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Transl Psychiatry ; 7(5): e1140, 2017 05 30.
Article in English | MEDLINE | ID: mdl-28556829

ABSTRACT

Major depressive disorder (MDD) has been linked to differences in the volume of certain areas of the brain and to variants in the piccolo presynaptic cytomatrix protein (PCLO), but the relationship between PCLO and brain morphology has not been studied. A single-nucleotide polymorphism (SNP) in PCLO, rs2522833, is thought to affect protein stability and the activity of the hypothalamic-pituitary-adrenal axis. We investigated the relationship between cortical volume and this SNP in first-episode, drug-naive patients with MDD or healthy control subjects. Seventy-eight participants, including 30 patients with MDD and 48 healthy control subjects, were recruited via interview. PCLO rs2522833 genotyping and plasma cortisol assays were performed, and gray matter volume was estimated using structural magnetic resonance images. Among the individuals carrying the C-allele of PCLO rs2522833, the volume of the left temporal pole was significantly smaller in those with MDD than in healthy controls (family-wise error-corrected, P=0.003). No differences were detected in other brain regions. In addition, the C-carriers showed a larger volume reduction in the left temporal pole than those in the individuals with A/A genotype (P=0.0099). Plasma cortisol levels were significantly higher in MDD-affected C-carriers than in the healthy control C-carriers (12.76±6.10 vs 9.31±3.60 nm, P=0.045). We conclude that PCLO SNP rs2522833 is associated with a gray matter volume reduction in the left temporal pole in drug-naive, first-episode patients with MDD carrying the C-allele.


Subject(s)
Brain/diagnostic imaging , Cytoskeletal Proteins/genetics , Depressive Disorder, Major/metabolism , Gray Matter/diagnostic imaging , Neuropeptides/genetics , Adult , Alleles , Brain/pathology , Depressive Disorder, Major/physiopathology , Female , Genetic Predisposition to Disease , Genome-Wide Association Study , Genotype , Gray Matter/pathology , Humans , Hydrocortisone/blood , Hypothalamo-Hypophyseal System/metabolism , Hypothalamo-Hypophyseal System/physiopathology , Japan/epidemiology , Magnetic Resonance Imaging/methods , Male , Mental Status and Dementia Tests , Middle Aged , Pituitary-Adrenal System/metabolism , Pituitary-Adrenal System/physiopathology , Polymorphism, Single Nucleotide/genetics , Prospective Studies
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