Oxidative stress marker aberrations in children with autism spectrum disorder: a systematic review and meta-analysis of 87 studies (N=9109)

被引:90
|
作者
Chen, Lei [1 ]
Shi, Xiao-Jie [1 ]
Liu, Hua [1 ]
Mao, Xiao [2 ]
Gui, Lue-Ning [1 ]
Wang, Hua [2 ]
Cheng, Yong [1 ,2 ]
机构
[1] Minzu Univ China, Coll Life & Environm Sci, Ctr Translat Neurosci, Key Lab Ethnomed,Minist Educ, Beijing, Peoples R China
[2] Hunan Prov Maternal & Child Hlth Care Hosp, NHC Key Lab Birth Defects Res Prevent & Treatment, Changsha, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTIOXIDANT CAPACITY; NEUROTROPHIC FACTOR; PERIPHERAL-BLOOD; CYTOKINE LEVELS; SUPPLEMENTATION; METABOLISM; BIOMARKERS; DISEASE; ASSOCIATION; DIAGNOSIS;
D O I
10.1038/s41398-020-01135-3
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
There is increasing awareness that oxidative stress may be implicated in the pathophysiology of autism spectrum disorder (ASD). Here we aimed to investigate blood oxidative stress marker profile in ASD children by a meta-analysis. Two independent investigators systematically searched Web of Science, PubMed, and Cochrane Library and extracted data from 87 studies with 4928 ASD children and 4181 healthy control (HC) children. The meta-analysis showed that blood concentrations of oxidative glutathione (GSSG), malondialdehyde, homocysteine, S-adenosylhomocysteine, nitric oxide, and copper were higher in children with ASD than that of HC children. In contrast, blood reduced glutathione (GSH), total glutathione (tGSH), GSH/GSSG, tGSH/GSSG, methionine, cysteine, vitamin B9, vitamin D, vitamin B12, vitamin E, S-adenosylmethionine/S-adenosylhomocysteine, and calcium concentrations were significantly reduced in children with ASD relative to HC children. However, there were no significance differences between ASD children and HC children for the other 17 potential markers. Heterogeneities among studies were found for most markers, and meta-regressions indicated that age and publication year may influence the meta-analysis results. These results therefore clarified blood oxidative stress profile in children with ASD, strengthening clinical evidence of increased oxidative stress implicating in pathogenesis of ASD. Additionally, given the consistent and large effective size, glutathione metabolism biomarkers have the potential to inform early diagnosis of ASD.
引用
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页数:10
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