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Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study

The risk of dementia and Alzheimer's disease (AD) probably results from an interaction between genetic and environmental factors. The aim of this study was to investigate the effects and putative interactions between the apoE ε4 allele and lifestyle related risk factors for dementia and AD. Par...

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Autores principales: Kivipelto, Miia, Rovio, Suvi, Ngandu, Tiia, Kåreholt, Ingemar, Eskelinen, Marjo, Winblad, Bengt, Hachinski, Vladimir, Cedazo-Minguez, Angel, Soininen, Hilkka, Tuomilehto, Jaakko, Nissinen, Aulikki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828889/
https://www.ncbi.nlm.nih.gov/pubmed/18318693
http://dx.doi.org/10.1111/j.1582-4934.2008.00296.x
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author Kivipelto, Miia
Rovio, Suvi
Ngandu, Tiia
Kåreholt, Ingemar
Eskelinen, Marjo
Winblad, Bengt
Hachinski, Vladimir
Cedazo-Minguez, Angel
Soininen, Hilkka
Tuomilehto, Jaakko
Nissinen, Aulikki
author_facet Kivipelto, Miia
Rovio, Suvi
Ngandu, Tiia
Kåreholt, Ingemar
Eskelinen, Marjo
Winblad, Bengt
Hachinski, Vladimir
Cedazo-Minguez, Angel
Soininen, Hilkka
Tuomilehto, Jaakko
Nissinen, Aulikki
author_sort Kivipelto, Miia
collection PubMed
description The risk of dementia and Alzheimer's disease (AD) probably results from an interaction between genetic and environmental factors. The aim of this study was to investigate the effects and putative interactions between the apoE ε4 allele and lifestyle related risk factors for dementia and AD. Participants of the Cardiovascular Risk Factors, Aging, and Dementia (CAIDE) study were derived from random, population-based samples previously studied in 1972, 1977, 1982 or 1987. After an average follow-up of 21 years, 1449 individuals (72.5%) aged 65–79 years were re-examined in 1998. The apoE ε4 allele was an independent risk factor for dementia/AD even after adjustments for sociodemographic, lifestyle and vascular factors (odds ratio [OR]= 2.83, 95% confidence interval [CI]ε1.61–4.97). Physical inactivity, alcohol drinking and smoking increased the risk of dementia/AD particularly among the apoE ε4 carriers. Furthermore, low–moderate intake of polyunsaturated, and moderate–high intake of saturated fats were associated with an increased risk of dementia/AD more pronouncedly among apoE ε4 carriers. Composite effect of the lifestyle factors was particularly seen among the ε4 carriers (OR = 11.42, 95% CI = 1.94–67.07 in the 4(th) quartile). Physical inactivity, dietary fat intake, alcohol drinking and smoking at midlife are associated with the risk of dementia and AD, especially among the apoE ε4 carriers. The apoE ε4 carriers may be more vulnerable to environmental factors, and thus, lifestyle interventions may greatly modify dementia risk particularly among the genetically susceptible individuals.
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spelling pubmed-38288892015-04-27 Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study Kivipelto, Miia Rovio, Suvi Ngandu, Tiia Kåreholt, Ingemar Eskelinen, Marjo Winblad, Bengt Hachinski, Vladimir Cedazo-Minguez, Angel Soininen, Hilkka Tuomilehto, Jaakko Nissinen, Aulikki J Cell Mol Med Articles The risk of dementia and Alzheimer's disease (AD) probably results from an interaction between genetic and environmental factors. The aim of this study was to investigate the effects and putative interactions between the apoE ε4 allele and lifestyle related risk factors for dementia and AD. Participants of the Cardiovascular Risk Factors, Aging, and Dementia (CAIDE) study were derived from random, population-based samples previously studied in 1972, 1977, 1982 or 1987. After an average follow-up of 21 years, 1449 individuals (72.5%) aged 65–79 years were re-examined in 1998. The apoE ε4 allele was an independent risk factor for dementia/AD even after adjustments for sociodemographic, lifestyle and vascular factors (odds ratio [OR]= 2.83, 95% confidence interval [CI]ε1.61–4.97). Physical inactivity, alcohol drinking and smoking increased the risk of dementia/AD particularly among the apoE ε4 carriers. Furthermore, low–moderate intake of polyunsaturated, and moderate–high intake of saturated fats were associated with an increased risk of dementia/AD more pronouncedly among apoE ε4 carriers. Composite effect of the lifestyle factors was particularly seen among the ε4 carriers (OR = 11.42, 95% CI = 1.94–67.07 in the 4(th) quartile). Physical inactivity, dietary fat intake, alcohol drinking and smoking at midlife are associated with the risk of dementia and AD, especially among the apoE ε4 carriers. The apoE ε4 carriers may be more vulnerable to environmental factors, and thus, lifestyle interventions may greatly modify dementia risk particularly among the genetically susceptible individuals. Blackwell Publishing Ltd 2008-12 2008-03-04 /pmc/articles/PMC3828889/ /pubmed/18318693 http://dx.doi.org/10.1111/j.1582-4934.2008.00296.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Kivipelto, Miia
Rovio, Suvi
Ngandu, Tiia
Kåreholt, Ingemar
Eskelinen, Marjo
Winblad, Bengt
Hachinski, Vladimir
Cedazo-Minguez, Angel
Soininen, Hilkka
Tuomilehto, Jaakko
Nissinen, Aulikki
Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title_full Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title_fullStr Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title_full_unstemmed Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title_short Apolipoprotein E ε4 magnifies lifestyle risks for dementia: a population-based study
title_sort apolipoprotein e ε4 magnifies lifestyle risks for dementia: a population-based study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828889/
https://www.ncbi.nlm.nih.gov/pubmed/18318693
http://dx.doi.org/10.1111/j.1582-4934.2008.00296.x
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