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

被引:0
|
作者
Gholamalizadeh, Hanieh [1 ,2 ]
Amiri-Shahri, Maedeh [3 ,4 ]
Rasouli, Fatemeh [3 ,4 ]
Ansari, Arina [3 ,4 ]
Baradaran Rahimi, Vafa [5 ]
Reza Askari, Vahid [6 ]
机构
[1] Mashhad Univ Med Sci, Student Res Comm, Mashhad 1313199137, Iran
[2] Mashhad Univ Med Sci, Fac Med, Mashhad 9177948564, Iran
[3] North Khorasan Univ Med Sci, Student Res Comm, Bojnurd 9414975516, Iran
[4] North Khorasan Univ Med Sci, Fac Med, Bojnurd 9414975516, Iran
[5] Mashhad Univ Med Sci, Fac Med, Dept Cardiovasc Dis, Mashhad 9177948564, Iran
[6] Mashhad Univ Med Sci, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
关键词
autism spectrum disorders; DNA methylation; epigenetics; animal model; biomarkers; OXYTOCIN RECEPTOR GENE; FAMILY-BASED ASSOCIATION; VALPROIC ACID; MECP2; BRAIN; DYSREGULATION; DOPAMINE; MODEL; CPG; IDENTIFICATION;
D O I
10.3390/brainsci14080737
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
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页数:23
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