Interactions between dietary patterns and genetic factors in relation to incident dementia among 70-year-olds

Eur J Nutr. 2022 Mar;61(2):871-884. doi: 10.1007/s00394-021-02688-9. Epub 2021 Oct 10.

Abstract

Purpose: To investigate potential interactions between dietary patterns and genetic factors modulating risk for Alzheimer's disease (AD) in relation to incident dementia.

Methods: Data were derived from the population-based Gothenburg H70 Birth Cohort Studies in Sweden, including 602 dementia-free 70-year-olds (examined 1992-93, or 2000-02; 64% women) followed for incident dementia until 2016. Two factors from a reduced rank regression analysis were translated into dietary patterns, one healthy (e.g., vegetables, fruit, and fish) and one western (e.g., red meat, refined cereals, and full-fat dairy products). Genetic risk was determined by APOE ε4 status and non-APOE AD-polygenic risk scores (AD-PRSs). Gene-diet interactions in relation to incident dementia were analysed with Cox regression models. The interaction p value threshold was < 0.1.

Results: There were interactions between the dietary patterns and APOE ε4 status in relation to incident dementia (interaction p value threshold of < 0.1), while no evidence of interactions were found between the dietary patterns and the AD-PRSs. Those with higher adherence to a healthy dietary pattern had a reduced risk of dementia among ε4 non-carriers (HR: 0.77; 95% CI: 0.61; 0.98), but not among ε4 carriers (HR: 0.86; CI: 0.63; 1.18). Those with a higher adherence to the western dietary pattern had an increased risk of dementia among ε4 carriers (HR: 1.37; 95% CI: 1.05; 1.78), while no association was observed among ε4 non-carriers (HR: 0.99; CI: 0.81; 1.21).

Conclusions: The results of this study suggest that there is an interplay between dietary patterns and APOE ε4 status in relation to incident dementia.

Keywords: Apolipoprotein E genotype; Dementia; Dietary pattern; Nutrition; Polygenic risk score.

MeSH terms

  • Alzheimer Disease* / epidemiology
  • Alzheimer Disease* / genetics
  • Animals
  • Apolipoprotein E4* / genetics
  • Female
  • Genotype
  • Heterozygote
  • Humans
  • Male
  • Proportional Hazards Models
  • Risk Factors

Substances

  • Apolipoprotein E4

Grants and funding