Exome-wide association study identified genetic variants contributing to the risk of cerebral palsy

Author:

Xing Qinghe1,Cheng Ye1ORCID,Xu Yiran2,Li Hongwei2,Qiao Yimeng2,Wang Yangong1,Su Yu1,Zhang Jin1,Wang Xiaoyang3,Zhu Changlian4ORCID

Affiliation:

1. Children's hospital of Fudan University; and Institutes of Biomedical Sciences of Fudan University

2. Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, The Third Affiliated Hospital and Institute of Neuroscience of Zhengzhou University

3. University of Gothenburg

4. Gö

Abstract

Abstract Cerebral palsy (CP) is the most common physical disability in childhood that results from the interaction of environmental and genetic factors. Yet in many patients, the etiology remains unknown. We identified significant association at rs3131787 within the human leukocyte antigen (HLA) region using two-stage association study between 1,090 CP cases and 1,100 controls. Fine mapping of the HLA region indicated that the carrier frequency of HLA-B*13:02 was significantly higher in CP, particularly in CP without preterm birth, low birth weight, birth asphyxia or periventricular leukomalacia (PVL). DRB1*07:01/DQA1*02:01 was also significantly enriched in CP and more specifically in dyskinetic type. Additionally, significant enrichment of carrier frequency was detected for HLA-A*32:01 in CP with either preterm birth or low birth weight and for HLA-B*27:05 in CP with birth asphyxia. These data suggest that immune dysregulation resulting from immunogenetic variants or environmental exposures may underlie the pathogenesis of CP.

Publisher

Research Square Platform LLC

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