Skip to content
Open access

Nutritional Status and Cognition in Older Adults: Modification by Apolipoprotein E ε4

Sep 2026 · Nutrients · Vol 18, pp. 3217 · 0 citations · 39 references
Medicine

TL;DR

Better nutritional status was associated with better global cognition, predominantly in APOE4 non-carriers, and hypothesis-generating findings require confirmation in larger longitudinal and interventional studies.

Abstract

Background: Malnutrition is a modifiable risk factor for late-life cognitive decline, but whether its cognitive correlates vary by genetic risk is unclear. We examined whether the apolipoprotein E ε4 allele (APOE4) modifies associations of the Mini-Nutritional Assessment (MNA) and its subscales with global cognition. Methods: In this cross-sectional analysis of 196 non-demented older Korean adults from the General Lifestyle and Alzheimer’s Disease (GLAD) cohort, multiple linear regression tested associations of MNA total (MNA-T), screening (MNA-S), and assessment (MNA-A) scores with the CERAD total score (TS), including MNA × APOE4 interactions. Exploratory analyses examined one representative item per a priori nutritional domain. Results: After adjustment, MNA-T (p = 0.006) and MNA-A (p = 0.003), but not MNA-S (p = 0.065), were associated with TS. APOE4 carrier status modified these associations (interaction p = 0.005 and 0.007, respectively); associations were evident in non-carriers but not in carriers, an underpowered subgroup (n = 40). Among the domain-representative items, only self-rated health survived Bonferroni correction (p = 0.006); protein intake (p = 0.025) and calf circumference (p = 0.043) showed nominal associations only. Conclusions: Better nutritional status was associated with better global cognition, predominantly in APOE4 non-carriers. These hypothesis-generating findings require confirmation in larger longitudinal and interventional studies.

Read PDF

Similar papers

Open access Oct 2026

Allostatic Load Indices and Cognition Among Older Adults: The Moderating Role of Apolipoprotein ε4 Genotype on Metabolic Burden

Objective: Allostatic Load (AL), an index of multisystem biological dysregulation, is linked with adverse cognitive outcomes. The Apolipoprotein E-ε4 (APOE-ε4) genetic variant is associated with an accelerated cognitive decline and Alzheimer’s disease. This study investigates the association between AL indices (nutri...

Mubarick Saeed, Charles F. Murchison, D. Geldmacher et al. · 0 citations
Open access Oct 2026

APOE4 allele modifies the effect of lifestyle interventions on cognition

The apolipoprotein E ε4 allele (APOE4) is the main genetic risk factor for incidence and earlier onset of dementia, and APOE4 carriers are thus considered a key target group for dementia risk reduction. APOE4 carriership also impacts the association between lifestyle and cognitive decline. Our meta-analysis inves...

J. Lehtisalo, Ari Solomon, E. Levälahti et al. · 0 citations
Open access Sep 2026

Serum biomarkers, modifiable risk factors, cognition, and processing speed in older adults.

Serum creatinine levels and depressive symptoms were independently associated with global cognition and processing speed and diabetes was independently associated with processing speed.

Chia-Te Chen, Fong-Ping Tang, Chia-Hao Fan et al. · 0 citations
Open access Sep 2026

Amyloid Beta Biomarkers and Their Association with Cognitive Impairment Across Vitamin D Strata: A Cross-Sectional Study in an Older Adult South Indian Population

Introduction: Vitamin D status has been investigated as a modifiable risk factor with cognitive decline. However, studies pertaining to this remain inconsistent across populations, and there are fewer studies associating vitamin D status, cognitive decline, amyloid markers and oxidative stress markers in older adults....

Rajalakshmi Ramashetty, Rimshia Naaz, R. M. et al. · 0 citations
Aug 2026

Age-Dependent and APOE-Modified Associations Between Vascular Risk Factor Patterns and Cognitive Function: A Latent Class Analysis of 44,879 NACC Participants.

Attenuated associations in older-old adults may reflect survivor bias, while stronger associations in APOE ε4 carriers are consistent with gene-environment interactions, which are consistent with gene-environment interactions.

Yang Kong, Xian Li, Rui-Qian Guan et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.