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Dulaglutide and incident atrial fibrillation or flutter in patients with type 2 diabetes: A post hoc analysis from the REWIND randomized trial
PJ. Raubenheimer, WC. Cushman, A. Avezum, J. Basile, I. Conget, G. Dagenais, A. Hoover, P. Jansky, F. Lanas, LA. Leiter, P. Lopez-Jaramillo, N. Pogosova, J. Probstfield, P. Rao-Melacini, L. Rydén, WH. Sheu, T. Temelkova-Kurktschiev, H. C Gerstein
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
PubMed
34984808
DOI
10.1111/dom.14634
Knihovny.cz E-zdroje
- MeSH
- diabetes mellitus 2. typu * komplikace farmakoterapie epidemiologie MeSH
- fibrilace síní * komplikace farmakoterapie epidemiologie MeSH
- glukagonu podobné peptidy analogy a deriváty MeSH
- hypoglykemika MeSH
- imunoglobuliny - Fc fragmenty škodlivé účinky MeSH
- lidé středního věku MeSH
- lidé MeSH
- rekombinantní fúzní proteiny škodlivé účinky MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
AIM: To assess the occurrence of atrial fibrillation or atrial flutter (atrial arrhythmias [AA]) in patients with type 2 diabetes treated with once-weekly subcutaneous dulaglutide versus placebo. MATERIALS AND METHODS: Patients without electrocardiographic (ECG)-confirmed AA at baseline and randomized in the REWIND trial were assessed for the development of AA based on an annual ECG. Additional analyses included whether dulaglutide compared with placebo reduced the composite outcome of AA or death, AA or cardiovascular death, AA or stroke and AA or heart failure. RESULTS: Among 9543 participants (mean age 66 ± 7 years, with cardiovascular risk factors and 31% with previous cardiovascular disease) without AA at entry in the trial, 524 patients (5.5%) had at least one episode of AA during the median 5.4 years of follow-up. Incident AA occurred in 269 of the 4769 participants allocated to dulaglutide (5.6%), at a rate of 10.7 per 1000 person-years, versus 255 of the 4774 allocated to placebo (5.3%), at a rate of 10.5 per 1000 person-years (P = .59). There was also no effect of dulaglutide on the composite outcome of AA and death or AA and heart failure. CONCLUSION: This post hoc analysis of data from the REWIND trial showed that treatment with dulaglutide was not associated with a reduced incidence of AA in this at-risk group of patients with type 2 diabetes.
Department of Medicine Karolinska Institut Stockholm Sweden
Department of Medicine University of Washington Seattle Washington USA
Division of Cardiology Medical University of South Carolina Charleston South Carolina USA
Division of Endocrinology Department of Medicine University of Cape Town Cape Town South Africa
Eli Lilly and Company Indianapolis Indiana USA
Endocrinology and Nutrition Department Hospital Clínic University of Barcelona 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
Masira Research Institute Medical School Universidad de Santander Bucaramanga Colombia
National Medical Research Center of Cardiology Moscow Russia
Robert Koch Medical Centre Sofia Bulgaria
Universidad de La Fontera Temuco Chile
University Hospital Motol Prague Czech Republic
University of Tennessee Health Science Center Memphis Tennessee USA
Citace poskytuje Crossref.org
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