Efeito da empagliflozina para além do controlo glicémico

Bibliographic Details
Main Author: Monteiro, Pedro
Publication Date: 2019
Other Authors: Aguiar, Carlos, Matos, Pedro, Silva‐Nunes, José, Birne, Rita, Branco, Patrícia, Calado, Joaquim, Melo, Miguel, Polónia, Jorge
Format: Other
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10362/147518
Summary: The prevalence of type 2 diabetes (T2D) continues to increase, and its association with cardiovascular (CV) disease has led to the inclusion of CV endpoints in clinical trials on the treatment of T2D. This article explores the various trials already performed and under development in this field, with particular focus on the EMPA‐REG OUTCOME trial. In this trial, empagliflozin, a sodium‐glucose co‐transporter 2 inhibitor, demonstrated a reduction in CV risk in patients with T2D and established CV disease, in addition to CV safety and a decrease in glycated hemoglobin. This represents a paradigm shift that has led to changes in the international guidelines for the treatment of T2D. These results were maintained in subsequent subgroup analysis for heart failure, chronic kidney disease and peripheral arterial disease, although there are many questions concerning the mechanisms involved in these effects, including whether they are hemodynamic, metabolic or due to decreased myocardial cytoplasmic sodium concentrations. With this reduction in risk for major CV events in patients with T2D, the EMPA‐REG OUTCOME trial demonstrated CV protection from a hypoglycemic drug for the first time, and opened a new era in the treatment and management of T2D. This study has led to the development of ongoing trials that will establish which patients will benefit most from this therapy, particularly with regard to comorbidities.
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spelling Efeito da empagliflozina para além do controlo glicémicoEffect of empagliflozin beyond glycemic controlCardiovascular benefit in patients with type 2 diabetes and established cardiovascular diseasebenefício cardiovascular em doentes com DMT2 e doença cardiovascular estabelecidaCardiovascular diseaseDiabetesEmpagliflozinHeart failureCardiology and Cardiovascular MedicineSDG 3 - Good Health and Well-beingThe prevalence of type 2 diabetes (T2D) continues to increase, and its association with cardiovascular (CV) disease has led to the inclusion of CV endpoints in clinical trials on the treatment of T2D. This article explores the various trials already performed and under development in this field, with particular focus on the EMPA‐REG OUTCOME trial. In this trial, empagliflozin, a sodium‐glucose co‐transporter 2 inhibitor, demonstrated a reduction in CV risk in patients with T2D and established CV disease, in addition to CV safety and a decrease in glycated hemoglobin. This represents a paradigm shift that has led to changes in the international guidelines for the treatment of T2D. These results were maintained in subsequent subgroup analysis for heart failure, chronic kidney disease and peripheral arterial disease, although there are many questions concerning the mechanisms involved in these effects, including whether they are hemodynamic, metabolic or due to decreased myocardial cytoplasmic sodium concentrations. With this reduction in risk for major CV events in patients with T2D, the EMPA‐REG OUTCOME trial demonstrated CV protection from a hypoglycemic drug for the first time, and opened a new era in the treatment and management of T2D. This study has led to the development of ongoing trials that will establish which patients will benefit most from this therapy, particularly with regard to comorbidities.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)Centre for Toxicogenomics and Human Health (ToxOmics)RUNMonteiro, PedroAguiar, CarlosMatos, PedroSilva‐Nunes, JoséBirne, RitaBranco, PatríciaCalado, JoaquimMelo, MiguelPolónia, Jorge2023-01-13T22:11:31Z2019-102019-10-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/otherapplication/pdfhttp://hdl.handle.net/10362/147518por0870-2551PURE: 16260829https://doi.org/10.1016/j.repc.2019.02.008info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T18:08:07Zoai:run.unl.pt:10362/147518Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:38:35.611219Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Efeito da empagliflozina para além do controlo glicémico
Effect of empagliflozin beyond glycemic controlCardiovascular benefit in patients with type 2 diabetes and established cardiovascular disease
benefício cardiovascular em doentes com DMT2 e doença cardiovascular estabelecida
title Efeito da empagliflozina para além do controlo glicémico
spellingShingle Efeito da empagliflozina para além do controlo glicémico
Monteiro, Pedro
Cardiovascular disease
Diabetes
Empagliflozin
Heart failure
Cardiology and Cardiovascular Medicine
SDG 3 - Good Health and Well-being
title_short Efeito da empagliflozina para além do controlo glicémico
title_full Efeito da empagliflozina para além do controlo glicémico
title_fullStr Efeito da empagliflozina para além do controlo glicémico
title_full_unstemmed Efeito da empagliflozina para além do controlo glicémico
title_sort Efeito da empagliflozina para além do controlo glicémico
author Monteiro, Pedro
author_facet Monteiro, Pedro
Aguiar, Carlos
Matos, Pedro
Silva‐Nunes, José
Birne, Rita
Branco, Patrícia
Calado, Joaquim
Melo, Miguel
Polónia, Jorge
author_role author
author2 Aguiar, Carlos
Matos, Pedro
Silva‐Nunes, José
Birne, Rita
Branco, Patrícia
Calado, Joaquim
Melo, Miguel
Polónia, Jorge
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
Centre for Toxicogenomics and Human Health (ToxOmics)
RUN
dc.contributor.author.fl_str_mv Monteiro, Pedro
Aguiar, Carlos
Matos, Pedro
Silva‐Nunes, José
Birne, Rita
Branco, Patrícia
Calado, Joaquim
Melo, Miguel
Polónia, Jorge
dc.subject.por.fl_str_mv Cardiovascular disease
Diabetes
Empagliflozin
Heart failure
Cardiology and Cardiovascular Medicine
SDG 3 - Good Health and Well-being
topic Cardiovascular disease
Diabetes
Empagliflozin
Heart failure
Cardiology and Cardiovascular Medicine
SDG 3 - Good Health and Well-being
description The prevalence of type 2 diabetes (T2D) continues to increase, and its association with cardiovascular (CV) disease has led to the inclusion of CV endpoints in clinical trials on the treatment of T2D. This article explores the various trials already performed and under development in this field, with particular focus on the EMPA‐REG OUTCOME trial. In this trial, empagliflozin, a sodium‐glucose co‐transporter 2 inhibitor, demonstrated a reduction in CV risk in patients with T2D and established CV disease, in addition to CV safety and a decrease in glycated hemoglobin. This represents a paradigm shift that has led to changes in the international guidelines for the treatment of T2D. These results were maintained in subsequent subgroup analysis for heart failure, chronic kidney disease and peripheral arterial disease, although there are many questions concerning the mechanisms involved in these effects, including whether they are hemodynamic, metabolic or due to decreased myocardial cytoplasmic sodium concentrations. With this reduction in risk for major CV events in patients with T2D, the EMPA‐REG OUTCOME trial demonstrated CV protection from a hypoglycemic drug for the first time, and opened a new era in the treatment and management of T2D. This study has led to the development of ongoing trials that will establish which patients will benefit most from this therapy, particularly with regard to comorbidities.
publishDate 2019
dc.date.none.fl_str_mv 2019-10
2019-10-01T00:00:00Z
2023-01-13T22:11:31Z
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dc.relation.none.fl_str_mv 0870-2551
PURE: 16260829
https://doi.org/10.1016/j.repc.2019.02.008
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