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Measuring Frailty in HIV-infected Individuals. Identification of Frail Patients is the First Step to Amelioration and Reversal of Frailty
Published on: July 24, 2013
[Dyslipidemia and cardiovascular risk assessment in HIV-positive patients]
Serhat Uysal1, Mürşide Tuncel Başoğlu, Bahar Boydak
1Department of Infectious Diseases and Clinical Microbiology, Buca Seyfi Demirsoy State Hospital, Izmir, Turkey. drserhatuysal@gmail.com.
Insights
Antiretroviral treatment (ART) in HIV-positive patients significantly alters lipid profiles, increasing total cholesterol and LDL, while decreasing HDL. This elevates atherosclerotic cardiovascular disease (ASCVD) risk, necessitating close monitoring and intervention.
Area of Science:
- Cardiology
- Infectious Diseases
- Clinical Pharmacology
Background:
- Dyslipidemia is a significant complication associated with antiretroviral treatment (ART) for HIV.
- HIV infection itself can adversely affect lipid profiles and cardiovascular health.
Purpose of the Study:
- To screen baseline lipid levels and cardiovascular disease risk in HIV-positive patients.
- To analyze changes in lipid profiles and atherosclerotic cardiovascular disease (ASCVD) risk after ART initiation.
Main Methods:
- Retrospective review of HIV-positive patients' data, including lipid profiles (TC, TG, HDL, LDL), blood pressure, and lifestyle factors.
- Comparison of baseline lipid levels and ASCVD risk scores with data after ART initiation using American College of Cardiology guidelines.
Main Results:
- ART initiation was associated with significant increases in total cholesterol (TC) and low-density lipoprotein (LDL) levels (p<0.001).
- High-density lipoprotein (HDL) levels significantly decreased (p=0.001) post-ART.
- Atherosclerotic cardiovascular disease (ASCVD) risk scores significantly increased from baseline (46%) to the last visit (50%) (p<0.001).
Conclusions:
- HIV infection and its treatment with ART have detrimental effects on lipid profiles.
- Patients with HIV require close monitoring for dyslipidemia and elevated cardiovascular risk.
- Lifestyle interventions and lipid-lowering agents are crucial for managing cardiovascular risk in HIV-positive patients.
Objective:
Dyslipidemia is a major complication of antiretroviral treatment. Aim of the present study was to screen baseline lipid levels and cardiovascular disease risk in HIV-positive patients and analyze change in those parameters after initiation of antiretroviral treatment (ART).
Methods:
HIV-positive patients who presented at our clinic between April 2011 and August 2012 were included. Study included 19 female (22.1%) and 67 male (77.9%) patients (mean age 39.5±10.3 years). Blood pressure, smoking habit, alcohol consumption, serum total cholesterol (TC), triglyceride (TG), high-density lipoprotein (HDL), low-density lipoprotein (LDL), glucose level, and antiretroviral treatment status data were reviewed retrospectively. Changes in lipid profile and lifetime risk for atherosclerotic cardiovascular disease (ASCVD) according to the American College of Cardiology guidelines were compared with baseline data and analyzed.
Results:
At baseline, 13 (15.1%) patients were already receiving ART and 73 (84.9%) patients were treatment-naive or had stopped therapy ≥3 months prior to enrollment. At last visit, 73 (84.9%) patients were taking ART. Results of baseline and final visit TC levels were 175.5 mg/dL (range: 90-346 mg/dL) and 196.5 mg/dL (range: 104-317 mg/dL), respectively (p=0.001). HDL levels were 40 mg/dL (range: 21-81 mg/dL) and 35 mg/dL (range: 10-75 mg/dL; p=0.001), and LDL levels were 101.5 mg/dL (range: 32-191 mg/dL) and 120.5 mg/dL (range: 32-250 mg/dL; p<0.001). TG levels were 145.5 mg/dL (range: 43-2580 mg/dL and 152.5 mg/dL (range: 67-884 mg/dL; p=0.102). Baseline ASCVD risk score was 46% (range: 5-69%) while last visit ASCVD risk score was 50% (range: 5-69%; p<0.001).
Conclusion:
HIV infection has adverse effects on lipid profiles and cardiovascular risk of HIV-positive patients. Therefore, patients should be closely monitored for lifestyle interventions and lipid-lowering agents.
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