| Literature DB >> 26014434 |
Ivan Chavarria-Siles1,2,3, Tonya White4,5, Christiaan de Leeuw1,2, Andrea Goudriaan6, Esther Lips1, Stefan Ehrlich7,8, Jessica A Turner9,10, Vince D Calhoun10,11,12, Randy L Gollub7,13, Vincent A Magnotta14, Beng-Choon Ho15, August B Smit6, Mark H G Verheijen6, Danielle Posthuma1,2,4.
Abstract
Disruptions in white matter (WM) tract structures have been implicated consistently in the pathophysiology of schizophrenia. Global WM integrity--as measured by fractional anisotropy (FA)--is highly heritable and may provide a good endophenotype for genetic studies of schizophrenia. WM abnormalities in schizophrenia are not localized to one specific brain region but instead reflect global low-level decreases in FA coupled with focal abnormalities. In this study, we sought to investigate whether functional gene sets associated with schizophrenia are also associated with WM integrity. We analyzed FA and genetic data from the Mind Research Network Clinical Imaging Consortium to study the effect of multiple oligodendrocyte gene sets on schizophrenia and WM integrity using a functional gene set analysis in 77 subjects with schizophrenia and 104 healthy controls. We found that a gene set involved in myelination was significantly associated with schizophrenia and FA. This gene set includes 17 genes that are expressed in oligodendrocytes and one neuronal gene (NRG1) that is known to regulate myelination. None of the genes within the gene set were associated with schizophrenia or FA individually, suggesting that no single gene was driving the association of the gene set. Our findings support the hypothesis that multiple genetic variants in myelination-related genes contribute to the observed correlation between schizophrenia and decreased WM integrity as measured by FA.Entities:
Mesh：
Year: 2015 PMID： 26014434 PMCID： PMC4757770 DOI： 10.1038/ejhg.2015.120
Source DB: PubMed Journal: Eur J Hum Genet ISSN： 1018-4813 Impact factor: 4.246