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Dulaglutide and cardiovascular and heart failure outcomes in patients with and without heart failure: a post-hoc analysis from the REWIND randomized trial
KRH. Branch, GR. Dagenais, A. Avezum, J. Basile, I. Conget, WC. Cushman, P. Jansky, M. Lakshmanan, F. Lanas, LA. Leiter, P. Pais, N. Pogosova, PJ. Raubenheimer, L. Ryden, JE. Shaw, WHH. Sheu, T. Temelkova-Kurktschiev, MA. Bethel, HC. Gerstein, R....
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu randomizované kontrolované studie, časopisecké články, práce podpořená grantem
NLK
Medline Complete (EBSCOhost)
od 2000-03-01 do Před 1 rokem
Wiley Free Content
od 1999 do Před 1 rokem
PubMed
36073143
DOI
10.1002/ejhf.2670
Knihovny.cz E-zdroje
- MeSH
- diabetes mellitus 2. typu * komplikace farmakoterapie epidemiologie MeSH
- hypoglykemika terapeutické užití škodlivé účinky MeSH
- inkretiny terapeutické užití MeSH
- kardiovaskulární nemoci * epidemiologie MeSH
- lidé MeSH
- srdeční selhání * farmakoterapie epidemiologie chemicky indukované MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
AIMS: People with diabetes are at high risk for cardiovascular events including heart failure (HF). We examined the effect of the glucagon-like peptide 1 agonist dulaglutide on incident HF events and other cardiovascular outcomes in those with or without prior HF in the randomized placebo-controlled Researching Cardiovascular Events with a Weekly Incretin in Diabetes (REWIND) trial. METHODS AND RESULTS: The REWIND major adverse cardiovascular event (MACE) outcome was the first occurrence of a composite endpoint of non-fatal myocardial infarction, non-fatal stroke, or death from cardiovascular causes (including unknown causes). In this post-hoc analysis, a HF event was defined as an adjudication-confirmed hospitalization or urgent evaluation for HF. Of the 9901 participants studied over a median follow-up of 5.4 years, 213/4949 (4.3%) randomly assigned to dulaglutide and 226/4952 (4.6%) participants assigned to placebo experienced a HF event (hazard ratio [HR] 0.93, 95% confidence interval [CI] 0.77-1.12; p = 0.456). In the 853 (8.6%) participants with HF at baseline, there was no change in either MACE or HF events with dulaglutide as compared to participants without HF (p = 0.44 and 0.19 for interaction, respectively). Combined cardiovascular death and HF events were marginally reduced with dulaglutide compared to placebo (HR 0.88, 95% CI 0.78-1.00; p = 0.050) but unchanged in patients with and without HF at baseline (p = 0.31). CONCLUSIONS: Dulaglutide was not associated with a reduction in HF events in patients with type 2 diabetes regardless of baseline HF status over 5.4 years of follow-up.
Baker Heart and Diabetes Institute Melbourne Victoria Australia
Department of Medicine K2 Karolinska Institute Stockholm Sweden
Division of Endocrinology and Metabolism Taipei Veterans General Hospital Taipei Taiwan
Division of Endocrinology University of Cape Town Cape Town South Africa
Eli Lilly and Co Indianapolis IN USA
Endocrinology and Nutrition Department Hospital Clínic i Universitari Barcelona Spain
International Research Center Hospital Alemão Oswaldo Cruz São Paulo Brazil
Li Ka Shing Knowledge Institute St Michael's Hospital University of Toronto Toronto Ontario Canada
Medical University of South Carolina Ralph H Johnson VA Medical Center Charleston SC USA
National Medical Research Center of Cardiology Moscow Russia
Robert Koch Medical Center Sofia Bulgaria
St John's Research Institute Bangalore India
Universidad de La Fontera Temuco Chile
University Hospital Motol Prague Czech Republic
University of Tennessee Health Science Center Memphis TN USA
Citace poskytuje Crossref.org
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