Literature DB >> 24373612

ITIH3 polymorphism may confer susceptibility to psychiatric disorders by altering the expression levels of GLT8D1.

Daimei Sasayama1, Hiroaki Hori2, Noriko Yamamoto2, Seiji Nakamura3, Toshiya Teraishi2, Masahiko Tatsumi4, Kotaro Hattori2, Miho Ota2, Teruhiko Higuchi5, Hiroshi Kunugi6.   

Abstract

A recent genome-wide analysis indicated that a polymorphism (rs2535629) of ITIH3 showed the strongest association signal with susceptibility to psychiatric disorders in Caucasian populations. The aim of the study was to replicate the association of rs2535629 with schizophrenia and major depressive disorder (MDD) in Japanese subjects. A total of 611 patients with schizophrenia, 868 with MDD, and 1193 healthy controls were successfully genotyped for rs2535629. A significant difference in allele distribution was found between patients with schizophrenia and controls (odds ratio [OR] = 1.21, 95% confidence interval [CI]: 1.05-1.39, P = 0.0077). A similar trend was found for patients with MDD (OR = 1.11, 95% CI: 0.98-1.26, P = 0.092). The allele distribution in the combined patient group (schizophrenia and MDD) was significantly different from that of the control group (OR = 1.15, 95% CI: 1.03-1.28, P = 0.011). Gene expression microarray analysis of whole blood samples in 39 MDD patients and 40 healthy controls showed that rs2535629 has a strong influence on the expression levels of ITIH4 and GLT8D1. The expression levels of GLT8D1 were significantly higher in patients with MDD than in controls (P = 0.021). To our knowledge, the present study showed for the first time the association of rs2535629 with psychiatric disorders in an Asian population. Our findings suggest that rs2535629 influences the susceptibility to psychiatric disorders by affecting the expression level of GLT8D1.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  GLT8D1; Gene expression; ITIH3; ITIH4; Major depressive disorder; Microarray; Schizophrenia; Single nucleotide polymorphism

Mesh:

Substances:

Year:  2013        PMID: 24373612     DOI: 10.1016/j.jpsychires.2013.12.002

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  14 in total

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Journal:  Cell Rep       Date:  2019-02-26       Impact factor: 9.423

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Journal:  Sci Rep       Date:  2020-03-23       Impact factor: 4.379

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Journal:  Nat Commun       Date:  2018-02-26       Impact factor: 14.919

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