4.7 Article

DTNBP1 Is Associated with Imaging Phenotypes in Schizophrenia

Journal

HUMAN BRAIN MAPPING
Volume 30, Issue 11, Pages 3783-3794

Publisher

WILEY
DOI: 10.1002/hbm.20806

Keywords

magnetic resonance imaging (MRI); dysbindin; genetic marker; polymorphism; cortical thickness; brain structure; morphology; gray matter

Funding

  1. NCRR NIH HHS [P41 RR13642, U54 RR021813-05, P41 RR013642, U54 RR021813, P41 RR013642-12, UL1 RR024911, UL1 RR024911-01] Funding Source: Medline
  2. NIMH NIH HHS [K23 MH001760, R01 MH060004, R01 MH079800, K01 MH065580, K99 MH086756, K01 MH073990, R01 MH060374-05, R01 MH060004-09, K01 MH073990-04, R00 MH086756-03, K99 MH086756-01, K23 MH001760-05, R00 MH086756, R01 MH079800-05, K99 MH086756-02, K01 MH065580-05, R01 MH060374, MH001760, MH079800] Funding Source: Medline

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Dystrobrevin binding protein 1 (DTNBP1) has been identified as putative schizophrenia susceptibility gene, but it remains unknown whether polymorphisms relate to altered cerebral structure. We examined relationships between a previously implicated DTNBP1 risk variant [P15781 and global and segmented brain tissue volumes and regional cortical thickness in schizophrenia (n = 62; 24 risk carriers) and healthy subjects (n = 42; 11 risk carriers), across ethnic groups and within Caucasians. Schizophrenia patients showed similar brain volumes, but significantly reduced brain-size adjusted gray matter and CSF volumes and cortical thinning in a widespread neocortical distribution compared to controls. DTNBP1 risk was found associated with reduced brain volume, but not with tissue sub-compartments. Cortical thickness, which was weakly associated with brain size, showed regional variations in association with genetic risk, although effects were dominated by highly significant genotype by diagnosis interactions over broad areas of cortex. Risk status was found associated with regional cortical thinning in patients, particularly in temporal networks, but with thickness increases in controls. DTNBP1 effects for brain volume and cortical thickness appear driven by different neurobiological processes. Smaller brain volumes observed in risk carriers may relate to previously reported DTNBP1/cognitive function relationships irrespective of diagnosis. Regional cortical thinning in patient, but not in control risk carriers, may suggest that DTNBP1 interacts with other schizophrenia-related risk factors to affect laminar thickness. Alternatively, DTNBP1 may influence neural processes for which individuals with thicker cortex are less vulnerable. Although DTNBP1 relates to cortical thinning in schizophrenia, morphological changes in the disorder are influenced by additional genetic and/or environmental factors. Hum Brain Mapp 30:3783-3794, 2009. (C) 2009 Wiley-Liss, Inc.

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