Literature DB >> 9409276

ApoE genotype does not predict lipid response to changes in dietary saturated fatty acids in a heterogeneous normolipidemic population. The DELTA Research Group. Dietary Effects on Lipoproteins and Thrombogenic Activity.

M Lefevre1, H N Ginsberg, P M Kris-Etherton, P J Elmer, P W Stewart, A Ershow, T A Pearson, P S Roheim, R Ramakrishnan, J Derr, D J Gordon, R Reed.   

Abstract

Recent studies have suggested that variations in apoE genotypes may influence the magnitude of plasma lipid changes in response to dietary interventions. We examined the ability of apoE genotype to predict plasma lipid response to reductions in percent of calories from total fat (TF) and saturated fat (SF) in a normolipidemic study population (n = 103) heterogeneous with respect to age, gender, race, and menopausal status. Three diets, an average American diet (34.3% TF, 15.0% SF), an AHA Step 1 diet (28.6% TF, 9.0% SF), and a low saturated fat (Low-Sat) diet (25.3% TF, 6.1% SF) were each fed for a period of 8 weeks in a three-way crossover design. Cholesterol was kept constant at 275 mg/d; monounsaturated and polyunsaturated fat were kept constant at approximately 13% and 6.5% of calories, respectively. Fasting lipid levels were measured during each of the final 4 weeks of each diet period. Participants were grouped by apoE genotype: E2 (E2/2, E2/3, E2/4); E3 (E3/3); E4 (E3/4, E4/4). Relative to the average American diet, both the Step 1 and Low-Sat diets significantly reduced total cholesterol, LDL cholesterol, and HDL cholesterol in all three apoE genotype groups. No evidence of a significant diet by genotype interaction, however, could be identified for any of the measured lipid and lipoprotein end points. Additional analysis of the data within individual population subgroup (men and women, blacks and whites) likewise provided no evidence of a significant diet by genotype interaction. Thus, in a heterogeneous, normolipidemic study population, apoE genotype does not predict the magnitude of lipid response to reductions in dietary saturated fat.

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Year:  1997        PMID: 9409276     DOI: 10.1161/01.atv.17.11.2914

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  5 in total

1.  Monthly haemostatic factor variability in women and men.

Authors:  Alison M Hill; Paul W Stewart; Mark K Fung; Penny M Kris-Etherton; Henry N Ginsberg; Russell P Tracy; Thomas A Pearson; Michael Lefevre; Roberta G Reed; Patricia J Elmer; Stephen Holleran; Abby G Ershow
Journal:  Eur J Clin Invest       Date:  2014       Impact factor: 4.686

2.  An association analysis between ApoA1 polymorphisms and the high-density lipoprotein (HDL) cholesterol level and myocardial infarction (MI) in Japanese.

Authors:  Keisuke Shioji; Toshifumi Mannami; Yoshihiro Kokubo; Yoichi Goto; Hiroshi Nonogi; Naoharu Iwai
Journal:  J Hum Genet       Date:  2004-07-17       Impact factor: 3.172

3.  A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population.

Authors:  Keisuke Shioji; Junko Nishioka; Hiroaki Naraba; Yoshihiro Kokubo; Toshifumi Mannami; Nozomu Inamoto; Kei Kamide; Shin Takiuchi; Masayoshi Yoshii; Yoshikazu Miwa; Yuhei Kawano; Toshiyuki Miyata; Shunichi Miyazaki; Yoichi Goto; Hiroshi Nonogi; Naomi Tago; Naoharu Iwai
Journal:  J Hum Genet       Date:  2004-02-21       Impact factor: 3.172

4.  Treatment of dyslipidemia: genetic interactions with diet and drug therapy.

Authors:  J M Ordovas; E J Schaefer
Journal:  Curr Atheroscler Rep       Date:  1999-07       Impact factor: 5.967

5.  Associations between apolipoprotein E genotype, diet, body mass index, and serum lipids in Lithuanian adult population.

Authors:  Janina Petkeviciene; Alina Smalinskiene; Dalia Ieva Luksiene; Kristina Jureniene; Vitalija Ramazauskiene; Jurate Klumbiene; Vaiva Lesauskaite
Journal:  PLoS One       Date:  2012-07-23       Impact factor: 3.240

  5 in total

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