Literature DB >> 11120871

APO E gene and gene-environment effects on plasma lipoprotein-lipid levels.

J M Hagberg1, K R Wilund, R E Ferrell.   

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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Year:  2000        PMID: 11120871     DOI: 10.1152/physiolgenomics.2000.4.2.101

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  21 in total

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Journal:  Am J Hum Genet       Date:  2004-10-11       Impact factor: 11.025

2.  Do long-term HDL-C declines associated with a first birth vary by apo E phenotype? The Coronary Artery Risk Development in Young Adults (CARDIA) study.

Authors:  Erica P Gunderson; Rachel A Whitmer; Cora E Lewis; Charles P Quesenberry; Delia Smith West; Stephen Sidney
Journal:  J Womens Health (Larchmt)       Date:  2005-12       Impact factor: 2.681

3.  Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.

Authors:  R Durst; R Colombo; S Shpitzen; L B Avi; Y Friedlander; R Wexler; F J Raal; D A Marais; J C Defesche; M Y Mandelshtam; M J Kotze; E Leitersdorf; V Meiner
Journal:  Am J Hum Genet       Date:  2001-04-17       Impact factor: 11.025

4.  Serum vitamins A and E as modifiers of lipid trait genetics in the National Health and Nutrition Examination Surveys as part of the Population Architecture using Genomics and Epidemiology (PAGE) study.

Authors:  Logan Dumitrescu; Robert Goodloe; Kristin Brown-Gentry; Ping Mayo; Melissa Allen; Hailing Jin; Niloufar B Gillani; Nathalie Schnetz-Boutaud; Holli H Dilks; Dana C Crawford
Journal:  Hum Genet       Date:  2012-06-12       Impact factor: 4.132

5.  Apolipoprotein A5-1131T>C polymorphism, but not APOE genotypes, increases susceptibility for dyslipidemia in children and adolescents.

Authors:  D D V Brito; A P Fernandes; K B Gomes; F F Coelho; N G Cruz; A P Sabino; J E Cardoso; P P Figueiredo-Filho; R Diamante; C R Norton; M O Sousa
Journal:  Mol Biol Rep       Date:  2010-12-04       Impact factor: 2.316

6.  Apolipoprotein E4 is associated with improved cognitive function in Amazonian forager-horticulturalists with a high parasite burden.

Authors:  Benjamin C Trumble; Jonathan Stieglitz; Aaron D Blackwell; Hooman Allayee; Bret Beheim; Caleb E Finch; Michael Gurven; Hillard Kaplan
Journal:  FASEB J       Date:  2016-12-28       Impact factor: 5.191

7.  APOE modulates the correlation between triglycerides, cholesterol, and CHD through pleiotropy, and gene-by-gene interactions.

Authors:  Taylor J Maxwell; Christie M Ballantyne; James M Cheverud; Cameron S Guild; Chiadi E Ndumele; Eric Boerwinkle
Journal:  Genetics       Date:  2013-10-04       Impact factor: 4.562

8.  Selection on alleles affecting human longevity and late-life disease: the example of apolipoprotein E.

Authors:  Fotios Drenos; Thomas B L Kirkwood
Journal:  PLoS One       Date:  2010-04-02       Impact factor: 3.240

9.  Polymorphisms of the macrophage inflammatory protein 1 alpha and ApoE genes are associated with ulcerative colitis.

Authors:  Keshen Li; Binyou Wang; Hong Sui; Shengyuan Liu; Songpo Yao; Liang Guo; Dongwei Mao
Journal:  Int J Colorectal Dis       Date:  2008-09-02       Impact factor: 2.571

Review 10.  Apolipoprotein E4 as a target for developing new therapeutics for Alzheimer's disease.

Authors:  Lorenzo M Refolo; Howard M Fillit
Journal:  J Mol Neurosci       Date:  2004       Impact factor: 3.444

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