APOE genotype, eicosapentaenoic acid (EPA) supplementation and n-3 highly unsaturated fatty acid (HUFA) levels in patients with multiple colorectal polyps: A secondary analysis of the seAFOod polyp prevention trial
Author:
Funder
Cancer Research UK
Medical Research Council
National Institute for Health and Care Research
Efficacy and Mechanism Evaluation Programme
Publisher
Elsevier BV
Reference20 articles.
1. The genetic variability of APOE in different human populations and its implications for longevity;Abondio;Genes,2019
2. Alzheimer's disease phenotype based upon the carrier status of the apolipoprotein E ε4 allele;Ji;Brain Pathol.,2023
3. Interaction between BMI and genotype is associated with changes in the plasma long-chain-PUFA response to a fish-oil supplement in healthy participants;Chouinard-Watkins;Am. J. Clin. Nutr.,2015
4. Plasma n-3 fatty acid response to an n-3 fatty acid supplement is modulated by apoE ε4 but not by the common PPAR-alpha L162V polymorphism in men;Plourde;Br. J. Nutr.,2009
5. APOE genotype modifies the plasma oxylipin response to Omega-3 polyunsaturated fatty acid supplementation in healthy individuals;Saleh;Front. Nutr.,2021
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