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De-Intensification of Antidiabetic Treatment Using Canagliflozin in Patients with Heart Failure and Type 2 Diabetes: Cana-Switch-HF Study

dc.contributor.authorPérez-Belmonte, Luis M.
dc.contributor.authorRicci, Michele
dc.contributor.authorSanz-Cánovas, Jaime
dc.contributor.authorCobos-Palacios, Lidia
dc.contributor.authorLópez-Carmona, María D.
dc.contributor.authorRuiz-Moreno, M. Isabel
dc.contributor.authorMillán-Gómez, Mercedes
dc.contributor.authorBernal-López, M. Rosa
dc.contributor.authorJansen-Chaparro, Sergio
dc.contributor.authorGómez-Huelgas, Ricardo
dc.contributor.authoraffiliation[Pérez-Belmonte,LM; Ricci,M; Sanz-Cánovas,J; Cobos-Palacios,L; López-Carmona,MD; Ruiz-Moreno,MI; Bernal-López,MR; Jansen-Chaparro,S; Gómez-Huelgas,R] Servicio de Medicina Interna, Hospital Regional Universitario de Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga (UMA), Málaga, Spain. [Pérez-Belmonte,LM] Servicio de Medicina Interna, Hospital Helicópteros Sanitarios, Marbella, Spain. [Pérez-Belmonte,LM; Millán-Gómez,M] Centro de Investigación Biomédica en Red Enfermedades Cardiovasculares (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain. [Bernal-López,MR; Gómez-Huelgas,R] Centro de Investigación Biomédica en Red Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Madrid, Spain.
dc.contributor.funderThis work was supported by PI15/00256 from the Institute of Health “Carlos III” (ISCIII), co-funded by the Fondo Europeo de Desarrollo Regional-FEDER. Maria Isabel Queipo-Ortuño was supported by the “Miguel Servet Type II” program (CPI18/00003, ISCIII, Spain, co-funded by the Fondo Europeo de Desarrollo Regional-FEDER) and by the “Nicolas Monardes” research program of the Consejería de Salud (C-0030-2018, Junta de Andalucía, Spain. Bruno Ramos Molina was supported by the “Miguel Servet Type I” program (CP19/00098, ISCIII, Spain, co-funded by the Fondo Europeo de Desarrollo Regional-FEDER). Lidia Sanchez-Alcoholado was the recipient of a predoctoral grant (PE-0106-2019) from the Consejería de Salud y Familia (co-funded by the Fondo Europeo de Desarrollo Regional-FEDER, Andalucia, Spain). Aurora Laborda-Illanes was the recipient of a predoctoral grant, PFIS-ISCIII (FI19-00112), co-funded by the Fondo Europeo de Desarrollo Regional-FEDER, Madrid, Spain.
dc.date.accessioned2022-12-20T11:36:39Z
dc.date.available2022-12-20T11:36:39Z
dc.date.issued2021-05-08
dc.description.abstractCanagliflozin is a sodium-glucose co-transporter 2 inhibitor that reduces glycemia as well as the risk of cardiovascular events. Our main objective was to analyze antidiabetic treatment de-intensification and the glycemic efficacy of replacing antidiabetic agents (excluding metformin) with canagliflozin in patients with heart failure and type 2 diabetes with poor glycemic control. In this observational, retrospective, real-world study, we selected patients treated with metformin in combination with ≥2 non-insulin antidiabetic agents or metformin in combination with basal insulin plus ≥1 non-insulin antidiabetic agent. Non-insulin antidiabetic agents were replaced with canagliflozin. Patients were followed-up on at three, six, and 12 months after the switch and a wide range of clinical variables were recorded. A total of 121 patients were included. From baseline to 12 months, the number of antidiabetic agents (3.1 ± 1.0 vs. 2.1 ± 0.8, p < 0.05), basal insulin dose (20.1 ± 9.8 vs. 10.1 ± 6.5 units, p < 0.01), and percentage of patients who used basal insulin (47.9% vs. 31.3%, p < 0.01) decreased. The proportion of patients who used diuretics also declined significantly. In addition, we observed improvement in glycemic control, with an increase in the proportion of patients with glycated hemoglobin <7% from 16.8% at three months to 63.5% at 12 (p < 0.001). Canagliflozin use was also beneficial in terms of body weight, blood pressure, heart failure status, functional class, and cardiovascular-renal risk. There were also reductions in the number of emergency department visits and hospitalizations for heart failure. Moreover, canagliflozin was well-tolerated, with a low rate of drug-related discontinuation. Mounting evidence from randomized controlled trials and real-world studies point to the beneficial profile of sodium-glucose co-transporter type 2 inhibitors such as canagliflozin in patients with heart failure.es_ES
dc.description.versionYeses_ES
dc.identifier.citationPérez-Belmonte LM, Ricci M, Sanz-Cánovas J, Cobos-Palacios L, López-Carmona MD, Ruiz-Moreno MI, et al. De-Intensification of Antidiabetic Treatment Using Canagliflozin in Patients with Heart Failure and Type 2 Diabetes: Cana-Switch-HF Study. J Clin Med. 2021 May 8;10(9):2013es_ES
dc.identifier.doi10.3390/jcm10092013es_ES
dc.identifier.essn2077-0383
dc.identifier.pmcPMC8125841
dc.identifier.pmid34066707es_ES
dc.identifier.urihttp://hdl.handle.net/10668/4533
dc.journal.titleJournal of Clinical Medicine
dc.language.isoen
dc.page.number11 p.
dc.provenanceRealizada la curación de contenido 21/02/2025
dc.publisherMDPIes_ES
dc.relation.publisherversionhttps://www.mdpi.com/2077-0383/10/9/2013es_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectDe-intensificationes_ES
dc.subjectEfficacyes_ES
dc.subjectCanagliflozines_ES
dc.subjectHeart failurees_ES
dc.subjectType 2 diabeteses_ES
dc.subjectCapacidad de respuestaes_ES
dc.subjectEficaciaes_ES
dc.subjectCanagliflozinaes_ES
dc.subjectInsuficiencia cardíacaes_ES
dc.subjectDiabetes mellitus tipo 2es_ES
dc.subjectHipoglucemianteses_ES
dc.subject.meshMedical Subject Headings::Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Physiological Effects of Drugs::Hypoglycemic Agentses_ES
dc.subject.meshMedical Subject Headings::Chemicals and Drugs::Organic Chemicals::Amidines::Guanidines::Biguanides::Metformines_ES
dc.subject.meshMedical Subject Headings::Diseases::Endocrine System Diseases::Diabetes Mellitus::Diabetes Mellitus, Type 2es_ES
dc.subject.meshMedical Subject Headings::Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Peptide Hormones::Pancreatic Hormones::Insulinses_ES
dc.subject.meshMedical Subject Headings::Diseases::Nutritional and Metabolic Diseases::Metabolic Diseases::Glucose Metabolism Disorders::Hyperglycemiaes_ES
dc.subject.meshMedical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Therapeutics::Patient Care::Hospitalizationes_ES
dc.subject.meshMedical Subject Headings::Chemicals and Drugs::Inorganic Chemicals::Metals::Metals, Alkali::Sodiumes_ES
dc.subject.meshMedical Subject Headings::Chemicals and Drugs::Carbohydrates::Monosaccharides::Hexoses::Glucosees_ES
dc.subject.meshMedical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies::Retrospective Studieses_ES
dc.subject.meshMedical Subject Headings::Diseases::Cardiovascular Diseases::Heart Diseases::Heart Failurees_ES
dc.subject.meshMedical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Therapeuticses_ES
dc.titleDe-Intensification of Antidiabetic Treatment Using Canagliflozin in Patients with Heart Failure and Type 2 Diabetes: Cana-Switch-HF Studyes_ES
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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