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本文引用的文献

1
Metabolic pathology of autism in relation to redox metabolism.自闭症的代谢病理学与氧化还原代谢的关系
Biomark Med. 2014;8(3):321-30. doi: 10.2217/bmm.13.158.
2
Inflammatory mediators as biomarkers in brain disorders.炎症介质作为脑部疾病的生物标志物。
Inflammation. 2014 Jun;37(3):639-48. doi: 10.1007/s10753-013-9780-2.
3
Assessing bioenergetic compromise in autism spectrum disorder with 31P magnetic resonance spectroscopy: preliminary report.利用31P磁共振波谱评估自闭症谱系障碍中的生物能量代谢受损:初步报告。
J Child Neurol. 2014 Feb;29(2):187-93. doi: 10.1177/0883073813498466. Epub 2013 Oct 18.
4
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.从全外显子组序列数据中鉴定小型外显子 CNV 及其在自闭症谱系障碍中的应用。
Am J Hum Genet. 2013 Oct 3;93(4):607-19. doi: 10.1016/j.ajhg.2013.09.001.
5
Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism.自闭症患者前额皮质中线粒体 DNA 拷贝数的改变和电子传递链复合物及丙酮酸脱氢酶的活性。
Transl Psychiatry. 2013 Sep 3;3(9):e299. doi: 10.1038/tp.2013.68.
6
Atypical developmental patterns of brain chemistry in children with autism spectrum disorder.自闭症谱系障碍儿童大脑化学的非典型发育模式。
JAMA Psychiatry. 2013 Sep;70(9):964-74. doi: 10.1001/jamapsychiatry.2013.1388.
7
Impaired synthesis and antioxidant defense of glutathione in the cerebellum of autistic subjects: alterations in the activities and protein expression of glutathione-related enzymes.自闭症患者小脑中海藻糖-3-磷酸合成酶和抗氧化防御能力受损:谷胱甘肽相关酶的活性和蛋白表达改变。
Free Radic Biol Med. 2013 Dec;65:488-496. doi: 10.1016/j.freeradbiomed.2013.07.021. Epub 2013 Jul 26.
8
A randomized double blind placebo controlled clinical trial of N-Acetylcysteine added to risperidone for treating autistic disorders.一项关于 N-乙酰半胱氨酸联合利培酮治疗自闭症障碍的随机双盲安慰剂对照临床试验。
BMC Psychiatry. 2013 Jul 25;13:196. doi: 10.1186/1471-244X-13-196.
9
Immunological and autoimmune considerations of Autism Spectrum Disorders.自闭症谱系障碍的免疫学和自身免疫考虑。
J Autoimmun. 2013 Aug;44:1-7. doi: 10.1016/j.jaut.2013.05.005. Epub 2013 Jul 15.
10
Enrichment of elevated plasma F2t-isoprostane levels in individuals with autism who are stratified by presence of gastrointestinal dysfunction.自闭症患者存在胃肠功能障碍时,其血浆 F2t-异前列烷水平升高。
PLoS One. 2013 Jul 3;8(7):e68444. doi: 10.1371/journal.pone.0068444. Print 2013.

将自闭症患者大脑中的氧化应激、线粒体功能障碍和炎症联系起来的证据。

Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism.

作者信息

Rossignol Daniel A, Frye Richard E

机构信息

Rossignol Medical Center Irvine, CA, USA.

Department of Pediatrics, Arkansas Children's Hospital Research Institute, University of Arkansas for Medical Sciences Little Rock, AR, USA.

出版信息

Front Physiol. 2014 Apr 22;5:150. doi: 10.3389/fphys.2014.00150. eCollection 2014.

DOI:10.3389/fphys.2014.00150
PMID:24795645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4001006/
Abstract

Autism spectrum disorders (ASDs) are a heterogeneous group of neurodevelopmental disorders that are defined solely on the basis of behavioral observations. Therefore, ASD has traditionally been framed as a behavioral disorder. However, evidence is accumulating that ASD is characterized by certain physiological abnormalities, including oxidative stress, mitochondrial dysfunction and immune dysregulation/inflammation. While these abnormalities have been reported in studies that have examined peripheral biomarkers such as blood and urine, more recent studies have also reported these abnormalities in brain tissue derived from individuals diagnosed with ASD as compared to brain tissue derived from control individuals. A majority of these brain tissue studies have been published since 2010. The brain regions found to contain these physiological abnormalities in individuals with ASD are involved in speech and auditory processing, social behavior, memory, and sensory and motor coordination. This manuscript examines the evidence linking oxidative stress, mitochondrial dysfunction and immune dysregulation/inflammation in the brain of ASD individuals, suggesting that ASD has a clear biological basis with features of known medical disorders. This understanding may lead to new testing and treatment strategies in individuals with ASD.

摘要

自闭症谱系障碍(ASD)是一组异质性神经发育障碍,仅根据行为观察来定义。因此,传统上ASD被视为一种行为障碍。然而,越来越多的证据表明,ASD具有某些生理异常特征,包括氧化应激、线粒体功能障碍和免疫失调/炎症。虽然这些异常在研究外周生物标志物(如血液和尿液)的研究中已有报道,但最近的研究也报告称,与来自对照个体的脑组织相比,被诊断为ASD的个体的脑组织中也存在这些异常。这些脑组织研究中的大多数是自2010年以来发表的。在患有ASD的个体中发现含有这些生理异常的脑区涉及言语和听觉处理、社会行为、记忆以及感觉和运动协调。本手稿研究了将ASD个体大脑中的氧化应激、线粒体功能障碍和免疫失调/炎症联系起来的证据,表明ASD具有明确的生物学基础,具有已知医学疾病的特征。这种认识可能会为ASD个体带来新的检测和治疗策略。