Myelination-related genes are associated with decreased white matter integrity in schizophrenia

Ivan Chavarria-Siles, Tonya White, Christiaan De Leeuw, Andrea Goudriaan, Esther Lips, Stefan Ehrlich, Jessica A. Turner, Vince D. Calhoun, Randy L. Gollub, Vincent A. Magnotta, Eng Choon Ho, August B. Smit, Mark H.G. Verheijen, Danielle Posthuma

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


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.

Original languageEnglish (US)
Pages (from-to)381-386
Number of pages6
JournalEuropean Journal of Human Genetics
Issue number3
StatePublished - Mar 1 2016

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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