Author/Authors :
Masayuki Ide، نويسنده , , Tatsuyuki Muratake، نويسنده , , Kazuo Yamada، نويسنده , , Yoshimi Iwayama-Shigeno، نويسنده , , Kazuya Iwamoto، نويسنده , , Hitomi Takao، نويسنده , , Tomoko Toyota، نويسنده , , Naoshi Kaneko، نويسنده , , Yoshio Minabe، نويسنده , , Kazuhiko Nakamura، نويسنده , , Tadafumi Kato، نويسنده , , Norio Mori، نويسنده , , Takashi Asada، نويسنده , , Toshiyuki Someya، نويسنده , , Takeo Yoshikawa، نويسنده ,
Abstract :
Background
Wnt signaling plays important roles in neurodevelopmental processes. Frizzled is a receptor of Wnt protein, and the Frizzled 3 (FZD3) gene was recently reported to be associated with schizophrenia. Our study attempted to confirm associations between FZD3 and schizophrenia in Japanese family and case–control samples.
Methods
Genetic associations were evaluated using family-based transmission tests (212 families, 643 subjects) and case–control analysis (540 schizophrenia patients, 540 control sample). Six single nucleotide polymorphisms (SNPs) on the FZD3 locus were genotyped, and levels of FZD3 mRNA expression in postmortem brains were examined.
Results
Neither family- nor population-based studies supported associations between FZD3 and schizophrenia. FZD3 expression was unaltered in schizophrenic brains.
Conclusions
Although two prior studies have reported associations using limited numbers of SNPs on FZD3, our intensive study failed to support any major contribution of FZD3 to schizophrenia susceptibility.
Keywords :
family-based association study , neurodevelopment , postmortem brain , real-time quantitative RTPCR , WNT SIGNALING , Case–control study