4.7 Article

Apolipoprotein E epsilon 4 genotype and a physically active lifestyle in late life: analysis of gene-environment interaction for the risk of dementia and Alzheimer's disease dementia

Journal

PSYCHOLOGICAL MEDICINE
Volume 44, Issue 6, Pages 1319-1329

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291713001918

Keywords

Additive interaction; apolipoprotein E epsilon 4; dementia; gene-environment interaction; lifestyle; physical activity

Funding

  1. German Federal Ministry of Education and Research [KND 01GI0102, 01GI0420, 01GI0422, 01GI0423, 01GI0429, 01GI0431, 01GI0433, 01GI0434, KNDD 01GI0710, 01GI0711, 01GI0712, 01GI0713, 01GI0714, 01GI0715, 01GI0716, 01ET1006B]
  2. German Research Foundation [Lu 1730/1-1]

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Background. As physical activity may modify the effect of the apolipoprotein E (APOE) epsilon 4 allele on the risk of dementia and Alzheimer's disease (AD) dementia, we tested for such a gene-environment interaction in a sample of general practice patients aged 575 years. Method. Data were derived from follow-up waves I-IV of the longitudinal German study on Ageing, Cognition and Dementia in Primary Care Patients (AgeCoDe). The Kaplan-Meier survival method was used to estimate dementiaand AD-free survival times. Multivariable Cox regression was used to assess individual associations of APOE epsilon 4 and physical activity with risk for dementia and AD, controlling for covariates. We tested for gene-environment interaction by calculating three indices of additive interaction. Results. Among the randomly selected sample of 6619 patients, 3327 (50.3%) individuals participated in the study at baseline and 2810 (42.5%) at follow-up I. Of the 2492 patients without dementia included at follow-up I, 278 developed dementia (184 AD) over the subsequent follow-up interval of 4.5 years. The presence of the APOE epsilon 4 allele significantly increased and higher physical activity significantly decreased risk for dementia and AD. The co-presence of APOE epsilon 4 with low physical activity was associated with higher risk for dementia and AD and shorter dementia-and AD-free survival time than the presence of APOE epsilon 4 or low physical activity alone. Indices of interaction indicated no significant interaction between low physical activity and the APOE epsilon 4 allele for general dementia risk, but a possible additive interaction for AD risk. Conclusions. Physical activity even in late life may be effective in reducing conversion to dementia and AD or in delaying the onset of clinical manifestations. APOE epsilon 4 carriers may particularly benefit from increasing physical activity with regard to their risk for AD.

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