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Extended-Release Niacin Alters the Metabolism of Plasma Apolipoprotein (Apo) A-I and ApoB-Containing Lipoproteins

  • Stefania Lamon-Fava
  • , Margaret R Diffenderfer
  • , P Hugh R Barrett
  • , Aaron Buchsbaum
  • , Mawuli Nyaku
  • , Katalin V Horvath
  • , Bela F Asztalos
  • , Seiko Otokozawa
  • , Masumi Ai
  • , Nirupa R Matthan
  • , Alice H Lichtenstein
  • , Gregory G Dolnikowski
  • , Ernst J Schaefer

Research output: Contribution to journalArticlepeer-review

148 Citations (Scopus)

Abstract

Objectives— Extended-release niacin effectively lowers plasma TG levels and raises plasma high-density lipoprotein (HDL) cholesterol levels, but the mechanisms responsible for these effects are unclear. Methods and Results— We examined the effects of extended-release niacin (2 g/d) and extended-release niacin (2 g/d) plus lovastatin (40 mg/d), relative to placebo, on the kinetics of apolipoprotein (apo) A-I and apoA-II in HDL, apoB-100 in TG-rich lipoproteins (TRL), intermediate-density lipoproteins (IDL) and low-density lipoproteins (LDL), and apoB-48 in TRL in 5 men with combined hyperlipidemia. Niacin significantly increased HDL cholesterol and apoA-I concentrations, associated with a significant increase in apoA-I production rate (PR) and no change in fractional catabolic rate (FCR). Plasma TRL apoB-100 levels were significantly lowered by niacin, accompanied by a trend toward an increase in FCR and no change in PR. Niacin treatment significantly increased TRL apoB-48 FCR but had no effect on apoB-48 PR. No effects of niacin on concentrations or kinetic parameters of IDL and LDL apoB-100 and HDL apoA-II were noted. The addition of lovastatin to niacin promoted a lowering in LDL apoB-100 attributable to increased LDL apoB-100 FCR. Conclusion— Niacin treatment was associated with significant increases in HDL apoA-I concentrations and production, as well as enhanced clearance of TRL apoB-100 and apoB-48.
Original languageEnglish
Pages (from-to)1672-1678
JournalArteriosclerosis, Thrombosis, and Vascular Biology
Volume28
Issue number9
DOIs
Publication statusPublished - 19 Jun 2008

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