Tyrosine hydroxylase gene in linkage disequilibrium with mood disorders

Mol Psychiatry. 1998 Mar;3(2):169-74. doi: 10.1038/sj.mp.4000373.

Abstract

We studied tyrosine hydroxylase (TH) gene variants in mood disorders using linkage disequilibrium techniques. One hundred and forty-five inpatients affected by bipolar (n = 88) and unipolar (n = 57) disorders, and 84 healthy controls, were typed for TH variants using polymerase chain reaction (PCR) amplification. TH was associated with mood disorder, with all affected subjects presenting an excess of TH*2 allele (chi 2 = 8.30, d.f. = 1; P = 0.004) and lack of the TH*1 allele (chi 2 = 6.90, d.f. = 1, P = 0.009). Linkage disequilibrium analyses confirmed the association. Our results suggest a moderate linkage disequilibrium of TH variants with mood disorders.

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Alleles
  • Bipolar Disorder / epidemiology
  • Bipolar Disorder / genetics
  • Chromosomes, Human, Pair 11 / genetics*
  • DNA / genetics
  • DNA Mutational Analysis
  • Depressive Disorder / epidemiology
  • Depressive Disorder / genetics
  • Female
  • Genotype
  • Humans
  • Italy / epidemiology
  • Linkage Disequilibrium / genetics*
  • Male
  • Middle Aged
  • Mood Disorders / epidemiology
  • Mood Disorders / genetics*
  • Nerve Tissue Proteins / genetics*
  • Polymerase Chain Reaction
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Nerve Tissue Proteins
  • DNA
  • Tyrosine 3-Monooxygenase