Estimating the genetic variance of major depressive disorder due to all single nucleotide polymorphisms

Biol Psychiatry. 2012 Oct 15;72(8):707-9. doi: 10.1016/j.biopsych.2012.03.011. Epub 2012 Apr 19.

Abstract

Genome-wide association studies of psychiatric disorders have been criticized for their lack of explaining a considerable proportion of the heritability established in twin and family studies. Genome-wide association studies of major depressive disorder in particular have so far been unsuccessful in detecting genome-wide significant single nucleotide polymorphisms (SNPs). Using two recently proposed methods designed to estimate the heritability of a phenotype that is attributable to genome-wide SNPs, we show that SNPs on current platforms contain substantial information concerning the additive genetic variance of major depressive disorder. To assess the consistency of these two methods, we analyzed four other complex phenotypes from different domains. The pattern of results is consistent with estimates of heritability obtained in twin studies carried out in the same population.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Depressive Disorder, Major / diagnosis
  • Depressive Disorder, Major / genetics*
  • Fasting
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Variation / genetics*
  • Genome-Wide Association Study*
  • Genotype
  • Glucose
  • Humans
  • Male
  • Models, Statistical
  • Netherlands
  • Polymorphism, Single Nucleotide / genetics*
  • Smoking / genetics
  • Twin Studies as Topic

Substances

  • Glucose