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SGLT2 inhibitor therapy and clinical outcomes in HIV-related cardiomyopathy
Hesham Sheashaa1, Ramzi Ibrahim1, Hoang Nhat Pham2,3
1Department of Cardiovascular Medicine, Mayo Clinic, Phoenix, AZ, USA.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) significantly reduce mortality and hospitalizations in patients with HIV cardiomyopathy (HIV-CM). This finding offers new hope for managing this complex cardiovascular condition.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- HIV cardiomyopathy (HIV-CM) presents significant health risks.
- Sodium-glucose cotransporter 2 inhibitors (SGLT2i) show promise for heart failure (HF).
- The efficacy of SGLT2i in HIV-CM remains largely unexplored.
Purpose of the Study:
- To investigate the impact of SGLT2i on outcomes in patients with HIV-CM.
- To compare mortality and hospitalization rates between HIV-CM patients with and without SGLT2i therapy.
Main Methods:
- A cohort of 2606 patients with HIV-CM was analyzed using the TriNetX Network.
- Patients receiving SGLT2i were propensity score matched with a control group not on SGLT2i.
- Primary endpoint was all-cause mortality; secondary endpoints included hospitalizations and major adverse cardiovascular events.
Main Results:
- SGLT2i use was linked to a significant reduction in all-cause mortality (HR 0.475).
- SGLT2i therapy also significantly decreased all-cause hospitalizations (HR 0.725).
- No significant differences were found for acute heart failure, myocardial infarction, stroke, or cardiac arrest.
Conclusions:
- SGLT2i therapy demonstrates a significant survival benefit for patients with HIV-CM.
- SGLT2i use is associated with reduced hospitalization rates in this patient population.
- Further research may elucidate SGLT2i's role in specific cardiovascular event prevention within HIV-CM.
Background:
HIV cardiomyopathy (HIV-CM) is associated with significant morbidity and mortality. Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have benefits in heart failure (HF), but their role in the specialized population of HIV-CM is poorly understood.
Methods:
Patients in the TriNetX Network with HIV-CM and SGLT2i therapy were compared to a propensity matched control group of patients with HIV-CM without SGLT2i use. The primary endpoint was all-cause mortality, secondary endpoints included all-cause hospitalizations, acute HF, stroke, acute myocardial infarction (MI), cardiac arrest, atrial fibrillation and ventricular tachycardia.
Results:
In the total of 2606 included patients, SGLT2i therapy was associated with significant reduction in all-cause mortality (HR 0.475, 95%CI 0.337-0.671), all-cause hospitalization (HR 0.725, 95%CI 0.646-0.814). No significant differences were observed in the individual outcomes of acute HF, MI, stroke, or cardiac arrest.
Conclusion:
SGLT2i use was associated with significant reductions in all-cause mortality and hospitalizations in patients with HIV-CM.
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