Does overall diet in midlife predict future aging phenotypes? A cohort study
- PMID: 23582933
- PMCID: PMC3743043
- DOI: 10.1016/j.amjmed.2012.10.028
Does overall diet in midlife predict future aging phenotypes? A cohort study
Erratum in
- Am J Med. 2013 Jun;126(6):e25
Abstract
Background: The impact of diet on specific age-related diseases has been studied extensively, but few investigations have adopted a more holistic approach to determine the association of diet with overall health at older ages. We examined whether diet, assessed in midlife, using dietary patterns and adherence to the Alternative Healthy Eating Index (AHEI), is associated with aging phenotypes, identified after a mean 16-year follow-up.
Methods: Data were drawn from the Whitehall II cohort study of 5350 adults (age 51.3±5.3 years, 29.4% women). Diet was assessed at baseline (1991-1993). Mortality, chronic diseases, and functioning were ascertained from hospital data, register linkage, and screenings every 5 years and were used to create 5 outcomes at follow-up: ideal aging (free of chronic conditions and high performance in physical, mental, and cognitive functioning tests; 4%), nonfatal cardiovascular event (12.7%), cardiovascular death (2.8%), noncardiovascular death (7.3%), [corrected] and normal aging (73.2%).
Results: Low adherence to the AHEI was associated with an increased risk of cardiovascular and noncardiovascular death. In addition, participants with a "Western-type" diet (characterized by high intakes of fried and sweet food, processed food and red meat, refined grains, and high-fat dairy products) had lower odds of ideal aging (odds ratio for top vs bottom tertile: 0.58; 95% confidence interval, 0.36-0.94; P=.02), independently of other health behaviors.
Conclusions: By considering healthy aging as a composite of cardiovascular, metabolic, musculoskeletal, respiratory, mental, and cognitive function, the present study offers a new perspective on the impact of diet on aging phenotypes.
Copyright © 2013 Elsevier Inc. All rights reserved.
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- RG/13/2/30098/BHF_/British Heart Foundation/United Kingdom
- R01 HL036310/HL/NHLBI NIH HHS/United States
- G19/35/MRC_/Medical Research Council/United Kingdom
- G0100222/MRC_/Medical Research Council/United Kingdom
- G0902037/MRC_/Medical Research Council/United Kingdom
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- HS06516/HS/AHRQ HHS/United States
- R01AG013196/AG/NIA NIH HHS/United States
- RG/07/008/23674/BHF_/British Heart Foundation/United Kingdom
- R01AG034454/AG/NIA NIH HHS/United States
- R01HL036310/HL/NHLBI NIH HHS/United States
- G8802774/MRC_/Medical Research Council/United Kingdom
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