Cited by 112Lipoproteins and Cardiovascular HealthLipid metabolism and disordersParaoxonase enzyme and polymorphisms

Reciprocal effects of apolipoprotein E alleles (ε2 AND ε4) on plasma lipid levels in normolipidemic subjects

Eto, M., Watanabe, K., Ishii, K.·1986·Clinical Genetics

Abstract

A significantly lower frequency of the ε2 allele and a significantly higher frequency of the ε3 allele were found in the normolipidemic Japanese population than those in the normolipidemic Caucasian populations. We have compared plasma lipid variables among the apolipoprotein (apo) E phenotype groups and estimated the average effects of the three common alleles (ε2, ε3 and ε4) on plasma lipid levels in normolipidemic subjects. Plasma triglyceride (TG), very low density lipoprotein (VLDL)‐TG, VLDL‐cholesterol (C) and apo E levels were high in the apo E3/2 group, intermediate in the apo E3/3 group and low in the apo E4/3 group, whereas plasma total cholesterol (TC), low density lipoprotein (LDL)‐C and high density lipoprotein (HDL)‐C levels were low in the apo E3/2 group, intermediate in the apo E3/3 group and high in the apo E4/3 group. Furthermore, the ε2 allele had an effect to increase the TG, VLDL‐TG, VLDL‐C and apo E levels and decrease the TC, LDL‐C and HDL‐C levels, whereas the ε4 allele had an effect opposite to the el allele. These results indicate that the ε2 and ε4 alleles have the reciprocal effects on plasma lipid, lipoprotein and apo E levels.

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Crossref · 10.1111/j.1399-0004.1986.tb00547.x

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  • In humans and animal models, apoE genotype is correlated with apoE protein levels in plasma, with ε2 showing the highest protein levels and ε4 the lowest.

    “In humans and animal models, apoE genotype is correlated with apoE protein levels in plasma, with ␧2 showing the highest protein levels and ␧4 the lowest (Eto et al., 1986;Gregg et al., 1986;Raffai et al., 2001) (Fig. 2).”

    From Impact of Apolipoprotein E (ApoE) Polymorphism on Brain ApoE Levels (2008) · cites this paper as Eto et al., 1986

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Authors
Eto, M., Watanabe, K., & Ishii, K.
Affiliations
Asahikawa Medical University (JP)
Corresponding author
Eto, M.
Venue
Clinical Genetics
Publisher
Wiley
Published
1986-06
Volume
29
Issue
6
Pages
477-484
ISSN
  • 0009-9163 (ISSN-L)
  • 1399-0004
OpenAlex
W2149980542
Cited by
112
References
2
Citations by year
2026: 1 · 2024: 1 · 2022: 1 · 2021: 1 · 2019: 1 · 2017: 1 · 2016: 1 · 2015: 4 · 2014: 2 · 2013: 3 · 2012: 2
FWCI
9.72
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Genetics (publishedVersion)
  • PubMed (publishedVersion)
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 › Clinical Biochemistry › Paraoxonase enzyme and polymorphisms
Keywords
apolipoprotein E, plasma lipids, triglycerides, VLDL cholesterol, LDL cholesterol, HDL cholesterol, total cholesterol, normolipidemic subjects, Japanese population
MeSH terms
Adult, Alleles, Apolipoproteins E, Cholesterol, Female, Humans, Japan, Lipids, Cholesterol, HDL, Cholesterol, LDL, Lipoproteins, VLDL, Male, Middle Aged, Phenotype, Reference Values, Triglycerides, Cholesterol, VLDL, Apolipoprotein E4, Apolipoprotein E2

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