Ankle-to-brachial index and dementia: the Honolulu-Asia Aging Study

Danielle Laurin1, Kamal H Masaki, Lon R White

  • 1Laval University Geriatrics Research Unit, Centre de recherche du CHA, and Faculty of Pharmacy, Laval University, Quebec City, Quebec, Canada.

Circulation
|October 31, 2007
PubMed

Insights

A low ankle-brachial index (ABI), indicating peripheral artery disease, is linked to a higher risk of dementia, especially vascular dementia. This association is particularly noted in individuals with the apolipoprotein E epsilon4 gene variant.

Area of Science:

  • Neurology
  • Cardiology
  • Gerontology

Background:

  • The ankle-brachial index (ABI) is a noninvasive measure for peripheral arterial disease (PAD).
  • PAD and cardiovascular disease share common risk factors and mortality correlations.
  • Vascular factors are implicated in dementia pathogenesis.

Purpose of the Study:

  • To investigate the association between ABI and the incidence of dementia.
  • To explore the relationship between ABI and specific dementia subtypes, including Alzheimer's disease and vascular dementia.

Main Methods:

  • Utilized data from the Honolulu-Asia Aging Study (HAAS), a prospective cohort study.
  • Included 2588 Japanese American men, free of dementia at baseline, with ABI measurements.
  • Employed Cox proportional-hazards models, adjusting for multiple covariates, to assess dementia risk.

Main Results:

  • A low ABI was significantly associated with an increased risk of overall dementia and vascular dementia.
  • ABI showed a weaker association with Alzheimer's disease, particularly in apolipoprotein E epsilon4 carriers.
  • Hazard ratios indicated a 66% increased risk for dementia and a 125% increased risk for vascular dementia with low ABI.

Conclusions:

  • ABI, a marker of atherosclerosis, is associated with the incidence of dementia, vascular dementia, and Alzheimer's disease.
  • The association between ABI and dementia subtypes is more pronounced in individuals carrying the apolipoprotein E epsilon4 allele.
Abstract

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