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Heart Failure among People with HIV: Evolving Risks, Mechanisms, and Preventive Considerations
Mabel Toribio1, Tomas G Neilan2, Markella V Zanni3
1Metabolism Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, 55 Fruit Street, 5 LON 207, Boston, MA, 02114, USA.
People with HIV (PHIV) on antiretroviral therapy (ART) have double the risk of heart failure. Understanding mechanisms like diastolic dysfunction is key to developing new preventive strategies for heart conditions in PHIV.
Area of Science:
- Cardiology
- Infectious Diseases
- Public Health
Background:
- People with HIV (PHIV) on modern antiretroviral therapy (ART) face a doubled risk of heart failure compared to HIV-uninfected individuals.
- While advanced HIV/AIDS can cause reduced cardiac function, ART-treated HIV is linked to heart failure with reduced ejection fraction (HFrEF) or preserved ejection fraction (HFpEF).
Purpose of the Study:
- To review the evolving risks, mechanisms, and preventive strategies for heart failure in people with HIV.
- To address the increased incidence of heart failure, particularly HFpEF, in ART-treated PHIV.
Main Methods:
- Literature review of studies on HIV, ART, and cardiovascular outcomes.
- Analysis of mechanisms contributing to heart failure in PHIV, including diastolic dysfunction, myocardial fibrosis, and myocardial steatosis.
- Discussion of current challenges and future directions in cardiovascular risk management for PHIV.
Main Results:
- ART-treated HIV is associated with both HFrEF and HFpEF.
- Diastolic dysfunction, characterized by a "stiff" left ventricle, is a key feature of HFpEF in PHIV.
- Hypertension, immune activation, and metabolic dysregulation are common in ART-treated PHIV and contribute to myocardial fibrosis and steatosis, driving diastolic dysfunction.
- HFpEF is challenging to treat with conventional therapies and carries high morbidity and mortality.
- Diastolic dysfunction, myocardial fibrosis, and myocardial steatosis are potentially reversible.
Conclusions:
- Achieving UNAIDS 90-90-90 goals can reduce AIDS-related mortality, including cardiovascular deaths.
- Further research into the mechanisms predisposing ART-treated PHIV to heart failure, especially HFpEF, is crucial.
- Developing targeted preventive strategies is essential for preserving myocardial health in PHIV.
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