Genetic polymorphisms in older subjects with vascular or Alzheimer's dementia

Acta Neurol Scand. 2001 May;103(5):304-8. doi: 10.1034/j.1600-0404.2001.103005304.x.

Abstract

Objectives: Paraoxonase, angiotensin-converting enzyme (ACE), methylenetetrahydrofolate reductase (MTHFR), and apo E gene polymorphisms were evaluated in older patients with vascular dementia (VD) or late-onset Alzheimer's disease (LOAD).

Material and methods: Sixty patients with VD, 45 patients with LOAD, and 54 non-demented controls were compared.

Results: No differences in the distribution of paraoxonase, ACE, and MTHFR polymorphisms were found. The overall frequency of apo E epsilon4 allele was "low"; epsilon4 allele was more frequent in LOAD (17.5%) and VD (13.3%) compared with controls (9.2%), but the difference was not statistically significant.

Conclusion: Paraoxonase, ACE, and MTHFR polymorphisms were not associated with VD or LOAD; these common polymorphisms might have a marginal role in the pathogenesis of dementia in older subjects. In spite of a "low" frequency of the apo E epsilon4 allele in our sample, the frequency of epsilon4 allele was about double in LOAD compared with controls.

MeSH terms

  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / genetics*
  • Apolipoproteins E / genetics
  • Aryldialkylphosphatase
  • Dementia, Vascular / genetics*
  • Esterases / genetics
  • Female
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Oxidoreductases Acting on CH-NH Group Donors / genetics
  • Peptidyl-Dipeptidase A / genetics
  • Polymorphism, Genetic*

Substances

  • Apolipoproteins E
  • Oxidoreductases Acting on CH-NH Group Donors
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Esterases
  • Aryldialkylphosphatase
  • Peptidyl-Dipeptidase A