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Heart Failure, Investigator-Reported Sleep Apnea and Dapagliflozin: A Patient-Level Pooled Meta-Analysis of DAPA-HF and DELIVER.

Authors :
BUTT, JAWAD H.
JERING, KAROLA
DE BOER, RUDOLF A.
CLAGGETT, BRIAN L.
DESAI, AKSHAY S.
HERNANDEZ, ADRIAN F.
INZUCCHI, SILVIO E.
JHUND, PARDEEP S.
KØBER, LARS
KOSIBOROD, MIKHAIL N.
LAM, CAROLYN S.P.
MARTINEZ, FELIPE A.
PONIKOWSKI, PIOTR
SABATINE, MARC S.
SHAH, SANJIV J.
VADUGANATHAN, MUTHIAH
LANGKILDE, ANNA MARIA
BENGTSSON, OLOF
PETERSSON, MAGNUS
SJÖSTRAND, MIKAELA
Source :
Journal of Cardiac Failure; Mar2024, Vol. 30 Issue 3, p436-448, 13p
Publication Year :
2024

Abstract

• Whether dapagliflozin is beneficial in patients with sleep apnea and heart failure, across the range of ejection fractions, is unknown. • In a pooled individual-level meta-analysis of DAPA-HF and DELIVER, investigator-reported sleep apnea was associated with a greater risk of worsening heart failure events. • Dapagliflozin, compared with placebo, reduced the risk of clinical outcomes and improved health-related quality of life in patients with and without sleep apnea. Sleep apnea is more common in patients with heart failure (HF) than in the general population, but little is known about its association with clinical outcomes in various HF phenotypes or how it might modify the effect of HF therapy. To examine the prevalence of sleep apnea, its association with outcomes and the effects of dapagliflozin in patients with HF with and without sleep apnea in a pooled analysis of 2 trials comparing dapagliflozin to placebo in HFrEF (DAPA-HF trial) and HFmrEF/HFpEF (DELIVER trial). A history of sleep apnea was investigator-reported. The primary outcome was a composite of worsening HF or cardiovascular death. The prevalence of sleep apnea was 5.7% and 7.8% in patients with HFrEF and HFmrEF/HFpEF, respectively. The primary outcome occurred at a rate of 16.0 in participants with sleep apnea compared to 10.6 per 100 person-years in those without (adjusted HR 1.29 [95%CI, 1.10–1.52]). Compared with placebo, dapagliflozin reduced the risk of the primary endpoint to the same extent in patients with (HR 0.78 [95% CI, 0.59–1.03]) and without sleep apnea (HR 0.79 [0.72–0.87]) [P interaction = 0.93]. The beneficial effects of dapagliflozin on other clinical outcomes and symptom burden, physical function, and quality of life were consistent in participants with and without sleep apnea. In DAPA-HF and DELIVER, the true prevalence of sleep apnea was likely underestimated. An investigator-reported history of sleep apnea was associated with higher rates of worsening HF events. The benefits of dapagliflozin on clinical outcomes were consistent in patients with and without sleep apnea. Unique identifiers: NCT01920711 In a pooled analysis of the DAPA-HF and DELIVER trials of more than 11,000 patients with heart failure (HF) across the range of ejection fractions, an investigator-reported history of sleep apnea was associated with higher rates of worsening HF events but not mortality. The beneficial effects of dapagliflozin on clinical outcomes were consistent in patients with and without sleep apnea. These findings provide further evidence for dapagliflozin as a new treatment option for patients with heart failure across the range of ejection fractions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10719164
Volume :
30
Issue :
3
Database :
Supplemental Index
Journal :
Journal of Cardiac Failure
Publication Type :
Academic Journal
Accession number :
175833375
Full Text :
https://doi.org/10.1016/j.cardfail.2023.08.027