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Updated: Apr 4, 2026

Exergaming in Older People Living with HIV Improves Balance, Mobility and Ameliorates Some Aspects of Frailty
Published on: October 6, 2016
Telmisartan to reduce cardiovascular risk in older HIV-infected adults: a pilot study
Insights
Telmisartan did not significantly improve endothelial function in HIV-infected individuals. However, some subgroups like those on abacavir or protease inhibitors showed increased flow-mediated dilation (FMD), suggesting potential benefits.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Individuals with HIV face elevated cardiovascular disease (CVD) risk.
- Traditional CVD therapies require further study in this population.
- Telmisartan, an ARB and PPAR-gamma agonist, benefits endothelial function in HIV-uninfected populations.
Purpose of the Study:
- To assess telmisartan's effects on endothelial function in older HIV-infected individuals at risk for CVD.
- To evaluate changes in brachial artery flow-mediated dilation (FMD) as a measure of endothelial function.
Main Methods:
- A pilot study involving HIV-infected individuals aged 50+ on suppressive antiretroviral therapy (ART) with CVD risk factors.
- Open-label telmisartan 80 mg daily for 6 weeks.
- Brachial artery flow-mediated dilation (FMD) measured endothelial function, with the primary endpoint being the 6-week change in maximum relative FMD.
Main Results:
- 16 participants completed the study; 88% male, 65% non-White, median age 60.
- Significant reductions in systolic (-16.0 mmHg) and diastolic (-6.0 mmHg) blood pressure were observed.
- No significant overall change in FMD, but increased FMD noted in abacavir-treated, PI-treated, and non-smoking subsets.
Conclusions:
- Six weeks of telmisartan did not significantly alter endothelial function (FMD) in this cohort.
- Subgroup analyses suggest potential benefits in specific patient groups (abacavir/PI users, non-smokers).
- Further research is warranted to explore telmisartan's role in managing CVD risk factors in HIV-infected individuals.
Background:
HIV-infected persons are at increased cardiovascular disease (CVD) risk, but traditional CVD therapies are understudied in this population. Telmisartan is an angiotensin receptor blocker (ARB) and peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist that improves endothelial function and cardiovascular mortality in HIV-uninfected populations. We assessed the effects of telmisartan on endothelial function in older HIV-infected persons at risk for CVD in a small pilot study.
Methods:
HIV-infected individuals≥50 years old on suppressive antiretroviral therapy (ART) with ≥1 traditional CVD risk factor received open-label telmisartan 80 mg daily for 6 weeks. Brachial artery flow-mediated dilation (FMD) measured endothelial function. The primary endpoint was 6-week change in maximum relative FMD.
Results:
Seventeen participants enrolled; 16 completed all evaluations (88% men, 65% non-White, median age 60 years, CD4+T lymphocyte count 625 cells/mm3). Antiretroviral therapy included 71% protease inhibitor (PI), 29% non-nucleoside reverse transcriptase inhibitor (NNRTI), 29% integrase inhibitor, 65% tenofovir, and 29% abacavir. Cardiovascular disease risk factor prevalence included 76% hyperlipidemia, 65% hypertension, 18% smoking, and 12% diabetes mellitus. After 6 weeks, statistically significant blood pressure changes were observed (systolic-16.0 mmHg, diastolic-6.0 mmHg) without significant changes in FMD. In subset analyses, FMD increased more among abacavir-treated, PI-treated, and non-smoking participants.
Conclusions:
No significant FMD changes were observed after 6 weeks of telmisartan therapy; however, abacavir- and PI-treated participants and non-smokers showed greater FMD increases. Additional studies are needed to explore the effects of telmisartan on endothelial function among HIV-infected individuals with traditional CVD and/or ART-specific risk factors.
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