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Dietary unsaturated fat increases HDL metabolic pathways involving apoE favorable to reverse cholesterol transport
Allyson M. Morton, … , Carlos O. Mendivil, Frank M. Sacks
Allyson M. Morton, … , Carlos O. Mendivil, Frank M. Sacks
Published April 4, 2019
Citation Information: JCI Insight. 2019;4(7):e124620. https://doi.org/10.1172/jci.insight.124620.
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Clinical Research and Public Health Metabolism

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

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Abstract

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.

Authors

Allyson M. Morton, Jeremy D. Furtado, Carlos O. Mendivil, Frank M. Sacks

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