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Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes

BACKGROUND: Sodium-glucose cotransporter 2 (SGLT2) inhibition reduces cardiovascular events in type 2 diabetes (T2DM) and is associated with a reduction in left ventricular (LV) mass index. However, the impact on right ventricular (RV) remodeling is unknown. Accordingly, the objective of this study...

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Autores principales: Sarak, Bradley, Verma, Subodh, David Mazer, C., Teoh, Hwee, Quan, Adrian, Gilbert, Richard E., Goodman, Shaun G., Bami, Karan, Coelho-Filho, Otávio R., Ahooja, Vineeta, Deva, Djeven P., Garg, Vinay, Gandhi, Sumeet, Connelly, Kim A., Yan, Andrew T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491405/
https://www.ncbi.nlm.nih.gov/pubmed/34607574
http://dx.doi.org/10.1186/s12933-021-01390-8
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author Sarak, Bradley
Verma, Subodh
David Mazer, C.
Teoh, Hwee
Quan, Adrian
Gilbert, Richard E.
Goodman, Shaun G.
Bami, Karan
Coelho-Filho, Otávio R.
Ahooja, Vineeta
Deva, Djeven P.
Garg, Vinay
Gandhi, Sumeet
Connelly, Kim A.
Yan, Andrew T.
author_facet Sarak, Bradley
Verma, Subodh
David Mazer, C.
Teoh, Hwee
Quan, Adrian
Gilbert, Richard E.
Goodman, Shaun G.
Bami, Karan
Coelho-Filho, Otávio R.
Ahooja, Vineeta
Deva, Djeven P.
Garg, Vinay
Gandhi, Sumeet
Connelly, Kim A.
Yan, Andrew T.
author_sort Sarak, Bradley
collection PubMed
description BACKGROUND: Sodium-glucose cotransporter 2 (SGLT2) inhibition reduces cardiovascular events in type 2 diabetes (T2DM) and is associated with a reduction in left ventricular (LV) mass index. However, the impact on right ventricular (RV) remodeling is unknown. Accordingly, the objective of this study was to assess the impact of SGLT2 inhibition on RV parameters and function in T2DM and coronary artery disease (CAD). METHODS: In EMPA-HEART CardioLink-6, 97 patients with T2DM and CAD were randomly assigned to empagliflozin 10 mg (n = 49) once daily or placebo (n = 48). Cardiac magnetic resonance imaging was performed at baseline and after 6 months. RV mass index (RVMi), RV end-diastolic and end-systolic volume index (RVEDVi, RVESVi) and RV ejection fraction (RVEF) were assessed in blinded fashion. RESULTS: At baseline, mean RVMi (± SD) (11.8 ± 2.4 g/m(2)), RVEF (53.5 ± 4.8%), RVEDVi (64.3 ± 13.2 mL/m(2)) and RVESVi (29.9 ± 6.9 mL/m(2)) were within normal limits and were similar between the empagliflozin and placebo groups. Over 6 months, there were no significant differences in RVMi (− 0.11 g/m(2), [95% CI − 0.81 to 0.60], p = 0.76), RVEF (0.54%, [95% CI − 1.4 to 2.4], p = 0.58), RVEDVi (− 1.2 mL/m(2), [95% CI − 4.1 to 1.7], p = 0.41) and RVESVi (− 0.81 mL/m(2), [95% CI − 2.5 to 0.90], p = 0.35) in the empaglifozin group as compared with the placebo group. In both groups, there was no significant correlation between RVMi and LVMi changes from baseline to 6 months. CONCLUSIONS: In this post-hoc analysis, SGLT2 inhibition with empagliflozin had no impact on RVMi and RV volumes in patients with T2DM and CAD. The potentially differential effect of empagliflozin on the LV and RV warrants further investigation. Clinical Trial Registration: URL: https://www.clinicaltrials.gov/ct2/show/NCT02998970?cond=NCT02998970&draw=2&rank=1. Unique identifier: NCT02998970.
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spelling pubmed-84914052021-10-05 Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes Sarak, Bradley Verma, Subodh David Mazer, C. Teoh, Hwee Quan, Adrian Gilbert, Richard E. Goodman, Shaun G. Bami, Karan Coelho-Filho, Otávio R. Ahooja, Vineeta Deva, Djeven P. Garg, Vinay Gandhi, Sumeet Connelly, Kim A. Yan, Andrew T. Cardiovasc Diabetol Original Investigation BACKGROUND: Sodium-glucose cotransporter 2 (SGLT2) inhibition reduces cardiovascular events in type 2 diabetes (T2DM) and is associated with a reduction in left ventricular (LV) mass index. However, the impact on right ventricular (RV) remodeling is unknown. Accordingly, the objective of this study was to assess the impact of SGLT2 inhibition on RV parameters and function in T2DM and coronary artery disease (CAD). METHODS: In EMPA-HEART CardioLink-6, 97 patients with T2DM and CAD were randomly assigned to empagliflozin 10 mg (n = 49) once daily or placebo (n = 48). Cardiac magnetic resonance imaging was performed at baseline and after 6 months. RV mass index (RVMi), RV end-diastolic and end-systolic volume index (RVEDVi, RVESVi) and RV ejection fraction (RVEF) were assessed in blinded fashion. RESULTS: At baseline, mean RVMi (± SD) (11.8 ± 2.4 g/m(2)), RVEF (53.5 ± 4.8%), RVEDVi (64.3 ± 13.2 mL/m(2)) and RVESVi (29.9 ± 6.9 mL/m(2)) were within normal limits and were similar between the empagliflozin and placebo groups. Over 6 months, there were no significant differences in RVMi (− 0.11 g/m(2), [95% CI − 0.81 to 0.60], p = 0.76), RVEF (0.54%, [95% CI − 1.4 to 2.4], p = 0.58), RVEDVi (− 1.2 mL/m(2), [95% CI − 4.1 to 1.7], p = 0.41) and RVESVi (− 0.81 mL/m(2), [95% CI − 2.5 to 0.90], p = 0.35) in the empaglifozin group as compared with the placebo group. In both groups, there was no significant correlation between RVMi and LVMi changes from baseline to 6 months. CONCLUSIONS: In this post-hoc analysis, SGLT2 inhibition with empagliflozin had no impact on RVMi and RV volumes in patients with T2DM and CAD. The potentially differential effect of empagliflozin on the LV and RV warrants further investigation. Clinical Trial Registration: URL: https://www.clinicaltrials.gov/ct2/show/NCT02998970?cond=NCT02998970&draw=2&rank=1. Unique identifier: NCT02998970. BioMed Central 2021-10-04 /pmc/articles/PMC8491405/ /pubmed/34607574 http://dx.doi.org/10.1186/s12933-021-01390-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Investigation
Sarak, Bradley
Verma, Subodh
David Mazer, C.
Teoh, Hwee
Quan, Adrian
Gilbert, Richard E.
Goodman, Shaun G.
Bami, Karan
Coelho-Filho, Otávio R.
Ahooja, Vineeta
Deva, Djeven P.
Garg, Vinay
Gandhi, Sumeet
Connelly, Kim A.
Yan, Andrew T.
Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title_full Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title_fullStr Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title_full_unstemmed Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title_short Impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
title_sort impact of empagliflozin on right ventricular parameters and function among patients with type 2 diabetes
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491405/
https://www.ncbi.nlm.nih.gov/pubmed/34607574
http://dx.doi.org/10.1186/s12933-021-01390-8
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