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.