Key result
HIV infection is linked to ~52% higher risk of incident heart failure.
Cohort (n=120,765)
Yes
Answers are grounded in this paper and cite their sources.
BACKGROUND: Although the HIV can cause myocardial inflammation, the association of HIV infection with subsequent development of heart failure (HF) has not been extensively studied. This nationwide cohort study aimed to determine the risk of incident HF in people living with HIV/AIDS (PLWHA). METHODS: We identified PLWHA using the Taiwan Centers for Disease Control and Prevention HIV Surveillance System. An age- and sex-matched control group without HIV infection was selected from the Taiwan National Health Insurance Research Database for comparison. All patients were followed up until December 2014 and were observed for a new diagnosis of HF. A time-dependent Cox proportional hazards model was used to determine the association of HIV and highly active antiretroviral therapy with incident HF, with death as a competing risk event. RESULTS: Of the 120,765 patients (24,153 PLWHA and 96,612 matched controls), 641 (0.53%) had incident HF during a mean follow-up period of 5.84 years, including 192 (0.79%) PLWHA and 449 (0.46%) controls. Time to diagnosis of incident HF was significantly shorter in PLWHA than in those without HIV infection (P < 0.001, the log-rank test). After adjusting for age, sex, and comorbidities, HIV infection was found to be an independent risk factor for incident HF (adjusted hazard ratio, 1.52; 95% confidence interval: 1.27 to 1.82). As the duration of highly active antiretroviral therapy increased, the risk of HF decreased (P = 0.014). CONCLUSIONS: HIV infection was an independent risk factor for incident HF. Clinicians need to be aware of the higher risk of HF in PLWHA.
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Yen et al. (2018) conducted a cohort in HIV/AIDS and incident heart failure (n=120,765). HIV infection vs. Age- and sex-matched controls without HIV infection was evaluated on Incident heart failure (aHR 1.52, 95% CI 1.27-1.82, p=<0.001). HIV infection was independently associated with a higher risk of incident heart failure compared to matched uninfected controls (0.79% vs 0.46%; aHR 1.52; 95% CI 1.27-1.82).
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