Association and epistatic analysis of white matter related genes across the continuum schizophrenia and autism spectrum disorders: The joint effect of NRG1-ErbB genes.
White matter
autism spectrum disorders
gene–gene interaction
myelin
oligodendrocyte
schizophrenia
Journal
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry
ISSN: 1814-1412
Titre abrégé: World J Biol Psychiatry
Pays: England
ID NLM: 101120023
Informations de publication
Date de publication:
03 2022
03 2022
Historique:
pubmed:
3
8
2021
medline:
27
10
2022
entrez:
2
8
2021
Statut:
ppublish
Résumé
Schizophrenia-spectrum disorders (SSD) and Autism spectrum disorders (ASD) are neurodevelopmental disorders that share clinical, cognitive, and genetic characteristics, as well as particular white matter (WM) abnormalities. In this study, we aimed to investigate the role of a set of oligodendrocyte/myelin-related (OMR) genes and their epistatic effect on the risk for SSD and ASD. We examined 108 SNPs in a set of 22 OMR genes in 1749 subjects divided into three independent samples (187 SSD trios, 915 SSD cases/control, and 91 ASD trios). Genetic association and gene-gene interaction analyses were conducted with PLINK and MB-MDR, and permutation procedures were implemented in both. Some OMR genes showed an association trend with SSD, while after correction, the ones that remained significantly associated were Our results suggest the implication of OMR genes in the risk for both SSD and ASD and highlight the role of
Sections du résumé
BACKGROUND
Schizophrenia-spectrum disorders (SSD) and Autism spectrum disorders (ASD) are neurodevelopmental disorders that share clinical, cognitive, and genetic characteristics, as well as particular white matter (WM) abnormalities. In this study, we aimed to investigate the role of a set of oligodendrocyte/myelin-related (OMR) genes and their epistatic effect on the risk for SSD and ASD.
METHODS
We examined 108 SNPs in a set of 22 OMR genes in 1749 subjects divided into three independent samples (187 SSD trios, 915 SSD cases/control, and 91 ASD trios). Genetic association and gene-gene interaction analyses were conducted with PLINK and MB-MDR, and permutation procedures were implemented in both.
RESULTS
Some OMR genes showed an association trend with SSD, while after correction, the ones that remained significantly associated were
DISCUSSION
Our results suggest the implication of OMR genes in the risk for both SSD and ASD and highlight the role of
Identifiants
pubmed: 34338147
doi: 10.1080/15622975.2021.1939155
doi:
Substances chimiques
NRG1 protein, human
0
Neuregulin-1
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM