Genetic linkage of region containing the CREB1 gene to depressive disorders in families with recurrent, early-onset, major depression: a re-analysis and confirmation of sex-specific effect

Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):10-6. doi: 10.1002/ajmg.b.30987.

Abstract

A previously published model-free linkage analysis of chromosome 2q33-35, highlighted by previous case-control studies and supported by within-family analyses employing the transmission disequilibrium test, revealed evidence of sex-specific linkage of the CREB1-containing region of 2q to unipolar mood disorders among women in 81 recurrent, early-onset, major depressive disorder (RE-MDD) families. Since it has been reported that the LODPAL program from S.A.G.E. v.4.0 used to conduct this previous linkage analysis suffers from an increased type I error rate that is exacerbated by covariates such as sex, we re-analyzed the evidence for this sex-specific linkage result using a simulation approach to estimate the empirical significance of our previous results. The results continue to support sex-specific linkage of the CREB1 region to mood disorders among women from families with RE-MDD. Moreover, these results have been supported by a host of additional published findings that implicate sequence variations in CREB1 in the sex-dependent development of syndromic mood disorders, as well as related clinical features and disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Age of Onset
  • Chromosomes, Human, Pair 2
  • Cyclic AMP Response Element-Binding Protein / genetics*
  • Depression / genetics*
  • Female
  • Genetic Linkage*
  • Humans
  • Male
  • Recurrence
  • Sex Factors*

Substances

  • CREB1 protein, human
  • Cyclic AMP Response Element-Binding Protein