Structural, Functional, and Molecular Imaging of Autism Spectrum Disorder

被引:0
|
作者
Xiaoyi Li
Kai Zhang
Xiao He
Jinyun Zhou
Chentao Jin
Lesang Shen
Yuanxue Gao
Mei Tian
Hong Zhang
机构
[1] The Second Hospital of Zhejiang University School of Medicine,Department of Nuclear Medicine and Medical PET Center
[2] Key Laboratory of Medical Molecular Imaging of Zhejiang Province,Key Laboratory for Biomedical Engineering of Ministry of Education
[3] Zhejiang University,Laboratory for Pathophysiological and Health Science
[4] RIKEN Center for Biosystems Dynamics Research,Department of Surgical Oncology
[5] The Second Hospital of Zhejiang University School of Medicine,Institute of Nuclear Medicine and Molecular Imaging
[6] Zhejiang University,undefined
[7] The College of Biomedical Engineering and Instrument Science of Zhejiang University,undefined
来源
Neuroscience Bulletin | 2021年 / 37卷
关键词
Autism spectrum disorder; Positron emission tomography; Magnetic resonance imaging; Molecular imaging; Functional connectivity; Serotonin; Oxytocin;
D O I
暂无
中图分类号
学科分类号
摘要
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder associated with both genetic and environmental risks. Neuroimaging approaches have been widely employed to parse the neurophysiological mechanisms underlying ASD, and provide critical insights into the anatomical, functional, and neurochemical changes. We reviewed recent advances in neuroimaging studies that focused on ASD by using magnetic resonance imaging (MRI), positron emission tomography (PET), or single-positron emission tomography (SPECT). Longitudinal structural MRI has delineated an abnormal developmental trajectory of ASD that is associated with cascading neurobiological processes, and functional MRI has pointed to disrupted functional neural networks. Meanwhile, PET and SPECT imaging have revealed that metabolic and neurotransmitter abnormalities may contribute to shaping the aberrant neural circuits of ASD. Future large-scale, multi-center, multimodal investigations are essential to elucidate the neurophysiological underpinnings of ASD, and facilitate the development of novel diagnostic biomarkers and better-targeted therapy.
引用
收藏
页码:1051 / 1071
页数:20
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