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No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

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  • Emma C Johnson
  • Douglas W Bjelland
  • Daniel P Howrigan
  • Abdel Abdellaoui
  • Gerome Breen
  • Anders Borglum
  • Sven Cichon
  • Franziska Degenhardt
  • Andreas J Forstner
  • Josef Frank
  • Giulio Genovese
  • Stefanie Heilmann-Heimbach
  • Stefan Herms
  • Per Hoffman
  • Wolfgang Maier
  • Manuel Mattheisen
  • Derek Morris
  • Bryan Mowry
  • Betram Müller-Mhysok
  • Benjamin Neale
  • Igor Nenadic
  • Markus M Nöthen
  • Colm O'Dushlaine
  • Marcella Rietschel
  • Douglas M Ruderfer
  • Dan Rujescu
  • Thomas G Schulze
  • Matthew A Simonson
  • Eli Stahl
  • Jana Strohmaier
  • Stephanie H Witt
  • Patrick F Sullivan
  • Matthew C Keller
  • Schizophrenia Working Group of the Psychiatric Genomics Consortium
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It is well known that inbreeding increases the risk of recessive monogenic diseases, but it is less certain whether it contributes to the etiology of complex diseases such as schizophrenia. One way to estimate the effects of inbreeding is to examine the association between disease diagnosis and genome-wide autozygosity estimated using runs of homozygosity (ROH) in genome-wide single nucleotide polymorphism arrays. Using data for schizophrenia from the Psychiatric Genomics Consortium (n = 21,868), Keller et al. (2012) estimated that the odds of developing schizophrenia increased by approximately 17% for every additional percent of the genome that is autozygous (β = 16.1, CI(β) = [6.93, 25.7], Z = 3.44, p = 0.0006). Here we describe replication results from 22 independent schizophrenia case-control datasets from the Psychiatric Genomics Consortium (n = 39,830). Using the same ROH calling thresholds and procedures as Keller et al. (2012), we were unable to replicate the significant association between ROH burden and schizophrenia in the independent PGC phase II data, although the effect was in the predicted direction, and the combined (original + replication) dataset yielded an attenuated but significant relationship between Froh and schizophrenia (β = 4.86,CI(β) = [0.90,8.83],Z = 2.40,p = 0.02). Since Keller et al. (2012), several studies reported inconsistent association of ROH burden with complex traits, particularly in case-control data. These conflicting results might suggest that the effects of autozygosity are confounded by various factors, such as socioeconomic status, education, urbanicity, and religiosity, which may be associated with both real inbreeding and the outcome measures of interest.

TidsskriftP L o S Genetics
Udgave nummer10
Sider (fra-til)e1006343
StatusUdgivet - okt. 2016

ID: 49759073