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Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors
Published on: April 9, 2014
Cardiovascular effects of antiretroviral drugs: clinical review
Pasquale Perrone Filardi1, Stefania Paolillo, Caterina Marciano
1Department of Clinical Medicine, Cardiovascular and Immunological Sciences, Federico II University, Via Pansini, 5 80131 Naples, Italy. fpperron@unina.it
Insights
Highly active antiretroviral therapy (HAART) for HIV increases cardiovascular risk due to metabolic side effects. Managing these metabolic changes is crucial for improving outcomes in HIV patients.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Highly active antiretroviral therapy (HAART) for HIV is linked to increased cardiac events.
- Antiretroviral drugs cause metabolic side effects like dyslipidemia and abnormal fat distribution, raising cardiovascular risk in HIV patients.
- HIV infection, chronic inflammation, and traditional risk factors further elevate cardio- and cerebrovascular event incidence.
Purpose of the Study:
- To review the metabolic effects of antiretroviral drugs.
- To examine the contribution of combination antiretroviral therapy to cardiovascular risk in HIV patients.
Main Methods:
- Review of studies on metabolic side effects of antiretroviral therapy.
- Analysis of data linking protease inhibitor (PI) exposure to cardiovascular events.
- Examination of the DAD Study findings on myocardial infarction risk.
Main Results:
- Studies indicate carotid vascular impairment in patients on protease inhibitors (PI).
- The DAD Study showed a 26% increased risk of myocardial infarction with HAART, independently associated with PI exposure duration.
- Metabolic abnormalities associated with antiretroviral drugs contribute significantly to cardiovascular risk.
Conclusions:
- Assessing metabolic status before HAART initiation is vital.
- Controlling drug-related metabolic abnormalities can reduce cardiac events.
- Proactive management of metabolic effects improves prognosis for HIV patients.
Abstract:
In HIV infected patients an increased occurence of cardiac events has been demontrated from the introduction of highly active antiretroviral therapy (HAART). Antiretroviral drugs' regimens are, in fact, associated with several metabolic side effects, such as dyslipidemia, impaired glucose metabolism and abnormal body fat distribution, that increase the cardiovascular risk of HIV subjects. In addition, HIV infection itself, the chronic inflammatory status and the relevant presence in this population of some of the traditional cardiovascular risk factors contribute to an higher incidence of cardio and cerebrovascular events. In last years several studies showed the occurence of carotid vascular impairment in patients in treatment with protease inhibitors (PI). Similarly the DAD Study reported an increase of 26% of the risk of myocardial infarction in patients on HAART and that this risk is indipendently associated with longer exposure to PI, even after multivariate adjustments. A correct evaluation of the metabolic status before starting HAART and an adeguate control of the drugs-related metabolic abnormalities may reduce the incidence of cardiac events and still improve HIV patients prognosis. This review will focus on the metbolic effects of antiretroviral drugs and to the contribution of combination antiretroviral therapy on cardiovascular risk.
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