Key result
Hypertension is linked to an over fourfold increase in MACE among people with HIV.
Why the study?
What are the incidence and risk factors for major adverse cardiovascular events in people living with HIV on long-term antiretroviral therapy?
Cohort (n=1,059)
What are the incidence and risk factors for major adverse cardiovascular events in people living with HIV on long-term antiretroviral therapy?
Hazard Ratio: 4.74
p-value: p=< 0.05
In people living with HIV on long-term ART, traditional cardiovascular risk factors, low baseline CD4+ count, and protease inhibitor use significantly increase the risk of MACE, highlighting the need for continuous cardiovascular monitoring and statin therapy when indicated.
People living with HIV (PLWH) continue to experience longer life expectancy due to effective antiretroviral therapy (ART). However, cardiovascular disease (CVD) has become a leading cause of morbidity and mortality. Despite improved HIV care, major adverse cardiovascular events (MACE) remain prevalent, with limited data from long-term cohorts. This study aimed to determine the incidence, risk factors, and predictors of MACE in long-term ACTHIV-IST cohort of PLWH in Istanbul. We conducted a retrospective analysis of 1059 patients followed for at least 10 years. Patients with prior MACE or noncardiac mortality were excluded. Traditional CVD risk factors, HIV-related immunovirological parameters, ART, and comorbidities were analyzed using Cox proportional hazards regression. MACE incidence was 7.55% (80/1059) with a cumulative rate of 11.1%. The most frequent events were ischemic heart disease (30.4%), myocardial infarction (27.6%), and sudden cardiac death (18.6%). Among those without traditional CVD risk factors, a CD4 + count <200 cells/mm 3 at diagnosis was associated with a 4.5-fold increased MACE risk. Hypertension (hazard ratio [HR]: 4.74), coronary artery disease (CAD) (HR: 8.49), and older age at HIV diagnosis (HR: 1.031/year) were the strongest independent predictors ( p < 0.05). Patients who should have used statins but did not were at higher risk of developing MACE (34% vs. 17%) compared to those who did ( p < 0.05). Twenty-one statin users of those who had MACE were before the event. A significantly higher MACE rate was observed in patients who used protease inhibitor (PI) compared to those who did not ( p = 0.002). Low baseline CD4 + T-cell count, prolonged HIV duration, comorbidities (e.g., hypertension, CAD, and dyslipidemia), PI experienced, and older age at HIV diagnosis significantly increase MACE risk. Early diagnosis, continuous cardiovascular monitoring, start statins if indicated, and individualized ART strategies are essential to reduce MACE-related morbidity and mortality in PLWH.
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Tahtasakal et al. (2025) conducted a cohort in HIV (n=1,059). Hypertension vs. No hypertension was evaluated on Major adverse cardiovascular events (MACE) (HR 4.74, p=< 0.05). In a 10-year cohort of 1059 people living with HIV, hypertension (HR 4.74) and coronary artery disease (HR 8.49) were strong independent predictors of major adverse cardiovascular events.
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