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Myelin-Associated Glycoprotein Gene and Brain Morphometry in Schizophrenia

Bibliographic Data

ID15519057
AuthorsDaniel Felsky (0000-0003-1831-9848, Centre for Addiction and Mental Health, corresponding author), Aristotle N Voineskos (0000-0003-0156-0395, Centre for Addiction and Mental Health), Jason P Lerch (0000-0001-6164-2881, Hospital for Sick Children), Arash Nazeri (0000-0001-6983-0641, Tehran University of Medical Sciences), Sajid A Shaikh (0000-0001-5556-2957, Centre for Addiction and Mental Health), Tarek K Rajji (0000-0002-8324-2560, Centre for Addiction and Mental Health), Benoit H Mulsant (0000-0002-0303-6450, Centre for Addiction and Mental Health), James L Kennedy (0000-0002-8733-3806, Centre for Addiction and Mental Health)
Year2012
Volume3
Pages40-40
Publication date2012-01-01
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2012.00040
PMID22563322
PMCIDPMC3342517
OpenAlexW2140387265
LanguageEN
Citations received1
References cited4

Myelin and oligodendrocyte disruption may be a core feature of schizophrenia pathophysiology. The purpose of the present study was to localize the effects of previously identified risk variants in the myelin-associated glycoprotein (MAG) gene on brain morphometry in schizophrenia patients and healthy controls. Forty-five schizophrenia patients and 47 matched healthy controls underwent clinical, structural magnetic resonance imaging, and genetics procedures. Gray and white matter cortical lobe volumes along with hippocampal volumes were calculated from T1-weighted MRI scans. Each subject was also genotyped for the two disease-associated MAG single nucleotide polymorphisms (rs720308 and rs720309). Repeated measures general linear model (GLM) analysis found significant region by genotype and region by genotype by diagnosis interactions for the effects of MAG risk variants on lobar gray matter volumes. No significant associations were found with lobar white matter volumes or hippocampal volumes. Follow-up univariate GLMs found the AA genotype of rs720308 predisposed schizophrenia patients to left temporal and parietal gray matter volume deficits. These results suggest that the effects of the MAG gene on cortical gray matter volume in schizophrenia patients can be localized to temporal and parietal cortices. Our results support a role for MAG gene variation in brain morphometry in schizophrenia, align with other lines of evidence implicating MAG in schizophrenia, and provide genetically based insight into the heterogeneity of brain imaging findings in this disorder

Biology · Brain morphometry · Central nervous system · Gene · Glycoprotein · Magnetic resonance imaging · Myelin · Myelin-associated glycoprotein · Psychiatry · Schizophrenia (object-oriented programming · Advanced Neuroimaging Techniques and Applications · Axon Guidance and Neuronal Signaling · Glycosylation and Glycoproteins Research · Medicine · Neuroscience · Psychology · Genetics

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Citations per year0.14
Citation span2019 - 2019 (1)
Highly citedNo

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