APO E gene and gene-environment effects on plasma lipoprotein-lipid levels
Abstract
Apolipoprotein E (apo E) is important in plasma lipid metabolism and is a component of several plasma lipoprotein-lipid particles. Three major apo E isoforms are encoded by three common alleles at the APO E locus. The E2 allele is associated with lower and the E4 allele with higher total plasma cholesterol and LDL cholesterol levels compared with the E3 allele. Available data generally indicate that APO E2, and possibly E3, genotype individuals reduce plasma total and low-density lipoprotein (LDL) cholesterol levels more than APO E4 individuals with statin therapy. Some evidence also indicates that APO E2 individuals are more likely to respond favorably to gemfibrozil and cholestyramine. On the other hand, it appears that with probucol, APO E4 genotype individuals may improve plasma lipoprotein-lipid profiles more than APO E3 individuals. APO E2 and E3 genotype perimenopausal women appear to improve plasma lipoprotein-lipid profiles more with hormone replacement therapy than APO E4 women. On the other hand, low-fat diet interventions tend to reduce plasma LDL cholesterol and, perhaps, plasma total cholesterol levels more in APO E4 than in APO E2 or E3 individuals. Both cross-sectional and longitudinal studies generally indicate that APO E2 and E3 individuals improve plasma lipoprotein-lipid profiles more with exercise training than APO E4 individuals. Although these data are hardly definitive, they lend strong support for the possibility that in the near future individuals will be directed to what might be their optimal therapy for improving plasma lipoprotein-lipid profiles and cardiovascular disease risk based partially on APO E genotype.
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ApoE4 is associated with a greater lipid response to dietary challenges.
“ApoE4 is associated with a greater lipid response to dietary challenges [58].”
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References 49 · Cited by 118
- Authors
- HAGBERG, J. M., WILUND, K. R., & FERRELL, R. E.
- Affiliations
- University of Pittsburgh (US)
- ORCID
- HAGBERG, JAMES M.
- Venue
- Physiological Genomics
- Publisher
- American Physiological Society
- Published
- 2000-12-18
- Volume
- 4
- Issue
- 2
- Pages
- 101-108
- ISSN
- 1094-8341 (ISSN-L)
- 1531-2267
- OpenAlex
- W2150802827
- Cited by
- 118
- References
- 49
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 1 · 2022: 2 · 2021: 5 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 7 · 2013: 3 · 2012: 4
- FWCI
- 1.44
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Physiological Genomics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01hl045778-06, 5p30dk046204-15)
- National Institute on Aging (AG00268, AG15389, R01AG015389)
- National Heart, Lung, and Blood Institute (HL 45778, HL-39107, R01HL039107)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 46204)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Keywords
- apolipoprotein E, APOE genotype, APOE2, APOE ε4, APOE3, gene-environment interaction, serum lipoproteins, LDL cholesterol, total cholesterol, statin therapy, gemfibrozil, cholestyramine, probucol, hormone replacement therapy, perimenopausal women, low-fat diet, exercise training, lipid-lowering therapy response, cardiovascular risk
- MeSH terms
- Apolipoproteins E, Genotype, Humans, Hyperlipidemias, Lipids, Lipoproteins
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