A Systematic Investigation of Complement and Coagulation-Related Protein in Autism Spectrum Disorder Using Multiple Reaction Monitoring Technology.
10.1007/s12264-023-01055-4
- Author:
Xueshan CAO
1
;
Xiaoxiao TANG
1
;
Chengyun FENG
2
;
Jing LIN
1
;
Huajie ZHANG
1
;
Qiong LIU
1
;
Qihong ZHENG
1
;
Hongbin ZHUANG
1
;
Xukun LIU
1
;
Haiying LI
3
;
Naseer Ullah KHAN
1
;
Liming SHEN
4
Author Information
1. College of Life Science and Oceanography, Shenzhen University, Shenzhen, 518060, China.
2. Maternal and Child Health Hospital of Baoan, Shenzhen, 518100, China.
3. Department of Endocrinology, Guiyang First People's Hospital, Guiyang, 550002, China.
4. College of Life Science and Oceanography, Shenzhen University, Shenzhen, 518060, China. slm@szu.edu.cn.
- Publication Type:Journal Article
- Keywords:
Autism spectrum disorder;
Biomarker;
Complement and coagulation cascade;
Complement system;
Machine learning;
Multiple reaction monitoring
- MeSH:
Child;
Humans;
Autism Spectrum Disorder/metabolism*;
Proteomics;
Brain/metabolism*
- From:
Neuroscience Bulletin
2023;39(11):1623-1637
- CountryChina
- Language:English
-
Abstract:
Autism spectrum disorder (ASD) is one of the common neurodevelopmental disorders in children. Its etiology and pathogenesis are poorly understood. Previous studies have suggested potential changes in the complement and coagulation pathways in individuals with ASD. In this study, using multiple reactions monitoring proteomic technology, 16 of the 33 proteins involved in this pathway were identified as differentially-expressed proteins in plasma between children with ASD and controls. Among them, CFHR3, C4BPB, C4BPA, CFH, C9, SERPIND1, C8A, F9, and F11 were found to be altered in the plasma of children with ASD for the first time. SERPIND1 expression was positively correlated with the CARS score. Using the machine learning method, we obtained a panel composed of 12 differentially-expressed proteins with diagnostic potential for ASD. We also reviewed the proteins changed in this pathway in the brain and blood of patients with ASD. The complement and coagulation pathways may be activated in the peripheral blood of children with ASD and play a key role in the pathogenesis of ASD.
