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Published on: October 12, 2017
Lipid Metabolism and Cardiovascular Risk in HIV-1 Infection and HAART: Present and Future Problems
Sara Melzi1, Laura Carenzi, Maria Vittoria Cossu
11st Division of Infectious Diseases, "Luigi Sacco" Hospital, Via GB Grassi, 74, 20157 Milan, Italy.
Insights
Human immunodeficiency virus (HIV) infection and its treatments significantly impact lipid metabolism and cardiovascular risk. Further research is needed to balance HIV treatment effectiveness with cardiovascular health outcomes.
Area of Science:
- Infectious Diseases
- Cardiology
- Metabolic Disorders
Background:
- Infections, including human immunodeficiency virus (HIV), are linked to lipid metabolism disturbances and increased coronary heart disease (CHD) risk.
- HIV infection itself promotes hepatic lipogenesis and alters lipid profiles, with additional cardiovascular disease (CVD) risk amplified by lifestyle factors and comorbidities.
- Antiretroviral therapy (ART) can mitigate some risks but carries its own metabolic and cardiotoxic profiles.
Purpose of the Study:
- To highlight HIV-1's contribution to lipid alteration and inflammation.
- To examine the impact of antiretroviral therapy on cardiovascular risk in HIV-infected individuals.
- To discuss drug selection, statin/fibrate use, and switching strategies to minimize cardiovascular events.
Main Methods:
- Review of current literature and guidelines concerning HIV-1, lipid metabolism, and cardiovascular risk.
- Analysis of the effects of various antiretroviral drugs on lipid profiles and cardiotoxicity.
- Evaluation of treatment strategies, including early intervention and drug switching, to manage cardiovascular risk.
Main Results:
- HIV-1 significantly contributes to dyslipidemia and inflammation, increasing cardiovascular risk.
- Antiretroviral therapy, while essential, presents challenges due to drug-specific toxicities affecting lipid metabolism.
- The optimal timing for initiating HIV treatment to balance efficacy and cardiovascular safety remains unclear.
Conclusions:
- Early HIV treatment may reduce HIV's direct cardiovascular impact but could reveal drug-related adverse effects.
- The net effect of early treatment initiation on coronary heart disease and lipid abnormalities requires further investigation.
- Careful drug selection and management strategies are crucial for optimizing cardiovascular outcomes in the HIV-infected population.
Abstract:
Many infections favor or are directly implicated with lipid metabolism perturbations and/or increased risk of coronary heart disease (CHD). HIV itself has been shown to increase lipogenesis in the liver and to alter the lipid profile, while the presence of unsafe habits, addiction, comorbidities, and AIDS-related diseases increases substantially the risk of cardiovascular disease (CVD) in the HIV-infected population. Antiretroviral therapy reduces such stimuli but many drugs have intrinsic toxicity profiles impacting on metabolism or potential direct cardiotoxicity. In a moment when the main guidelines of HIV therapy are predating the point when to start treating, we mean to highlight the contribution of HIV-1 to lipid alteration and inflammation, the impact of antiretroviral therapy, the decisions on what drugs to use to reduce the probability of having a cardiovascular event, the increasing use of statins and fibrates in HIV-1 infected subjects, and finally the switch strategies, that balance effectiveness and toxicity to move the decision to change HIV drugs. Early treatment might reduce the negative effect of HIV on overall cardiovascular risk but may also evidence the impact of drugs, and the final balance (reduction or increase in CHD and lipid abnormalities) is not known up to date.
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