Cargando…

Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)

BACKGROUND: Reduction in cardiovascular death and hospitalization for heart failure (HHF) was recently reported with the sodium-glucose cotransporter-2 inhibitor (SGLT-2i) empagliflozin in patients with type 2 diabetes mellitus who have atherosclerotic cardiovascular disease. We compared HHF and dea...

Descripción completa

Detalles Bibliográficos
Autores principales: Kosiborod, Mikhail, Cavender, Matthew A., Fu, Alex Z., Wilding, John P., Khunti, Kamlesh, Holl, Reinhard W., Norhammar, Anna, Birkeland, Kåre I., Jørgensen, Marit Eika, Thuresson, Marcus, Arya, Niki, Bodegård, Johan, Hammar, Niklas, Fenici, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515629/
https://www.ncbi.nlm.nih.gov/pubmed/28522450
http://dx.doi.org/10.1161/CIRCULATIONAHA.117.029190
_version_ 1783251015651295232
author Kosiborod, Mikhail
Cavender, Matthew A.
Fu, Alex Z.
Wilding, John P.
Khunti, Kamlesh
Holl, Reinhard W.
Norhammar, Anna
Birkeland, Kåre I.
Jørgensen, Marit Eika
Thuresson, Marcus
Arya, Niki
Bodegård, Johan
Hammar, Niklas
Fenici, Peter
author_facet Kosiborod, Mikhail
Cavender, Matthew A.
Fu, Alex Z.
Wilding, John P.
Khunti, Kamlesh
Holl, Reinhard W.
Norhammar, Anna
Birkeland, Kåre I.
Jørgensen, Marit Eika
Thuresson, Marcus
Arya, Niki
Bodegård, Johan
Hammar, Niklas
Fenici, Peter
author_sort Kosiborod, Mikhail
collection PubMed
description BACKGROUND: Reduction in cardiovascular death and hospitalization for heart failure (HHF) was recently reported with the sodium-glucose cotransporter-2 inhibitor (SGLT-2i) empagliflozin in patients with type 2 diabetes mellitus who have atherosclerotic cardiovascular disease. We compared HHF and death in patients newly initiated on any SGLT-2i versus other glucose-lowering drugs in 6 countries to determine if these benefits are seen in real-world practice and across SGLT-2i class. METHODS: Data were collected via medical claims, primary care/hospital records, and national registries from the United States, Norway, Denmark, Sweden, Germany, and the United Kingdom. Propensity score for SGLT-2i initiation was used to match treatment groups. Hazard ratios for HHF, death, and their combination were estimated by country and pooled to determine weighted effect size. Death data were not available for Germany. RESULTS: After propensity matching, there were 309 056 patients newly initiated on either SGLT-2i or other glucose-lowering drugs (154 528 patients in each treatment group). Canagliflozin, dapagliflozin, and empagliflozin accounted for 53%, 42%, and 5% of the total exposure time in the SGLT-2i class, respectively. Baseline characteristics were balanced between the 2 groups. There were 961 HHF cases during 190 164 person-years follow-up (incidence rate, 0.51/100 person-years). Of 215 622 patients in the United States, Norway, Denmark, Sweden, and the United Kingdom, death occurred in 1334 (incidence rate, 0.87/100 person-years), and HHF or death in 1983 (incidence rate, 1.38/100 person-years). Use of SGLT-2i, versus other glucose-lowering drugs, was associated with lower rates of HHF (hazard ratio, 0.61; 95% confidence interval, 0.51–0.73; P<0.001); death (hazard ratio, 0.49; 95% confidence interval, 0.41–0.57; P<0.001); and HHF or death (hazard ratio, 0.54; 95% confidence interval, 0.48–0.60; P<0.001) with no significant heterogeneity by country. CONCLUSIONS: In this large multinational study, treatment with SGLT-2i versus other glucose-lowering drugs was associated with a lower risk of HHF and death, suggesting that the benefits seen with empagliflozin in a randomized trial may be a class effect applicable to a broad population of patients with type 2 diabetes mellitus in real-world practice. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT02993614.
format Online
Article
Text
id pubmed-5515629
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-55156292017-07-31 Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors) Kosiborod, Mikhail Cavender, Matthew A. Fu, Alex Z. Wilding, John P. Khunti, Kamlesh Holl, Reinhard W. Norhammar, Anna Birkeland, Kåre I. Jørgensen, Marit Eika Thuresson, Marcus Arya, Niki Bodegård, Johan Hammar, Niklas Fenici, Peter Circulation Original Research Articles BACKGROUND: Reduction in cardiovascular death and hospitalization for heart failure (HHF) was recently reported with the sodium-glucose cotransporter-2 inhibitor (SGLT-2i) empagliflozin in patients with type 2 diabetes mellitus who have atherosclerotic cardiovascular disease. We compared HHF and death in patients newly initiated on any SGLT-2i versus other glucose-lowering drugs in 6 countries to determine if these benefits are seen in real-world practice and across SGLT-2i class. METHODS: Data were collected via medical claims, primary care/hospital records, and national registries from the United States, Norway, Denmark, Sweden, Germany, and the United Kingdom. Propensity score for SGLT-2i initiation was used to match treatment groups. Hazard ratios for HHF, death, and their combination were estimated by country and pooled to determine weighted effect size. Death data were not available for Germany. RESULTS: After propensity matching, there were 309 056 patients newly initiated on either SGLT-2i or other glucose-lowering drugs (154 528 patients in each treatment group). Canagliflozin, dapagliflozin, and empagliflozin accounted for 53%, 42%, and 5% of the total exposure time in the SGLT-2i class, respectively. Baseline characteristics were balanced between the 2 groups. There were 961 HHF cases during 190 164 person-years follow-up (incidence rate, 0.51/100 person-years). Of 215 622 patients in the United States, Norway, Denmark, Sweden, and the United Kingdom, death occurred in 1334 (incidence rate, 0.87/100 person-years), and HHF or death in 1983 (incidence rate, 1.38/100 person-years). Use of SGLT-2i, versus other glucose-lowering drugs, was associated with lower rates of HHF (hazard ratio, 0.61; 95% confidence interval, 0.51–0.73; P<0.001); death (hazard ratio, 0.49; 95% confidence interval, 0.41–0.57; P<0.001); and HHF or death (hazard ratio, 0.54; 95% confidence interval, 0.48–0.60; P<0.001) with no significant heterogeneity by country. CONCLUSIONS: In this large multinational study, treatment with SGLT-2i versus other glucose-lowering drugs was associated with a lower risk of HHF and death, suggesting that the benefits seen with empagliflozin in a randomized trial may be a class effect applicable to a broad population of patients with type 2 diabetes mellitus in real-world practice. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT02993614. Lippincott Williams & Wilkins 2017-07-18 2017-05-18 /pmc/articles/PMC5515629/ /pubmed/28522450 http://dx.doi.org/10.1161/CIRCULATIONAHA.117.029190 Text en © 2017 The Authors. Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
spellingShingle Original Research Articles
Kosiborod, Mikhail
Cavender, Matthew A.
Fu, Alex Z.
Wilding, John P.
Khunti, Kamlesh
Holl, Reinhard W.
Norhammar, Anna
Birkeland, Kåre I.
Jørgensen, Marit Eika
Thuresson, Marcus
Arya, Niki
Bodegård, Johan
Hammar, Niklas
Fenici, Peter
Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title_full Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title_fullStr Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title_full_unstemmed Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title_short Lower Risk of Heart Failure and Death in Patients Initiated on Sodium-Glucose Cotransporter-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL Study (Comparative Effectiveness of Cardiovascular Outcomes in New Users of Sodium-Glucose Cotransporter-2 Inhibitors)
title_sort lower risk of heart failure and death in patients initiated on sodium-glucose cotransporter-2 inhibitors versus other glucose-lowering drugs: the cvd-real study (comparative effectiveness of cardiovascular outcomes in new users of sodium-glucose cotransporter-2 inhibitors)
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515629/
https://www.ncbi.nlm.nih.gov/pubmed/28522450
http://dx.doi.org/10.1161/CIRCULATIONAHA.117.029190
work_keys_str_mv AT kosiborodmikhail lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT cavendermatthewa lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT fualexz lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT wildingjohnp lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT khuntikamlesh lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT hollreinhardw lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT norhammaranna lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT birkelandkarei lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT jørgensenmariteika lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT thuressonmarcus lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT aryaniki lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT bodegardjohan lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT hammarniklas lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors
AT fenicipeter lowerriskofheartfailureanddeathinpatientsinitiatedonsodiumglucosecotransporter2inhibitorsversusotherglucoseloweringdrugsthecvdrealstudycomparativeeffectivenessofcardiovascularoutcomesinnewusersofsodiumglucosecotransporter2inhibitors