RFLP alleles at the tyrosine hydroxylase locus: no association found to affective disorders

Psychiatry Res. 1990 Jun;32(3):275-80. doi: 10.1016/0165-1781(90)90032-z.

Abstract

Affective disorders are usually referred to as being inherited multifactorially. The contribution of a gene locus in illnesses displaying multifactorial inheritance may be assessed by searching for associations of alleles to the illness. The tyrosine hydroxylase gene encodes the rate-limiting enzyme in the synthesis of catecholamines and might be a candidate for causing the manic-depressive phenotype. Therefore, we tested 88 patients with affective disorders and 99 healthy control persons for association of restriction fragment length polymorphism (RFLP) alleles at the tyrosine hydroxylase locus. The comparison of allele or genotype frequencies did not reveal any significant differences between the two groups.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Alleles*
  • Bipolar Disorder / diagnosis
  • Bipolar Disorder / genetics*
  • DNA Probes
  • Depressive Disorder / diagnosis
  • Depressive Disorder / genetics*
  • Female
  • Gene Frequency / genetics
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Restriction Fragment Length*
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • DNA Probes
  • Tyrosine 3-Monooxygenase