Effect of Extended-Release Niacin on High-Density Lipoprotein (HDL) Functionality, Lipoprotein Metabolism, and Mediators of Vascular Inflammation in Statin-Treated Patients

J Am Heart Assoc. 2015 Sep 15;4(9):e001508. doi: 10.1161/JAHA.114.001508.

Abstract

Background: The aim of this study was to explore the influence of extended-release niacin/laropiprant (ERN/LRP) versus placebo on high-density lipoprotein (HDL) antioxidant function, cholesterol efflux, apolipoprotein B100 (apoB)-containing lipoproteins, and mediators of vascular inflammation associated with 15% increase in high-density lipoprotein cholesterol (HDL-C). Study patients had persistent dyslipidemia despite receiving high-dose statin treatment.

Methods and results: In a randomized double-blind, placebo-controlled, crossover trial, we compared the effect of ERN/LRP with placebo in 27 statin-treated dyslipidemic patients who had not achieved National Cholesterol Education Program-ATP III targets for low-density lipoprotein cholesterol (LDL-C). We measured fasting lipid profile, apolipoproteins, cholesteryl ester transfer protein (CETP) activity, paraoxonase 1 (PON1) activity, small dense LDL apoB (sdLDL-apoB), oxidized LDL (oxLDL), glycated apoB (glyc-apoB), lipoprotein phospholipase A2 (Lp-PLA2), lysophosphatidyl choline (lyso-PC), macrophage chemoattractant protein (MCP1), serum amyloid A (SAA) and myeloperoxidase (MPO). We also examined the capacity of HDL to protect LDL from in vitro oxidation and the percentage cholesterol efflux mediated by apoB depleted serum. ERN/LRP was associated with an 18% increase in HDL-C levels compared to placebo (1.55 versus 1.31 mmol/L, P<0.0001). There were significant reductions in total cholesterol, triglycerides, LDL cholesterol, total serum apoB, lipoprotein (a), CETP activity, oxLDL, Lp-PLA2, lyso-PC, MCP1, and SAA, but no significant changes in glyc-apoB or sdLDL-apoB concentration. There was a modest increase in cholesterol efflux function of HDL (19.5%, P=0.045), but no change in the antioxidant capacity of HDL in vitro or PON1 activity.

Conclusions: ERN/LRP reduces LDL-associated mediators of vascular inflammation, but has varied effects on HDL functionality and LDL quality, which may counter its HDL-C-raising effect.

Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01054508.

Keywords: HDL functionality; LDL quality; cholesterol efflux; extended‐release niacin; inflammation; laropiprant; oxidation.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Apolipoprotein B-100 / blood
  • Biomarkers / blood
  • Cholesterol, HDL / blood*
  • Cholesterol, LDL / blood*
  • Cross-Over Studies
  • Delayed-Action Preparations
  • Double-Blind Method
  • Drug Combinations
  • Dyslipidemias / blood
  • Dyslipidemias / diagnosis
  • Dyslipidemias / drug therapy*
  • England
  • Female
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Indoles / therapeutic use*
  • Inflammation Mediators / blood*
  • Lipoproteins, LDL / blood
  • Male
  • Middle Aged
  • Niacin / therapeutic use*
  • Time Factors
  • Treatment Outcome
  • Young Adult

Substances

  • APOB protein, human
  • Apolipoprotein B-100
  • Biomarkers
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Delayed-Action Preparations
  • Drug Combinations
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Indoles
  • Inflammation Mediators
  • Lipoproteins, LDL
  • MK-0524
  • oxidized low density lipoprotein
  • Niacin

Associated data

  • ClinicalTrials.gov/NCT01054508