Literature DB >> 29322605

DECLARE-TIMI 58: Participants' baseline characteristics.

Itamar Raz1, Ofri Mosenzon1, Marc P Bonaca2, Avivit Cahn1, Eri T Kato3, Michael G Silverman2, Deepak L Bhatt2, Lawrence A Leiter4, Darren K McGuire5, John P H Wilding6, Ingrid A M Gause-Nilsson7, Anna M Langkilde7, Peter A Johansson7, Marc S Sabatine2, Stephen D Wiviott2.   

Abstract

AIM: To describe the baseline characteristics of participants randomized in the Dapagliflozin Effect on CardiovascuLAR Events (DECLARE-TIMI 58) trial, the pivotal study conducted to assess cardiovascular (CV) outcomes with dapagliflozin.
METHODS: The DECLARE-TIMI 58 trial will analyse 17 160 patients with type 2 diabetes randomized to treatment with dapagliflozin (10 mg/d) or matching placebo. We analysed their baseline characteristics.
RESULTS: The participants' mean ± SD age was 63.8 ± 6.8 years, 62.6% were male, and their mean ± SD diabetes duration was 11.8 ± 7.8 years, glycated haemoglobin 8.3% ± 1.2% (67 mmol/mol ± 9.7 mmol/mol) and body mass index 32.1 ± 6.0 kg/m2 . Randomization included 6971 (40.6%) patients with atherosclerotic CV disease (CVD), and 10 189 (59.4%) patients with multiple risk factors (MRF) for CVD (defined as men age ≥ 55 years or women ≥60 years, with at least one of dyslipidaemia, hypertension or smoking). Patients with CVD compared with patients with MRF were younger (62.5 ± 8.1 vs 64.7 ± 5.6 years), more frequently male (72.1% vs 56.1%), less often used metformin (74.6% vs 81.2%), more often used insulin (44.2% vs 36.4%), and more frequently used statins, aspirin, clopidogrel and β-blockers (82.2%, 71.1%, 24.7% and 66.6% vs 63.7%, 39.1%, 1.5% and 32.3%, respectively).
CONCLUSION: The DECLARE-TIMI 58 trial is expected to provide conclusive data on the effect of treatment with dapagliflozin in addition to standard of care, on CV outcomes in a broad patient population with type 2 diabetes and CVD or MRF for CVD.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  CVOTs; SGLT2 inhibitors; cardiovascular outcomes; dapagliflozin; type 2 diabetes

Mesh:

Substances:

Year:  2018        PMID: 29322605     DOI: 10.1111/dom.13217

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  34 in total

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