Patient Characteristics, Clinical Outcomes, and Effect of Dapagliflozin in Relation to Duration of Heart Failure: Is It Ever Too Late to Start a New Therapy?


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 10 11 2020
medline: 18 3 2021
entrez: 9 11 2020
Statut: ppublish

Résumé

The impact of heart failure (HF) duration on outcomes and treatment effect is largely unknown. We aim to compare baseline patient characteristics, outcomes, and the efficacy and safety of dapagliflozin, in relation to time from diagnosis of HF in DAPA-HF trial (Dapagliflozin and Prevention of Adverse-outcomes in Heart Failure). HF duration was categorized as ≥2 to ≤12 months, >1 to 2 years, >2 to 5 years, and >5 years. Outcomes were adjusted for prognostic variables and analyzed using Cox regression. The primary end point was the composite of worsening HF or cardiovascular death. Treatment effect was examined within each duration category and by duration threshold. The number of patients in each category was: 1098 (≥2-≤12 months), 686 (>1-2 years), 1105 (>2-5 years), and 1855 (>5 years). Longer-duration HF patients were older and more comorbid with worse symptoms. The rate of the primary outcome (per 100 person-years) increased with HF duration: 10.2 (95% CI, 8.7-12.0) for ≥2 to ≤12 months, 10.6 (8.7-12.9) >1 to 2 years, 15.5 (13.6-17.7) >2 to 5 years, and 15.9 (14.5-17.6) for >5 years. Similar trends were seen for all other outcomes. The benefit of dapagliflozin was consistent across HF duration and on threshold analysis. The hazard ratio for the primary outcome ≥2 to ≤12 months was 0.86 (0.63-1.18), >1 to 2 years 0.95 (0.64-1.42), >2 to 5 years 0.74 (0.57-0.96), and >5 years 0.64 (0.53-0.78), Longer-duration HF patients were older, had more comorbidity and symptoms, and higher rates of worsening HF and death. The benefits of dapagliflozin were consistent across HF duration. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03036124.

Sections du résumé

BACKGROUND
The impact of heart failure (HF) duration on outcomes and treatment effect is largely unknown. We aim to compare baseline patient characteristics, outcomes, and the efficacy and safety of dapagliflozin, in relation to time from diagnosis of HF in DAPA-HF trial (Dapagliflozin and Prevention of Adverse-outcomes in Heart Failure).
METHODS
HF duration was categorized as ≥2 to ≤12 months, >1 to 2 years, >2 to 5 years, and >5 years. Outcomes were adjusted for prognostic variables and analyzed using Cox regression. The primary end point was the composite of worsening HF or cardiovascular death. Treatment effect was examined within each duration category and by duration threshold.
RESULTS
The number of patients in each category was: 1098 (≥2-≤12 months), 686 (>1-2 years), 1105 (>2-5 years), and 1855 (>5 years). Longer-duration HF patients were older and more comorbid with worse symptoms. The rate of the primary outcome (per 100 person-years) increased with HF duration: 10.2 (95% CI, 8.7-12.0) for ≥2 to ≤12 months, 10.6 (8.7-12.9) >1 to 2 years, 15.5 (13.6-17.7) >2 to 5 years, and 15.9 (14.5-17.6) for >5 years. Similar trends were seen for all other outcomes. The benefit of dapagliflozin was consistent across HF duration and on threshold analysis. The hazard ratio for the primary outcome ≥2 to ≤12 months was 0.86 (0.63-1.18), >1 to 2 years 0.95 (0.64-1.42), >2 to 5 years 0.74 (0.57-0.96), and >5 years 0.64 (0.53-0.78),
CONCLUSIONS
Longer-duration HF patients were older, had more comorbidity and symptoms, and higher rates of worsening HF and death. The benefits of dapagliflozin were consistent across HF duration. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03036124.

Identifiants

pubmed: 33164553
doi: 10.1161/CIRCHEARTFAILURE.120.007879
pmc: PMC7610491
mid: EMS119217
doi:

Substances chimiques

Benzhydryl Compounds 0
Biomarkers 0
Glucosides 0
Sodium-Glucose Transporter 2 Inhibitors 0
dapagliflozin 1ULL0QJ8UC

Banques de données

ClinicalTrials.gov
['NCT03036124']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007879

Subventions

Organisme : British Heart Foundation
ID : RE/18/6/34217
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Références

JACC Heart Fail. 2014 Oct;2(5):440-6
pubmed: 25194291
Am J Cardiol. 2019 Aug 15;124(4):554-559
pubmed: 31221464
Acta Cardiol. 2020 Apr 7;:1-11
pubmed: 32252602
Stat Med. 1985 Jan-Mar;4(1):87-90
pubmed: 3992076
Eur J Heart Fail. 2020 Oct;22(10):1786-1789
pubmed: 32374051
Circulation. 2020 Jan 14;141(2):90-99
pubmed: 31736335
ESC Heart Fail. 2020 Oct 19;:
pubmed: 33078584
Eur J Heart Fail. 2019 May;21(5):665-675
pubmed: 30895697
J Am Coll Cardiol. 2017 Jun 27;69(25):3029-3039
pubmed: 28641792
Eur J Heart Fail. 2019 Nov;21(11):1402-1411
pubmed: 31309699
Eur Heart J. 2016 Nov 01;37(41):3167-3174
pubmed: 27354044
N Engl J Med. 2019 Nov 21;381(21):1995-2008
pubmed: 31535829
Eur J Heart Fail. 2020 Oct;22(10):1777-1785
pubmed: 32227556
Eur J Heart Fail. 2018 Feb;20(2):373-381
pubmed: 29027329

Auteurs

Su E Yeoh (SE)

BHF Cardiovascular Research Centre, University of Glasgow, United Kingdom (S.E.Y., P.D., P.S.J., J.J.V.M.).

Pooja Dewan (P)

BHF Cardiovascular Research Centre, University of Glasgow, United Kingdom (S.E.Y., P.D., P.S.J., J.J.V.M.).

Pardeep S Jhund (PS)

BHF Cardiovascular Research Centre, University of Glasgow, United Kingdom (S.E.Y., P.D., P.S.J., J.J.V.M.).

Silvio E Inzucchi (SE)

Section of Endocrinology, Yale University School of Medicine, New Haven, CT (S.E.I.).

Lars Køber (L)

Department of Cardiology, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark (L.K.).

Mikhail N Kosiborod (MN)

Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City (M.N.K.).

Felipe A Martinez (FA)

National University of Cordoba, Argentina (F.A.M.).

Piotr Ponikowski (P)

Wroclaw Medical University, Poland (P.P.).

Marc S Sabatine (MS)

The TIMI Study Group (M.S.S.), Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Scott D Solomon (SD)

Cardiovascular Division (S.D.S.), Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Olof Bengtsson (O)

AstraZeneca, Gothenburg, Sweden (O.B., M.S., A.M.L.).

Mikaela Sjöstrand (M)

AstraZeneca, Gothenburg, Sweden (O.B., M.S., A.M.L.).

Anna Maria Langkilde (AM)

AstraZeneca, Gothenburg, Sweden (O.B., M.S., A.M.L.).

John J V McMurray (JJV)

BHF Cardiovascular Research Centre, University of Glasgow, United Kingdom (S.E.Y., P.D., P.S.J., J.J.V.M.).

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH