sciences, Mashhad 13131-99137, Iran.

Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 91779-48564, Iran.

出版信息

Brain Sci. 2024 Jul 23;14(8):737. doi: 10.3390/brainsci14080737.

Abstract

Autism spectrum disorder (ASD) is a group of heterogeneous neurodevelopmental disabilities with persistent impairments in cognition, communication, and social behavior. Although environmental factors play a role in ASD etiopathogenesis, a growing body of evidence indicates that ASD is highly inherited. In the last two decades, the dramatic rise in the prevalence of ASD has interested researchers to explore the etiologic role of epigenetic marking and incredibly abnormal DNA methylation. This review aimed to explain the current understanding of the association between changes in DNA methylation signatures and ASD in patients or animal models. We reviewed studies reporting alterations in DNA methylation at specific genes as well as epigenome-wide association studies (EWASs). Finally, we hypothesized that specific changes in DNA methylation patterns could be considered a potential biomarker for ASD diagnosis and prognosis and even a target for pharmacological intervention.

摘要

自闭症谱系障碍(ASD)是一组异质性神经发育障碍,在认知、沟通和社交行为方面存在持续性损伤。尽管环境因素在ASD的病因发病机制中起作用,但越来越多的证据表明ASD具有高度遗传性。在过去二十年中,ASD患病率的急剧上升促使研究人员探索表观遗传标记和极其异常的DNA甲基化的病因学作用。本综述旨在解释目前对患者或动物模型中DNA甲基化特征变化与ASD之间关联的理解。我们回顾了报告特定基因DNA甲基化改变的研究以及全表观基因组关联研究(EWAS)。最后,我们推测DNA甲基化模式的特定变化可被视为ASD诊断和预后的潜在生物标志物,甚至是药物干预的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d75/11352561/0607beba78f8/brainsci-14-00737-g001.jpg

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