Autosomal recessive inheritance of affective disorders in families of responders to lithium prophylaxis?

J Affect Disord. 1997 Jul;44(2-3):153-7. doi: 10.1016/s0165-0327(97)00042-6.

Abstract

In this paper we report the results of a study of the mode of inheritance in affective disorders responsive to lithium. Earlier we described a series of 71 families in which the genetic transmission was compatible with a single-gene model. We have now carried out an independent replication study on 25 newly recruited families in a different geographical location. The autosomal recessive model from our original study could not be rejected with the new data. In a subsequent analysis of the pooled sample of 96 families, a recessive model with a common predisposing allele (q = 0.16) and sex-specific penetrance (0.35 in males, 0.66 in females) fitted the data best. On the other hand, X-chromosome and polygenic models could be rejected. The finding of a major-gene effect represents a specific hypothesis that can be tested by molecular genetic techniques.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Antidepressive Agents / therapeutic use*
  • Chromosome Aberrations
  • Chromosome Disorders
  • Female
  • Humans
  • Lithium / therapeutic use*
  • Male
  • Middle Aged
  • Mood Disorders / genetics*
  • Mood Disorders / prevention & control*
  • Mood Disorders / psychology
  • X Chromosome

Substances

  • Antidepressive Agents
  • Lithium