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Published on: November 10, 2017
The effects of extended release niacin on lipoprotein sub-particle concentrations in HIV-infected patients
Chunrong Lin1, Andrew Grandinetti, Cecilia Shikuma
1John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.
Insights
Extended Release Niacin (ERN) therapy improved lipid profiles in Human Immunodeficiency Virus (HIV) patients. ERN increased LDL size and decreased small LDL particles, showing safety and efficacy in this pilot study.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Cardiovascular Disease (CVD) is the leading cause of death in Human Immunodeficiency Virus (HIV) patients on highly active antiretroviral therapy (HAART).
- HIV patients often exhibit an atherogenic lipoprotein phenotype, characterized by small, low-density lipoprotein (SLDL) particles, elevated triglycerides, and low high-density lipoprotein cholesterol (HDL-C).
Purpose of the Study:
- To evaluate the efficacy of Extended Release Niacin (ERN) in improving lipid profiles in HIV-infected patients with low HDL-C levels.
Main Methods:
- A randomized controlled pilot study enrolled 17 HIV-positive subjects on HAART with HDL-C < 40 mg/dl.
- Nine subjects received ERN (titrated 500-1500 mg/night), and eight served as controls.
- Lipoprotein profiles were analyzed using Nuclear Magnetic Resonance (NMR) spectroscopy at baseline and 12 weeks.
Main Results:
- ERN treatment significantly increased overall LDL size (1.2% vs. -2.0% in controls, P=.04).
- ERN significantly decreased small LDL particle concentration (17.0% vs. 21.4% increase in controls, P=.03).
- One subject experienced flushing due to accidental overdose; otherwise, ERN was well-tolerated.
Conclusions:
- Extended Release Niacin (ERN) therapy is safe and effective for improving lipoprotein profiles in HIV-infected patients with low HDL-C.
- ERN may help mitigate the atherogenic lipoprotein phenotype associated with HIV and HAART.
Abstract:
With the advent of highly active antiretroviral therapy (HAART), Cardiovascular Disease (CVD) has emerged as the leading cause of death in Human Immunodeficiency Virus (HIV) infected patients. An atherogenic lipoprotein phenotype has been described in HIV- infected patients with a predominance of small, low density lipoprotein (SLDL) particles with accompanying elevated triglycerides and reduced high density lipoprotein cholesterol. This randomized controlled pilot study was conducted to evaluate the efficacy of Extended Release Niacin (ERN) in improving the lipid profile in HIV patients. A total of 17 HIV positive subjects on HAART therapy with High Density Lipoprotein Cholesterol (HDL) levels below 40mg/dl and Low Density Lipoprotein Cholesterol (LDL) below 130mg/dl were enrolled. Nine were randomized to be treated with ERN titrated from a starting level of 500mg/night and titrated to a level of 1500mg/night. Eight patients were assigned to the control arm. No placebo was used. Lipoprotein profiles of the subjects were analyzed at baseline and at the end of 12 weeks using Nuclear Magnetic Resonance (NMR) spectroscopy. At the end of 12 weeks, NMR spectroscopic analysis revealed a significant increase in overall LDL size (1.2% in ERN treated subjects vs 2.0% decrease in control patients, P=.04) and a decrease in small LDL particle concentration (17.0% in ERN treated subjects vs 21.4% increase in control patients, P=.03) in subjects receiving ERN as compared to those in the control group. Only 1 subject receiving ERN developed serious flushing which was attributed to an accidental overdose of the drug. This pilot study demonstrates that ERN therapy in HIV-infected patients with low HDL is safe and effective in improving the lipoprotein profile in these patients.
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