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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorZELNIKER, Thomas A.
dc.contributor.authorBONACA, Marc P.
dc.contributor.authorFURTADO, Remo H. M.
dc.contributor.authorMOSENZON, Ofri
dc.contributor.authorKUDER, Julia F.
dc.contributor.authorMURPHY, Sabina A.
dc.contributor.authorBHATT, Deepak L.
dc.contributor.authorLEITER, Lawrence A.
dc.contributor.authorMCGUIRE, Darren K.
dc.contributor.authorWILDING, John P. H.
dc.contributor.authorBUDAJ, Andrzej
dc.contributor.authorKISS, Robert G.
dc.contributor.authorPADILLA, Francisco
dc.contributor.authorGAUSE-NILSSON, Ingrid
dc.contributor.authorLANGKILDE, Anna Maria
dc.contributor.authorRAZ, Itamar
dc.contributor.authorSABATINE, Marc S.
dc.contributor.authorWIVIOTT, Stephen D.
dc.date.accessioned2020-06-01T15:01:33Z-
dc.date.available2020-06-01T15:01:33Z-
dc.date.issued2020
dc.identifier.citationCIRCULATION, v.141, n.15, p.1227-1234, 2020
dc.identifier.issn0009-7322
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/36229-
dc.description.abstractBackground: Atrial fibrillation (AF) and atrial flutter (AFL) are associated with both diabetes mellitus and its related comorbidities, including hypertension, obesity, and heart failure (HF). SGLT2 (sodium-glucose cotransporter 2) inhibitors have been shown to lower blood pressure, reduce weight, have salutary effects on left ventricular remodeling, and reduce hospitalization for HF and cardiovascular death in patients with type 2 diabetes mellitus. We therefore investigated whether SGLT2 inhibitors could also reduce the risk of AF/AFL. Methods: DECLARE-TIMI 58 (Dapagliflozin Effect on Cardiovascular Events-Thrombolysis in Myocardial Infarction 58) studied the efficacy and safety of the SGLT2 inhibitor dapagliflozin versus placebo in 17 160 patients with type 2 diabetes mellitus and either multiple risk factors for atherosclerotic cardiovascular disease (n=10 186) or known atherosclerotic cardiovascular disease (n=6974). We explored the effect of dapagliflozin on the first and total number of AF/AFL events in patients with (n=1116) and without prevalent AF/AFL using Cox and negative binomial models, respectively. AF/AFL events were identified by search of the safety database using MedDRA preferred terms (""atrial fibrillation,"" ""atrial flutter""). Results: Dapagliflozin reduced the risk of AF/AFL events by 19% (264 versus 325 events; 7.8 versus 9.6 events per 1000 patient-years; hazard ratio [HR], 0.81 [95% CI, 0.68-0.95]; P=0.009). The reduction in AF/AFL events was consistent regardless of presence or absence of a history of AF/AFL at baseline (previous AF/AFL: HR, 0.79 [95% CI, 0.58-1.09]; no AF/AFL: HR, 0.81 [95% CI, 0.67-0.98]; P for interaction 0.89). Similarly, presence of atherosclerotic cardiovascular disease (HR, 0.83 [95% CI, 0.66-1.04]) versus multiple risk factors (HR, 0.78 [95% CI, 0.62-0.99]; P for interaction 0.72) or a history of HF (HF: HR, 0.78 [95% CI, 0.55-1.11]; No HF: HR, 0.81 [95% CI, 0.68-0.97]; P for interaction 0.88) did not modify the reduction in AF/AFL events observed with dapagliflozin. Moreover, there was no effect modification by sex, history of ischemic stroke, glycated hemoglobin A(1c), body mass index, blood pressure, or estimated glomerular filtration rate (all P for interaction >0.20). Dapagliflozin also reduced the total number (first and recurrent) of AF/AFL events (337 versus 432; incidence rate ratio, 0.77 [95% CI, 0.64-0.92]; P=0.005). Conclusions: Dapagliflozin decreased the incidence of reported episodes of AF/AFL adverse events in high-risk patients with type 2 diabetes mellitus. This effect was consistent regardless of the patient's previous history of AF, atherosclerotic cardiovascular disease, or HF. Registration: URL: ; Unique identifier: NCT01730534.eng
dc.description.sponsorshipAstraZenecaAstraZeneca
dc.description.sponsorshipDeutsche ForschungsgemeinschaftGerman Research Foundation (DFG) [ZE 1109/1-1]
dc.description.sponsorshipLemann Foundation Cardiovascular Research Postdoctoral Fellowship -Harvard University/Brigham and Women's Hospital
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINSeng
dc.relation.ispartofCirculation
dc.rightsrestrictedAccesseng
dc.subjectatrial fibrillationeng
dc.subjectatrial fluttereng
dc.subjectdiabetes mellituseng
dc.subjectgliflozinseng
dc.subjectSGLT-2 inhibitorseng
dc.subject.othercotransporter 2 inhibitorseng
dc.subject.otherriskeng
dc.subject.otherpioglitazoneeng
dc.subject.othermetaanalysiseng
dc.subject.othermechanismeng
dc.subject.othereventseng
dc.titleEffect of Dapagliflozin on Atrial Fibrillation in Patients With Type 2 Diabetes Mellitus Insights From the DECLARE-TIMI 58 Trialeng
dc.typearticleeng
dc.rights.holderCopyright LIPPINCOTT WILLIAMS & WILKINSeng
dc.identifier.doi10.1161/CIRCULATIONAHA.119.044183
dc.identifier.pmid31983236
dc.subject.wosCardiac & Cardiovascular Systemseng
dc.subject.wosPeripheral Vascular Diseaseeng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalZELNIKER, Thomas A.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA; Vienna Gen Hosp, Div Cardiol, Vienna, Austria; Med Univ Vienna, Vienna, Austria
hcfmusp.author.externalBONACA, Marc P.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA; Univ Colorado, Sch Med, Dept Med, Div Cardiol, Aurora, CO USA; CPC Clin Res, Aurora, CO USA
hcfmusp.author.externalMOSENZON, Ofri:Hebrew Univ Jerusalem, Dept Endocrinol & Metab, Diabet Unit, Hadassah Med Ctr, Jerusalem, Israel
hcfmusp.author.externalKUDER, Julia F.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalMURPHY, Sabina A.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalBHATT, Deepak L.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalLEITER, Lawrence A.:Univ Toronto, Li Ka Shing Knowledge Inst, St Michaels Hosp, Toronto, ON, Canada
hcfmusp.author.externalMCGUIRE, Darren K.:Univ Texas Southwestern Med Ctr Dallas, Div Cardiol, Dallas, TX 75390 USA
hcfmusp.author.externalWILDING, John P. H.:Univ Liverpool, Inst Ageing & Chron Dis, Liverpool, Merseyside, England
hcfmusp.author.externalBUDAJ, Andrzej:Grochowski Hosp, Dept Cardiol, Ctr Postgrad Med Educ, Warsaw, Poland
hcfmusp.author.externalKISS, Robert G.:Mil Hosp, Dept Cardiol, Budapest, Hungary
hcfmusp.author.externalPADILLA, Francisco:Cardiol Clin & Intervencionista Tarascos, Guadalajara, Jalisco, Mexico
hcfmusp.author.externalGAUSE-NILSSON, Ingrid:AstraZeneca Gothenburg, Molndal, Sweden
hcfmusp.author.externalLANGKILDE, Anna Maria:AstraZeneca Gothenburg, Molndal, Sweden
hcfmusp.author.externalRAZ, Itamar:Hebrew Univ Jerusalem, Dept Endocrinol & Metab, Diabet Unit, Hadassah Med Ctr, Jerusalem, Israel
hcfmusp.author.externalSABATINE, Marc S.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.author.externalWIVIOTT, Stephen D.:Brigham & Womens Hosp, Cardiovasc Div, TIMI Study Grp, 75 Francis St, Boston, MA 02115 USA; Harvard Med Sch, Boston, MA 02115 USA
hcfmusp.description.beginpage1227
hcfmusp.description.endpage1234
hcfmusp.description.issue15
hcfmusp.description.volume141
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000528600200007
hcfmusp.origem.id2-s2.0-85083675930
hcfmusp.publisher.cityPHILADELPHIAeng
hcfmusp.publisher.countryUSAeng
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dc.description.indexMEDLINEeng
dc.identifier.eissn1524-4539
hcfmusp.citation.scopus230-
hcfmusp.scopus.lastupdate2024-03-29-
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