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Subclinical cardiovascular disease in HIV controller and long-term nonprogressor populations
R M Brusca1, D B Hanna2, N I Wada3
1Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Insights
HIV controllers and long-term nonprogressors show similar cardiovascular disease risk as HIV-uninfected individuals, despite elevated inflammatory markers. Further research is needed to fully understand CVD risk in these populations.
Area of Science:
- Immunology and Virology
- Cardiovascular Disease Research
- HIV/AIDS Pathogenesis
Background:
- Individuals with Elite Control (ECs), Viremic Control (VCs), and Long-Term Nonprogression (LTNPs) manage HIV without antiretroviral therapy.
- Despite viral control, these HIV-infected groups may face an elevated risk of cardiovascular disease (CVD) compared to HIV-uninfected individuals.
- Understanding subclinical atherosclerosis and inflammation is crucial for assessing CVD risk in HIV controllers and LTNPs.
Purpose of the Study:
- To evaluate subclinical carotid and coronary atherosclerosis in HIV controllers, LTNPs, and HIV-uninfected individuals.
- To compare inflammatory biomarker levels across different HIV control categories and HIV-uninfected groups.
- To assess the association between HIV control status and the prevalence of atherosclerosis.
Main Methods:
- Carotid plaque presence and intima-media thickness (IMT) were measured in 1729 women and 1308 men.
- Coronary artery calcium and plaque were assessed in a subgroup of men.
- Serum inflammatory biomarkers (sCD163, sCD14, Gal-3, Gal-3BP, IL-6) were quantified and associated with HIV control categories.
Main Results:
- Carotid plaque prevalence and IMT were similar between HIV controllers, LTNPs, and HIV-uninfected individuals.
- HIV controllers and LTNPs exhibited lower carotid plaque prevalence than viremic HIV-infected individuals.
- Coronary atherosclerosis prevalence was comparable across HIV controllers/LTNPs, HIV-uninfected, and viremic HIV-infected men.
Conclusions:
- Subclinical cardiovascular disease (CVD) is similar in HIV controllers, LTNPs, and HIV-uninfected individuals, despite elevated inflammatory markers.
- Elevated levels of certain inflammatory biomarkers (sCD163, sCD14) were observed in controllers and LTNPs compared to HIV-uninfected persons.
- Further research is warranted to fully characterize CVD risk in HIV-infected individuals with elite control or long-term nonprogression.
Objectives:
Elite controllers (ECs), viraemic controllers (VCs), and long-term nonprogressors (LTNPs) control HIV viral replication or maintain CD4 T-cell counts without antiretroviral therapy, but may have increased cardiovascular disease (CVD) risk compared to HIV-uninfected persons. We evaluated subclinical carotid and coronary atherosclerosis and inflammatory biomarker levels among HIV controllers, LTNPs and noncontrollers and HIV-uninfected individuals in the Multicenter AIDS Cohort Study (MACS) and the Women's Interagency HIV Study (WIHS).
Methods:
We measured carotid plaque presence and common carotid artery intima-media thickness (IMT) in 1729 women and 1308 men, and the presence of coronary artery calcium and plaque in a subgroup of men. Associations between HIV control category and carotid and coronary plaque prevalences were assessed by multivariable regression analyses adjusting for demographics and CVD risk factors. Serum inflammatory biomarker concentrations [soluble CD163 (sCD163), soluble CD14 (sCD14), galectin-3 (Gal-3), galectin-3 binding protein (Gal-3BP) and interleukin (IL)-6] were measured and associations with HIV control category assessed.
Results:
We included 135 HIV controllers (30 ECs) and 135 LTNPs in the study. Carotid plaque prevalence and carotid IMT were similar in HIV controllers, LTNPs and HIV-uninfected individuals. HIV controllers and LTNPs had lower prevalences of carotid plaque compared to viraemic HIV-infected individuals. The prevalence of coronary atherosclerosis was similar in HIV controllers/LTNPs compared to HIV-uninfected and viraemic HIV-infected men. Controllers and LTNPs had higher concentrations of sCD163 and sCD14 compared to HIV-uninfected persons.
Conclusions:
Subclinical CVD was similar in HIV controllers, LTNPs and HIV-uninfected individuals despite elevated levels of some inflammatory biomarkers. Future studies of HIV controllers and LTNPs are needed to characterize the risk of CVD among HIV-infected persons.
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