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PRODH Polymorphisms, Cortical Volumes and Thickness in Schizophrenia
Author(s) -
Vanessa Kiyomi Ota,
Fernanda T. Bellucco,
Ary Gadelha,
Marcos Santoro,
Cristiano Noto,
Denise Maria Christofolini,
Idaiane Assunção,
Karen M. Yamada,
Ândrea RibeirodosSantos,
Sidney Emanuel Batista dos Santos,
Jair de Jesus Mari,
Marı́lia de Arruda Cardoso Smith,
Maria Isabel Melaragno,
Rodrigo A. Bressan,
João Ricardo Sato,
Andrea Parolin Jackowski,
Síntia Belangero
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0087686
Subject(s) - positive and negative syndrome scale , schizophrenia (object oriented programming) , sanger sequencing , genetics , restriction fragment length polymorphism , allele , genotype , heritability , neurochemical , functional magnetic resonance imaging , medicine , biology , psychosis , gene , neuroscience , psychiatry , mutation
Schizophrenia is a neurodevelopmental disorder with high heritability. Several lines of evidence indicate that the PRODH gene may be related to the disorder. Therefore, our study investigates the effects of 12 polymorphisms of PRODH on schizophrenia and its phenotypes. To further evaluate the roles of the associated variants in the disorder, we have conducted magnetic resonance imaging (MRI) scans to assess cortical volumes and thicknesses. A total of 192 patients were evaluated using the Structured Clinical Interview for DSM-IV (SCID), Positive and Negative Syndrome Scale (PANSS), Calgary Depression Scale, Global Assessment of Functioning (GAF) and Clinical Global Impression (CGI) instruments. The study included 179 controls paired by age and gender. The samples were genotyped using the real-time polymerase chain reaction (PCR), restriction fragment length polymorphism (RFLP)-PCR and Sanger sequencing methods. A sample of 138 patients and 34 healthy controls underwent MRI scans. One polymorphism was associated with schizophrenia (rs2904552), with the G-allele more frequent in patients than in controls. This polymorphism is likely functional, as predicted by PolyPhen and SIFT, but it was not associated with brain morphology in our study. In summary, we report a functional PRODH variant associated with schizophrenia that may have a neurochemical impact, altering brain function, but is not responsible for the cortical reductions found in the disorder.

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