Apolipoprotein E epsilon 4 allele and Japanese late-onset depressive disorders

Biol Psychiatry. 1999 Feb 1;45(3):308-12. doi: 10.1016/s0006-3223(97)00548-9.

Abstract

Background: Several studies have suggested that late-onset depressive disorder (LOD) and the apolipoprotein E (Apo E) epsilon 4 allele are associated with dementia, respectively. The Apo E polymorphism is significantly heterogeneous among races. We hypothesized that the Apo E epsilon 4 allele frequency is elevated in Japanese LOD.

Methods: The Apo E genotype was studied in 134 patients (male, 53; female, 81) with early-/late-onset depressive disorder and 105 healthy normal controls (male, 41; female, 64). The patients were subdivided into those with early onset and late onset using 45 and 50 years as the cutoff ages. All the subjects were Japanese.

Results: There was statistically no difference between normal control subjects and patients with depressive disorders in Apo E genotype or allele frequency. There was statistically no difference in the age of onset of depressive disorders according to the Apo E genotype. There was no relation between the age of onset of depressive disorder and the number of epsilon 4 alleles the patient had. There was also no association between early-/late-onset depressive disorder and the Apo E genotype or allele frequency.

Conclusions: Our results suggest that there is no association between the Apo E epsilon 4 allele and Japanese LOD.

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Alleles
  • Analysis of Variance
  • Apolipoproteins E / genetics*
  • Case-Control Studies
  • Chi-Square Distribution
  • Dementia / ethnology
  • Dementia / genetics
  • Depressive Disorder / classification
  • Depressive Disorder / ethnology
  • Depressive Disorder / genetics*
  • Female
  • Genotype
  • Humans
  • Japan / ethnology
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Survival Analysis

Substances

  • Apolipoproteins E