Related Experiment Video
Updated: Aug 10, 2026

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017
Coronary heart disease risk, dyslipidemia, and management in HIV-infected persons
1Division of Infectious Diseases, Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0405, USA. Carl.Fichtenbaum@uc.edu
Insights
Highly active antiretroviral therapy (HAART) improves longevity in human immunodeficiency virus (HIV) patients but can cause dyslipidemia and coronary heart disease (CHD). Managing these risks involves careful antiretroviral (ARV) selection and lipid-lowering strategies.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Highly active antiretroviral therapy (HAART) has increased survival for individuals with human immunodeficiency virus (HIV).
- All classes of HAART drugs are linked to atherogenic lipid profile changes, increasing coronary heart disease (CHD) risk.
- Managing dyslipidemia and CHD in HIV patients often follows non-HIV guidelines, but drug interactions complicate treatment.
Purpose of the Study:
- To review the impact of HAART on lipid profiles and CHD risk in HIV-infected individuals.
- To discuss current and evolving strategies for managing dyslipidemia in the context of HIV treatment.
- To highlight the importance of ARV selection and lipid-lowering therapies in preventing cardiovascular complications.
Main Methods:
- Review of current literature on HAART, dyslipidemia, and CHD in HIV-infected populations.
- Analysis of the effects of different antiretroviral (ARV) drug classes on lipid profiles.
- Discussion of management strategies, including lifestyle modifications, ARV switching, and lipid-lowering agents.
Main Results:
- All HAART drug classes can induce atherogenic lipid changes.
- Lipid-lowering drugs may interact with ARVs, complicating management.
- Emerging data on ARV-specific lipid effects are influencing clinical practice.
Conclusions:
- Aggressively treat atherogenic dyslipidemia in HIV patients.
- Prioritize ARVs with lower CHD potential or switch to them.
- Consider lipid-lowering therapy when ARV modification is insufficient or not feasible.
Abstract:
Dyslipidemia and coronary heart disease (CHD) are of increasing concern in persons with human immunodeficiency virus (HIV) infection who are living longer because of the benefits of highly active antiretroviral therapy (HAART). All classes of drugs used in HAART have been associated with atherogenic changes in lipid profiles. The management of HIV-infected persons with dyslipidemia and/or CHD currently emphasizes the importance of monitoring and optimizing lipid levels through lifestyle changes, switching antiretrovirals (ARVs), and lipid-lowering treatments utilizing guidelines developed for persons without HIV infection. In HIV-infected persons, the use of lipid-lowering drugs may result in pharmacokinetic interactions with ARVs, complicating the management of patients. Recent advances in our understanding of the differential effects of specific ARVs on lipids is beginning to alter the clinical approach to management. In the absence of randomized clinical trials, clinicians should aggressively treat atherogenic dyslipidemia by primarily utilizing or switching to ARVs with the lowest potential to induce CHD or, when this is not possible or is ineffective, secondarily by the addition of lipid-lowering therapy. The current optimal management of HIV infection requires careful selection of ARVs with consideration given to the potential development of CHD and an understanding of how to manage dyslipidemia.
Related Concept Videos
Retrovirus Life Cycles
Lipid-Lowering Drugs: Statins and Miscellaneous Agents
Coronary Artery Disease I: Introduction
Coronary Artery Disease IV: Preventive Measures
Angina IV: Management
Atherosclerosis III: Management

