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Cardiovascular risk evaluation and antiretroviral therapy effects in an HIV cohort: implications for clinical
Insights
This study reveals that modifiable factors like cholesterol and highly active antiretroviral therapy (HAART) duration significantly impact cardiovascular disease (CVD) risk in HIV patients. Regular risk assessments are crucial, especially during HAART.
Area of Science:
- Cardiology
- Infectious Diseases
- Public Health
Background:
- HIV infection is associated with an increased risk of cardiovascular disease (CVD).
- Highly active antiretroviral therapy (HAART) has transformed HIV management but may influence CVD risk.
- Understanding the CVD risk profile in HIV patients on HAART is crucial for preventative strategies.
Purpose of the Study:
- To determine the cardiovascular disease (CVD) risk profile of a large UK HIV cohort.
- To investigate the impact of highly active antiretroviral therapy (HAART) on CVD risk in this population.
Main Methods:
- A cross-sectional study involving 1021 HIV-positive outpatients.
- Demographics, HAART history, and CVD risk factors were recorded.
- Cardiovascular disease (CVD) and coronary heart disease (CHD) risks were calculated using the Framingham (1991) algorithm.
Main Results:
- Elevated cholesterol was a primary risk factor for CVD.
- Increased coronary heart disease (CHD) risk was strongly linked to the duration of HAART.
- CVD risk was higher in Caucasian patients compared to other ethnicities.
Conclusions:
- Modifiable risk factors, particularly cholesterol levels and HAART duration, are key determinants of CVD risk in HIV patients.
- Regular CVD and CHD risk assessment is recommended for all HIV patients, especially those on HAART.
- Consideration of HAART regimens' effects on CHD risk is vital during treatment selection.
Aims:
The aim of this study is to determine the cardiovascular disease (CVD) risk profile of a large UK HIV cohort and how highly active antiretroviral therapy (HAART) affects this.
Methods:
It is a cross-sectional study within a large inner city hospital and neighbouring district hospital. A total of 1021 HIV positive outpatients representative of the complete cohort and 990 who had no previous CVD were included in CVD risk analysis. We recorded demographics, HAART history and CVD risk factors. CVD and coronary heart disease (CHD) risks were calculated using the Framingham (1991) algorithm adjusted for family history.
Results:
The non-CVD cohort (n = 990) was 74% men, 51% Caucasian and 73.1% were on HAART. Mean age was 41 +/- 9 years, systolic blood pressure 120 +/- 14 mmHg, total cholesterol 4.70 +/- 1.05 mmol/l, high-density lipoprotein-C 1.32 +/- 0.48 mmol/l and 37% smoked. Median CVD risk was 4 (0-56) % in men and 1.4 (0-37) % in women; CHD risks were 3.5 (0-36) % and 0.6 (0-16) %. CVD risk was > 20% in 6% of men and 1% of women and > 10% in 12% of men and 4% of women. CVD risk was higher in Caucasians than other ethnicities; the risk factor contributing most was raised cholesterol. For patients on their first HAART, increased CHD risk (26.2% vs. 6.5%; odds ratio 4.03, p < 0.001) was strongly related to the duration of therapy.
Conclusions:
Modifiable risk factors, especially cholesterol, and also duration of HAART, were key determinants of CVD risk.
Discussion:
Regular CHD and/or CVD risk assessment should be performed on patients with HIV, especially during HAART therapy. The effect of different HAART regimens on CHD risk should be considered when selecting therapy.
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