| Literature DB >> 35348996 |
Yuxi Zhao1, Xueshan Cao2, Liming Shen3, Huajie Zhang3,4, Jing Lin3,5, Yan Gao6, Margy Chen7, Naseer Ullah Khan3, Xiaoxiao Tang3, Qi Hong6, Chengyun Feng6.
Abstract
Autism spectrum disorder (ASD) has become one of the most common neurological developmental disorders in children. However, the study of ASD diagnostic markers faces significant challenges due to the existence of heterogeneity. In this study, genetic testing was performed on children who were clinically diagnosed with ASD. Children with ASD susceptibility genes and healthy controls were studied. The proteomics of plasma and peripheral blood mononuclear cells (PBMCs) as well as plasma metabolomics were carried out. The results showed that although there was genetic heterogeneity in children with ASD, the differentially expressed proteins (DEPs) in plasma, peripheral blood mononuclear cells, and differential metabolites in plasma could still effectively distinguish autistic children from controls. The mechanism associated with them focuses on several common and previously reported mechanisms of ASD. The biomarkers for ASD diagnosis could be found by taking differentially expressed proteins and differential metabolites into consideration. Integrating omics data, glycerophospholipid metabolism and N-glycan biosynthesis might play a critical role in the pathogenesis of ASD.Entities:
Keywords: Autism spectrum disorder; Biomarker; Heterogeneity; Metabolomics; Peripheral blood mononuclear cells; Plasma; Proteomics
Mesh:
Year: 2022 PMID: 35348996 DOI: 10.1007/s12035-022-02801-x
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590