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Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia
BACKGROUND: Studies that have reported lower risk for cardiovascular outcomes in users of Sodium–Glucose Cotransporter-2 Inhibitors (SGLT-2i) are limited by residual cofounding and lack of information on prior cardiovascular disease (CVD). This study compared risk of cardiovascular events in patient...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472675/ https://www.ncbi.nlm.nih.gov/pubmed/37653496 http://dx.doi.org/10.1186/s12933-023-01963-9 |
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author | Vistisen, Dorte Carstensen, Bendix Elisabetta, Patorno Lanzinger, Stefanie Tan, Elise Chia-Hui Yabe, Daisuke Kim, Dae Jung Sheu, Wayne H.-H. Melzer-Cohen, Cheli Holl, Reinhard W. Núñez, Júlio Ha, Kyoung Hwa Halvorsen, Sigrun Langslet, Gisle Karasik, Avraham Nyström, Thomas Niskanen, Leo Guleria, Sonia Klement, Riho Carrasco, Marc Foersch, Johannes Shay, Christina Koeneman, Lisette Hoti, Fabian Farsani, Soulmaz Fazeli Khunti, Kamlesh Zaccardi, Francesco Subramanian, Anuradhaa Nirantharakumar, Krishnarajah |
author_facet | Vistisen, Dorte Carstensen, Bendix Elisabetta, Patorno Lanzinger, Stefanie Tan, Elise Chia-Hui Yabe, Daisuke Kim, Dae Jung Sheu, Wayne H.-H. Melzer-Cohen, Cheli Holl, Reinhard W. Núñez, Júlio Ha, Kyoung Hwa Halvorsen, Sigrun Langslet, Gisle Karasik, Avraham Nyström, Thomas Niskanen, Leo Guleria, Sonia Klement, Riho Carrasco, Marc Foersch, Johannes Shay, Christina Koeneman, Lisette Hoti, Fabian Farsani, Soulmaz Fazeli Khunti, Kamlesh Zaccardi, Francesco Subramanian, Anuradhaa Nirantharakumar, Krishnarajah |
author_sort | Vistisen, Dorte |
collection | PubMed |
description | BACKGROUND: Studies that have reported lower risk for cardiovascular outcomes in users of Sodium–Glucose Cotransporter-2 Inhibitors (SGLT-2i) are limited by residual cofounding and lack of information on prior cardiovascular disease (CVD). This study compared risk of cardiovascular events in patients within routine care settings in Europe and Asia with type 2 diabetes (T2D) initiating empagliflozin compared to dipeptidyl peptidase-4 inhibitors (DPP-4i) stratified by pre-existing CVD and history of heart failure (HF). METHODS AND RESULTS: Adults initiating empagliflozin and DPP-4i in 2014–2018/19 from 11 countries in Europe and Asia were compared using propensity score matching and Cox proportional hazards regression to assess differences in rates of primary outcomes: hospitalisation for heart failure (HHF), myocardial infarction (MI), stroke; and secondary outcomes: cardiovascular mortality (CVM), coronary revascularisation procedure, composite outcome including HHF or CVM, and 3-point major adverse cardiovascular events (MACE: MI, stroke and CVM). Country-specific results were meta-analysed and pooled hazard ratios (HR) with 95% confidence intervals (CI) from random-effects models are presented. In total, 85,244 empagliflozin/DPP4i PS-matched patient pairs were included with overall mean follow-up of 0.7 years. Among those with pre-existing CVD, lower risk was observed for HHF (HR 0.74; 95% CI 0.64–0.86), CVM (HR 0.55; 95% CI 0.38–0.80), HHF or CVM (HR 0.57; 95% CI 0.48–0.67) and stroke (HR 0.79; 95% CI 0.67–0.94) in patients initiating empagliflozin vs DPP-4i. Similar patterns were observed among patients without pre-existing CVD and those with and without pre-existing HF. CONCLUSION: These results from diverse patient populations in routine care settings across Europe and Asia demonstrate that initiation of empagliflozin compared to DPP-4i results in favourable cardioprotective effects regardless of pre-existing CVD or HF status. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-023-01963-9. |
format | Online Article Text |
id | pubmed-10472675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104726752023-09-02 Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia Vistisen, Dorte Carstensen, Bendix Elisabetta, Patorno Lanzinger, Stefanie Tan, Elise Chia-Hui Yabe, Daisuke Kim, Dae Jung Sheu, Wayne H.-H. Melzer-Cohen, Cheli Holl, Reinhard W. Núñez, Júlio Ha, Kyoung Hwa Halvorsen, Sigrun Langslet, Gisle Karasik, Avraham Nyström, Thomas Niskanen, Leo Guleria, Sonia Klement, Riho Carrasco, Marc Foersch, Johannes Shay, Christina Koeneman, Lisette Hoti, Fabian Farsani, Soulmaz Fazeli Khunti, Kamlesh Zaccardi, Francesco Subramanian, Anuradhaa Nirantharakumar, Krishnarajah Cardiovasc Diabetol Research BACKGROUND: Studies that have reported lower risk for cardiovascular outcomes in users of Sodium–Glucose Cotransporter-2 Inhibitors (SGLT-2i) are limited by residual cofounding and lack of information on prior cardiovascular disease (CVD). This study compared risk of cardiovascular events in patients within routine care settings in Europe and Asia with type 2 diabetes (T2D) initiating empagliflozin compared to dipeptidyl peptidase-4 inhibitors (DPP-4i) stratified by pre-existing CVD and history of heart failure (HF). METHODS AND RESULTS: Adults initiating empagliflozin and DPP-4i in 2014–2018/19 from 11 countries in Europe and Asia were compared using propensity score matching and Cox proportional hazards regression to assess differences in rates of primary outcomes: hospitalisation for heart failure (HHF), myocardial infarction (MI), stroke; and secondary outcomes: cardiovascular mortality (CVM), coronary revascularisation procedure, composite outcome including HHF or CVM, and 3-point major adverse cardiovascular events (MACE: MI, stroke and CVM). Country-specific results were meta-analysed and pooled hazard ratios (HR) with 95% confidence intervals (CI) from random-effects models are presented. In total, 85,244 empagliflozin/DPP4i PS-matched patient pairs were included with overall mean follow-up of 0.7 years. Among those with pre-existing CVD, lower risk was observed for HHF (HR 0.74; 95% CI 0.64–0.86), CVM (HR 0.55; 95% CI 0.38–0.80), HHF or CVM (HR 0.57; 95% CI 0.48–0.67) and stroke (HR 0.79; 95% CI 0.67–0.94) in patients initiating empagliflozin vs DPP-4i. Similar patterns were observed among patients without pre-existing CVD and those with and without pre-existing HF. CONCLUSION: These results from diverse patient populations in routine care settings across Europe and Asia demonstrate that initiation of empagliflozin compared to DPP-4i results in favourable cardioprotective effects regardless of pre-existing CVD or HF status. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-023-01963-9. BioMed Central 2023-08-31 /pmc/articles/PMC10472675/ /pubmed/37653496 http://dx.doi.org/10.1186/s12933-023-01963-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Vistisen, Dorte Carstensen, Bendix Elisabetta, Patorno Lanzinger, Stefanie Tan, Elise Chia-Hui Yabe, Daisuke Kim, Dae Jung Sheu, Wayne H.-H. Melzer-Cohen, Cheli Holl, Reinhard W. Núñez, Júlio Ha, Kyoung Hwa Halvorsen, Sigrun Langslet, Gisle Karasik, Avraham Nyström, Thomas Niskanen, Leo Guleria, Sonia Klement, Riho Carrasco, Marc Foersch, Johannes Shay, Christina Koeneman, Lisette Hoti, Fabian Farsani, Soulmaz Fazeli Khunti, Kamlesh Zaccardi, Francesco Subramanian, Anuradhaa Nirantharakumar, Krishnarajah Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title | Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title_full | Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title_fullStr | Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title_full_unstemmed | Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title_short | Empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: EMPagliflozin compaRative effectIveness and SafEty (EMPRISE) study results from Europe and Asia |
title_sort | empagliflozin is associated with lower cardiovascular risk compared with dipeptidyl peptidase-4 inhibitors in adults with and without cardiovascular disease: empagliflozin comparative effectiveness and safety (emprise) study results from europe and asia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472675/ https://www.ncbi.nlm.nih.gov/pubmed/37653496 http://dx.doi.org/10.1186/s12933-023-01963-9 |
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