Dietary unsaturated fat increases HDL metabolic pathways involving apoE favorable to reverse cholesterol transport.


Journal

JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073

Informations de publication

Date de publication:
04 04 2019
Historique:
received: 30 08 2018
accepted: 14 02 2019
entrez: 5 4 2019
pubmed: 5 4 2019
medline: 1 7 2020
Statut: epublish

Résumé

HDL that contains apolipoprotein E (apoE) is a subspecies especially active in steps in reverse cholesterol transport, a process that brings cholesterol from peripheral cells to the liver. Here, we studied the effect of dietary unsaturated fat compared with carbohydrate on the metabolism of HDL containing apoE. We enrolled 9 adults who were overweight or obese and had below-average HDL-cholesterol in a crossover study of a high-fat diet, primarily unsaturated, and a low-fat, high-carbohydrate diet. A metabolic tracer study was performed after each diet period. Dietary fat increased the secretion, metabolism, and clearance of HDL subspecies containing apoE. Dietary fat increased the rate of clearance of large cholesterol-rich HDL containing apoE and increased their conversion to small HDL containing apoE, indicating selective cholesterol ester delivery to the liver. The high-unsaturated-fat diet did not affect the metabolism of HDL lacking apoE. HDL containing apoE is a diet-responsive metabolic pathway that renders HDL more biologically active in reverse cholesterol transport. This may be a mechanism by which unsaturated fat protects against coronary heart disease. Protein-based HDL subspecies such as HDL containing apoE may be used to identify additional atheroprotective treatment targets not evident in the total HDL-cholesterol measurement. ClinicalTrials.gov NCT01399632. NIH and the National Center for Advancing Translational Science.

Sections du résumé

BACKGROUND
HDL that contains apolipoprotein E (apoE) is a subspecies especially active in steps in reverse cholesterol transport, a process that brings cholesterol from peripheral cells to the liver. Here, we studied the effect of dietary unsaturated fat compared with carbohydrate on the metabolism of HDL containing apoE.
METHODS
We enrolled 9 adults who were overweight or obese and had below-average HDL-cholesterol in a crossover study of a high-fat diet, primarily unsaturated, and a low-fat, high-carbohydrate diet. A metabolic tracer study was performed after each diet period.
RESULTS
Dietary fat increased the secretion, metabolism, and clearance of HDL subspecies containing apoE. Dietary fat increased the rate of clearance of large cholesterol-rich HDL containing apoE and increased their conversion to small HDL containing apoE, indicating selective cholesterol ester delivery to the liver. The high-unsaturated-fat diet did not affect the metabolism of HDL lacking apoE.
CONCLUSION
HDL containing apoE is a diet-responsive metabolic pathway that renders HDL more biologically active in reverse cholesterol transport. This may be a mechanism by which unsaturated fat protects against coronary heart disease. Protein-based HDL subspecies such as HDL containing apoE may be used to identify additional atheroprotective treatment targets not evident in the total HDL-cholesterol measurement.
TRIAL REGISTRATION
ClinicalTrials.gov NCT01399632.
FUNDING
NIH and the National Center for Advancing Translational Science.

Identifiants

pubmed: 30944249
pii: 124620
doi: 10.1172/jci.insight.124620
pmc: PMC6483656
doi:
pii:

Substances chimiques

Apolipoproteins E 0
Dietary Fats, Unsaturated 0
Lipoproteins, HDL 0
apolipoprotein E-rich HDL 0

Banques de données

ClinicalTrials.gov
['NCT01399632']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL095964
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007575
Pays : United States

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Auteurs

Allyson M Morton (AM)

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Jeremy D Furtado (JD)

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Carlos O Mendivil (CO)

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Frank M Sacks (FM)

Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Genetics and Complex Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

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Classifications MeSH