MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Veena S. Patel - , Lovelace Biomedical Research Institute (Autor:in)
  • Sinead Kelly - , Trinity College Dublin (Autor:in)
  • Carrie Wright - , Lovelace Biomedical Research Institute, University of New Mexico (Autor:in)
  • Cota Navin Gupta - , Lovelace Biomedical Research Institute (Autor:in)
  • Alejandro Arias-Vasquez - , Klinik und Poliklinik für Kinder- und Jugendmedizin (Autor:in)
  • Nora Perrone-Bizzozero - , University of New Mexico (Autor:in)
  • Stefan Ehrlich - , Klinik und Poliklinik für Kinder- und Jugendpsychiatrie (Autor:in)
  • Lei Wang - , Northwestern University (Autor:in)
  • Juan R. Bustillo - , University of New Mexico (Autor:in)
  • Derek Morris - , Trinity College Dublin, University of Galway (Autor:in)
  • Aiden Corvin - , Trinity College Dublin (Autor:in)
  • Dara M. Cannon - , University of Galway (Autor:in)
  • Colm McDonald - , University of Galway (Autor:in)
  • Gary Donohoe - , Trinity College Dublin, University of Galway (Autor:in)
  • Vince D. Calhoun - , Lovelace Biomedical Research Institute, University of New Mexico (Autor:in)
  • Jessica A. Turner - , Lovelace Biomedical Research Institute, Georgia State University (Autor:in)

Abstract

Genome-wide association studies implicate the MIR137HG risk variant rs1625579 (MIR137HGrv) within the host gene for microRNA-137 as a potential regulator of schizophrenia susceptibility. We examined the influence of MIR137HGrv genotype on 17 subcortical and callosal volumes in a large sample of individuals with schizophrenia and healthy controls (n = 841). Although the volumes were overall reduced relative to healthy controls, for individuals with schizophrenia the homozygous MIR137HGrv risk genotype was associated with attenuated reduction of mid-posterior corpus callosum volume (p = 0.001), along with trend-level effects in the adjacent central and posterior corpus callosum. These findings are unique in the literature and remain robust after analysis in ethnically homogenous and single-scanner subsets of the larger sample. Thus, our study suggests that the mechanisms whereby MIR137HGrv works to increase schizophrenia risk are not those that generate the corpus callosum volume reductions commonly found in the disorder.

Details

OriginalspracheEnglisch
Seiten (von - bis)44-49
Seitenumfang6
FachzeitschriftNeuroscience letters
Jahrgang602
PublikationsstatusVeröffentlicht - 8 Aug. 2015
Peer-Review-StatusJa

Externe IDs

PubMed 26123324
ORCID /0000-0003-2132-4445/work/160950843

Schlagworte

ASJC Scopus Sachgebiete

Schlagwörter

  • Corpus callosum, MicroRNA-137, MIR137, Multi-site, Schizophrenia, Subcortical volume