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Heart Failure, Investigator-Reported Sleep Apnea and Dapagliflozin: A Patient-Level Pooled Meta-Analysis of DAPA-HF and DELIVER.
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; Wilderäng, Ulrica; Solomon, Scott D; McMurray, John J V.
Affiliation
  • Butt JH; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK; Department of Cardiology, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
  • Jering K; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • DE Boer RA; Erasmus Medical Center, Rotterdam, The Netherlands.
  • Claggett BL; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Desai AS; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Hernandez AF; Duke University Medical Center, Durham, NC, USA.
  • Inzucchi SE; Yale School of Medicine, New Haven, CT, USA.
  • Jhund PS; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Køber L; Department of Cardiology, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
  • Kosiborod MN; Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City, Kansas City, MO, USA.
  • Lam CSP; National Heart Centre Singapore & Duke-National University of Singapore, Singapore.
  • Martinez FA; University of Cordoba, Cordoba, Argentina.
  • Ponikowski P; Center for Heart Diseases, University Hospital, Wroclaw Medical University, Wroclaw, Poland.
  • Sabatine MS; TIMI Study Group, Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Shah SJ; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Vaduganathan M; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Langkilde AM; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Bengtsson O; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Petersson M; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Sjöstrand M; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Wilderäng U; Late-Stage Development, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Solomon SD; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • McMurray JJV; British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK. Electronic address: john.mcmurray@glasgow.ac.uk.
J Card Fail ; 30(3): 436-448, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38104937
ABSTRACT

BACKGROUND:

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.

OBJECTIVES:

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).

METHODS:

A history of sleep apnea was investigator-reported. The primary outcome was a composite of worsening HF or cardiovascular death.

RESULTS:

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]) [Pinteraction = 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.

CONCLUSIONS:

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. CLINICAL TRIAL REGISTRATION Unique identifiers NCT01920711 CONDENSED ABSTRACT 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Benzhydryl Compounds / Heart Failure Type of study: Systematic_reviews Limits: Humans Language: En Journal: J Card Fail Journal subject: CARDIOLOGIA Year: 2024 Document type: Article Affiliation country: Denmark Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Benzhydryl Compounds / Heart Failure Type of study: Systematic_reviews Limits: Humans Language: En Journal: J Card Fail Journal subject: CARDIOLOGIA Year: 2024 Document type: Article Affiliation country: Denmark Country of publication: United States