Beneficial Effect of Societal Factors on APOE-ε2 and ε4 Carriers' Brain Health: A Systematic Review

J Gerontol A Biol Sci Med Sci. 2024 Feb 1;79(2):glad237. doi: 10.1093/gerona/glad237.

Abstract

Background: Apolipoprotein-E (APOE) ε4 and ε2 are the most prevalent risk-increasing and risk-reducing genetic predictors of Alzheimer's disease, respectively. However, the extent to which societal factors can reduce the harmful impact of APOE-ε4 and enhance the beneficial impact of APOE-ε2 on brain health has not yet been examined systematically.

Methods: To fill this gap, we conducted a systematic review searching for studies in MEDLINE, Embase, PsycINFO, and Scopus until June 2023, that included: (a) 1 of 5 social determinants of health (SDH) identified by Healthy People 2030, (b) APOE-ε2 or APOE-ε4 allele carriers, (c) cognitive or brain-biomarker outcomes, and (d) studies with an analysis of how APOE-ε2 and/ or APOE-ε4 carriers differ on outcomes when exposed to SDH.

Results: From 14 076 articles retrieved, 124 met the inclusion criteria. In most of the studies, exposure to favorable SDH reduced APOE-ε4's detrimental effect and enhanced APOE-ε2's beneficial effect on cognitive and brain-biomarker outcomes (cognition: 70.5%, n: 74/105; brain-biomarkers: 71.4%, n: 20/28). A similar pattern of results emerged in each of the 5 Healthy People 2030 SDH categories, where finishing high school, having resources to satisfy basic needs, less air pollution, less negative external stimuli that can generate stress (eg, negative age stereotypes), and exposure to multiple favorable SDH were associated with better cognitive and brain health among APOE-ε4 and APOE-ε2 carriers.

Conclusions: Societal factors can reduce the harmful impact of APOE-ε4 and enhance the beneficial impact of APOE-ε2 on cognitive outcomes. This suggests that plans to reduce dementia should include community-level policies promoting favorable SDH.

Keywords: Apolipoprotein E4; Cognitive impairment; Cognitive reserve; Health disparity; Minority and vulnerable populations.

Publication types

  • Systematic Review

MeSH terms

  • Alleles
  • Alzheimer Disease* / genetics
  • Apolipoprotein E2 / genetics
  • Apolipoprotein E4 / genetics
  • Apolipoproteins E* / genetics
  • Biomarkers
  • Brain
  • Genotype
  • Humans

Substances

  • Apolipoprotein E2
  • Apolipoprotein E4
  • Apolipoproteins E
  • Biomarkers
  • ApoE protein, human