# Meat Consumption and Cognitive Health by APOE Genotype

**Authors:** Jakob Norgren, Adrián Carballo-Casla, Giulia Grande, Anne Börjesson-Hanson, Hong Xu, Maria Eriksdotter, Erika J. Laukka, Sara Garcia-Ptacek

PMC · DOI: 10.1001/jamanetworkopen.2026.6489 · 2026-03-19

## TL;DR

Eating more meat may help protect cognitive health in older adults with specific APOE gene variants linked to Alzheimer's risk.

## Contribution

The study identifies a genotype-specific dietary effect of meat consumption on cognitive decline and dementia risk.

## Key findings

- Higher meat consumption was linked to slower cognitive decline in APOE ε3/ε4 and ε4/ε4 individuals.
- APOE ε3/ε4 and ε4/ε4 carriers with high meat intake had a 55% lower dementia risk compared to low consumers.
- No cognitive benefits of meat were observed in individuals with other APOE genotypes.

## Abstract

This cohort study investigates the association of meat consumption with risk of cognitive decline and dementia among older adults with APOE genotypes ε3/ε4 and ε4/ε4.

Is higher meat consumption associated with better cognitive health among individuals with APOE genotypes ε3/ε4 and ε4/ε4, and does this association differ from that observed in other genotypes?

In this cohort study among 2157 older adults without dementia, higher total meat consumption was associated with slower cognitive decline and a reduced dementia risk among older adults with APOE ε3/ε4 and ε4/ε4 genotypes. Interactions by APOE genotype were observed for trajectories of global cognition and episodic memory.

These findings suggest that higher meat consumption than conventionally recommended may be associated with benefits in a genetically defined subgroup comprising approximately one-quarter of the global population.

The apolipoprotein E (APOE) ε4 allele increases Alzheimer disease risk. Understanding genotype-specific dietary needs could inform more personalized prevention strategies.

To test the hypothesis that higher meat consumption may be associated with cognitive health benefits in individuals with APOE genotypes ε3/ε4 and ε4/ε4 (APOE34/44) and to examine whether this association differs from that in other genotypes.

This population-based cohort study used panel data analyses conducted in January 2025 to January 2026 over 15 years of follow-up in the Swedish National Study on Aging and Care–Kungsholmen (SNAC-K), using strategies aligned with causal inference principles. Recruitment was done in 2001 to 2004 among adults without dementia aged 60 years or older.

The primary exposure was total meat consumption in grams per total kilocalories assessed via validated food frequency questionnaires. The secondary exposure was the ratio of processed to total meat.

Global cognitive trajectory, measured as change in z score per 10 years, was analyzed by linear regression. Incident dementia was analyzed using Fine and Gray subdistribution hazard ratios (sHRs), treating nondementia death as a competing risk.

Among 2157 older adults without dementia (mean [SD] age 71.2 [9.2] years; 1337 female [62.0%]), 1680 participants had longitudinal cognition data and 569 participants (26.4%) had APOE34/44 genotypes. During follow-up, 296 participants developed dementia and 690 died without dementia. Among participants with APOE34/44 genotypes, higher total meat consumption (top vs bottom quintile) was associated with better cognitive trajectories (β = 0.32; 95% CI, 0.07 to 0.56; P = .01) and reduced dementia risk (sHR, 0.45; 95% CI, 0.21 to 0.95; P = .04). No associations were found in participants with APOE22/23/24/33 genotypes (cognitive trajectory: β = –0.11; 95% CI, –0.27 to 0.06; P = .20; dementia: sHR, 0.95; 95% CI, 0.57 to 1.61; P = .86). P values for APOE interaction were .004 for cognition and .10 for dementia. In the top quintile of meat consumption, dementia risk and cognitive decline were similar between APOE strata. A higher ratio of processed to total meat was unfavorably associated with dementia (sHR, 1.14; 95% CI, 1.01 to 1.29; P = .04), showing no APOE interaction and no substantial difference between unprocessed red meat and poultry. Post hoc analyses suggested concordant APOE interaction for all-cause mortality (unprocessed meat exposure, APOE34/44: HR, 0.85; 95% CI, 0.73 to 0.99; P = 0.04; P for interaction = .03).

In this study, higher meat consumption was associated with better cognitive trajectories and lower dementia risk among individuals with APOE34/44 genotypes. The expected cognitive disadvantage among individuals with APOE34/44 genotypes was not observed at high meat consumption, suggesting clinical and public health relevance.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348]
- **Diseases:** Alzheimer disease (MONDO:0004975), dementia (MONDO:0001627)

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}
- **Diseases:** Dementia (MESH:D003704), chronic (MESH:D002908), Alzheimer (MESH:D000544), hypertension (MESH:D006973), dyslipidemia (MESH:D050171), obesity (MESH:D009765), depression (MESH:D003866), death (MESH:D003643), Mental Disorders (MESH:D001523), anemia (MESH:D000740), cognitive decline (MESH:D003072), Cardiovascular (MESH:D002318), parasitic infections (MESH:D010272), diabetes (MESH:D003920)
- **Chemicals:** PUFA (MESH:D005231), carbohydrate (MESH:D002241), vitamin B12 (MESH:D014805), SFA (-), cholesterol (MESH:D002784), alcohol (MESH:D000438), fat (MESH:D005223)
- **Species:** Homo sapiens (human, species) [taxon 9606], Pan troglodytes (chimpanzee, species) [taxon 9598]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13003371/full.md

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Source: https://tomesphere.com/paper/PMC13003371