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Published in: Behavioral and Brain Functions 1/2011

Open Access 01-12-2011 | Research

The genetic validation of heterogeneity in schizophrenia

Authors: Atsushi Tsutsumi, Stephen J Glatt, Tetsufumi Kanazawa, Seiya Kawashige, Hiroyuki Uenishi, Akira Hokyo, Takao Kaneko, Makiko Moritani, Hiroki Kikuyama, Jun Koh, Hitoshi Matsumura, Hiroshi Yoneda

Published in: Behavioral and Brain Functions | Issue 1/2011

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Abstract

Introduction

Schizophrenia is a heritable disorder, however clear genetic architecture has not been detected. To overcome this state of uncertainty, the SZGene database has been established by including all published case-control genetic association studies appearing in peer-reviewed journals. In the current study, we aimed to determine if genetic variants strongly suggested by SZGene are associated with risk of schizophrenia in our case-control samples of Japanese ancestry. In addition, by employing the additive model for aggregating the effect of seven variants, we aimed to verify the genetic heterogeneity of schizophrenia diagnosed by an operative diagnostic manual, the DSM-IV.

Methods

Each positively suggested genetic polymorphism was ranked according to its p-value, then the seven top-ranked variants (p < 0.0005) were selected from DRD2, DRD4, GRIN2B, TPH1, MTHFR, and DTNBP1 (February, 2007). 407 Schizophrenia cases and 384 controls participated in this study. To aggregate the vulnerability of the disorder based on the participants' genetic information, we calculated the "risk-index" by adding the number of genetic risk factors.

Results

No statistically significant deviation between cases and controls was observed in the genetic risk-index derived from all seven variants on the top-ranked polymorphisms. In fact, the average risk-index score in the schizophrenia group (6.5+/-1.57) was slightly lower than among controls (6.6+/-1.39).

Conclusion

The current work illustrates the difficulty in identifying universal and definitive risk-conferring polymorphisms for schizophrenia. Our employed number of samples was small, so we can not preclude the possibility that some or all of these variants are minor risk factors for schizophrenia in the Japanese population. It is also important to aggregate the updated positive variants in the SZGene database when the replication work is conducted.
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Metadata
Title
The genetic validation of heterogeneity in schizophrenia
Authors
Atsushi Tsutsumi
Stephen J Glatt
Tetsufumi Kanazawa
Seiya Kawashige
Hiroyuki Uenishi
Akira Hokyo
Takao Kaneko
Makiko Moritani
Hiroki Kikuyama
Jun Koh
Hitoshi Matsumura
Hiroshi Yoneda
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Behavioral and Brain Functions / Issue 1/2011
Electronic ISSN: 1744-9081
DOI
https://doi.org/10.1186/1744-9081-7-43

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