The Effect of High‐Dose Ascorbate Supplementation on Plasma Lipoprotein(a) Levels in Patients With Premature Coronary Heart Disease

Andrew G. Bostom, Anne L. Hume, Charles B. Eaton, Joseph P. Laurino, Lisa R. Yanek, Mary S. Regan, William H. McQuade, Wendy Y. Craig, Gayle Perrone, Paul F. Jacques

Research output: Contribution to journalArticle

Abstract

Study Objective. To determine the efficacy of high‐dose ascorbate supplementation in lowering lipoprotein(a) [Lp(a)] levels in patients with premature coronary heart disease (CHD). Design. Randomized, double‐blind, placebo‐controlled trial. Setting. Outpatient clinic. Patients. Forty‐four patients with documented premature CHD. defined as confirmed myocardial infarction and/or angiographically determined stenosis of 50% or greater in at least one major coronary artery before age 60 years. Interventions. Patients were block randomized on the basis of age, gender, and screening Lp(a) concentrations to receive ascorbate 4.5 g/day or placebo for 12 weeks. Measurements and Main Results. High‐dose ascorbate was well tolerated and produced a marked elevation in mean plasma ascorbate levels (+1.2 mg/dl; p<0.001). Multiple linear regression analysis revealed no significant effect of supplementation on postintervention Lp(a) levels (p=0.39) in a model that included treatment group assignment, and baseline Lp(a) levels. Conclusions. Our findings do not support a clinically important lowering effect of high‐dose ascorbate on plasma Lp(a) in patients with premature CHD. 1995 Pharmacotherapy Publications Inc.

Original languageEnglish (US)
Pages (from-to)458-464
Number of pages7
JournalPharmacotherapy: The Journal of Human Pharmacology and Drug Therapy
Volume15
Issue number4
DOIs
StatePublished - Jan 1 1995

ASJC Scopus subject areas

  • Pharmacology (medical)

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