Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

J Med Genet. 2006 Jul;43(7):563-7. doi: 10.1136/jmg.2005.035345. Epub 2005 Oct 14.

Abstract

Background: Schizophrenia shows substantial clinical heterogeneity. One common important clinical variable in presentation is the occurrence of episodes of major depression.

Methods: We undertook analyses in an attempt to detect loci that influence susceptibility to, or modify the clinical expression of, schizophrenia according to the occurrence of episodes of major depression. We used a logistic regression framework in which lifetime presence/absence of major depression was entered as a covariate in the linkage analysis of our UK schizophrenia affected sibling pair series (168 affected sibling pairs typed for a 10 cM map of microsatellite markers).

Results: Inclusion of presence/absence of depression as a covariate detected a genome wide significant linkage signal on chromosome 4q28.3 at 130.7 cM (LOD = 4.59; p = 0.038; increase in maximum LOD over univariate analysis (ILOD) = 3.62). Inclusion of the depression covariate also showed suggestive evidence of linkage on 20q11.21 (LOD = 4.10; expected to occur by chance 0.093 times per genome scan, ILOD = 2.83).

Conclusions: Our findings identify loci that may harbour genes that play a role in susceptibility to, or modify the risk of, episodes of major depression in people with schizophrenia.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 4*
  • Conditioning, Psychological
  • Depressive Disorder / genetics*
  • Depressive Disorder / psychology
  • Genetic Predisposition to Disease
  • Genome, Human*
  • Genotype
  • Humans
  • Ireland
  • Mood Disorders / genetics
  • Schizophrenia / genetics*
  • Schizophrenic Psychology
  • Siblings
  • Syndrome
  • United Kingdom