Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia

Panos Roussos, Pavel Katsel, Kenneth L. Davis, Panos Bitsios, Jigar Jogia, Stella G. Giakoumaki, Kinga Rozsnyai, David Collier, Sophia Frangou, Larry J. Siever, Vahram Haroutunian

Research output: Contribution to journalArticle

Abstract

Context: Genetic, neuroimaging, and molecular neurobiological evidence support the hypothesis that the disconnectivity syndrome in schizophrenia (SZ) could arise from failures of saltatory conduction and abnormalities at the nodes of Ranvier (NOR) interface where myelin and axons interact. Objective: To identify abnormalities in the expression of oligodendroglial genes and proteins that participate in the formation, maintenance, and integrity of the NOR in SZ. Design: The messenger RNA (mRNA) expression levels of multiple NOR genes were quantified in 2 independent postmortem brain cohorts of individuals with SZ, and generalizability to protein expression was confirmed. The effect of the ANK3 genotype on the mRNA expression level was tested in postmortem human brain. Case-control analysis tested the association of the ANK3 genotype with SZ. The ANK3 genotype's influence on cognitive task performance and functional magnetic resonance imaging activation was tested in 2 independent cohorts of healthy individuals. Setting: Research hospital. Patients: Postmortem samples from patients with SZ and healthy controls were used for the brain expression study (n=46) and the case-control analysis (n=272). Healthy white men and women participated in the cognitive (n=513) and neuroimaging (n=52) studies. Main Outcome Measures: The mRNA and protein levels in postmortem brain samples, genetic association with schizophrenia, cognitive performance, and blood oxygenation level-dependent functional magnetic resonance imaging. Results: The mRNA expression of multiple NOR genes was decreased in schizophrenia. The ANK3 rs9804190 C allele was associated with lower ANK3 mRNA expression levels, higher risk for SZ in the case-control cohort, and poorer working memory and executive function performance and increased prefrontal activation during a working memory task in healthy individuals. Conclusions: These results point to abnormalities in the expression of genes and protein associated with the integrity of the NOR and suggest them as substrates for the disconnectivity syndrome in SZ. The association of ANK3 with lower brain mRNA expression levels implicates a molecular mechanism for its genetic, clinical, and cognitive associations with SZ.
Original languageEnglish
Pages (from-to)7-15
Number of pages9
JournalArchives of General Psychiatry
Volume69
Issue number1
Early online date5 Sep 2011
DOIs
Publication statusPublished - Jan 2012

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    Roussos, P., Katsel, P., Davis, K. L., Bitsios, P., Jogia, J., Giakoumaki, S. G., Rozsnyai, K., Collier, D., Frangou, S., Siever, L. J., & Haroutunian, V. (2012). Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia. Archives of General Psychiatry, 69(1), 7-15. https://doi.org/10.1001/archgenpsychiatry.2011.110