Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/26570
Title: Extended-Release Niacin Alters the Metabolism of Plasma Apolipoprotein (Apo) A-I and ApoB-Containing Lipoproteins
Contributor(s): Lamon-Fava, Stefania (author); Diffenderfer, Margaret R (author); Barrett, P Hugh R  (author)orcid ; Buchsbaum, Aaron (author); Nyaku, Mawuli (author); Horvath, Katalin V (author); Asztalos, Bela F (author); Otokozawa, SeikoAi, MasumiMatthan, Nirupa RLichtenstein, Alice HDolnikowski, Gregory GSchaefer, Ernst J
Publication Date: 2008-06-19
Open Access: Yes
DOI: 10.1161/ATVBAHA.108.164541Open Access Link
Handle Link: https://hdl.handle.net/1959.11/26570
Open Access Link: https://www.doi.org/10.1161/ATVBAHA.108.164541Open Access Link
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.
Publication Type: Journal Article
Grant Details: NHMRC/58-1950-4-401
Source of Publication: Arteriosclerosis, Thrombosis, and Vascular Biology, 28(9), p. 1672-1678
Publisher: Lippincott Williams & Wilkins
Place of Publication: United States of America
ISSN: 1079-5642
1524-4636
Fields of Research (FoR) 2008: 110399 Clinical Sciences not elsewhere classified
Socio-Economic Objective (SEO) 2008: 920103 Cardiovascular System and Diseases
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Appears in Collections:Journal Article

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