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Impact of diabetes duration on left ventricular mass regression with empagliflozin
AIMS: The duration of type 2 diabetes mellitus (T2DM) is an important determinant of diabetes severity. The EMPA‐HEART CardioLink‐6 trial reported significant left ventricular (LV) mass indexed to body surface area (LVMi) regression in patients treated with the sodium‐glucose cotransporter 2 inhibit...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192246/ https://www.ncbi.nlm.nih.gov/pubmed/37038614 http://dx.doi.org/10.1002/ehf2.14357 |
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author | Moroney, Michael Verma, Raj Hibino, Makoto Mazer, C. David Connelly, Kim A. Yan, Andrew T. Quan, Adrian Teoh, Hwee Verma, Subodh Puar, Pankaj |
author_facet | Moroney, Michael Verma, Raj Hibino, Makoto Mazer, C. David Connelly, Kim A. Yan, Andrew T. Quan, Adrian Teoh, Hwee Verma, Subodh Puar, Pankaj |
author_sort | Moroney, Michael |
collection | PubMed |
description | AIMS: The duration of type 2 diabetes mellitus (T2DM) is an important determinant of diabetes severity. The EMPA‐HEART CardioLink‐6 trial reported significant left ventricular (LV) mass indexed to body surface area (LVMi) regression in patients treated with the sodium‐glucose cotransporter 2 inhibitor (SGLT2i) empagliflozin for 6 months. This exploratory sub‐analysis of the same trial investigated the association between T2DM duration and LVMi regression. METHODS AND RESULTS: A total of 97 individuals with T2DM and coronary artery disease (CAD) were randomly assigned to receive empagliflozin 10 mg daily or placebo. LVMi was measured at the baseline and 6 month visit using cardiac magnetic resonance imaging. The study population was divided into those with a baseline T2DM duration <10 years (n = 40) or ≥10 years (n = 57). A linear model adjusting for baseline values in each of the subgroups (ANCOVA) was used to assess the treatment effect of 6 month change in LVMi, LV end systolic volume indexed to body surface area, LV end diastolic volume indexed to body surface area and LV ejection fraction. Patients in the T2DM duration <10 years group (38 males [95.0%], median age 63 [IQR: 55 years to 70 years]) had a median T2DM duration of 4 years (IQR: 2.0 years to 7.0 years). Those in the T2DM duration ≥10 years group (52 males [91.2%], median age 65 [IQR: 57 years to 71 years]) had a median duration of 15 years (IQR: 12 years to 20 years). There was no significant difference in baseline LVMi according to T2DM duration (median 62 g/m(2) [IQR: 53.1 g/m(2) to 70.0 g/m(2)] for T2DM duration <10 years; median 57.5 g/m(2) [IQR: 52.1 g/m(2) to 66.2 g/m(2)] for T2DM duration ≥10 years; P = 0.11). Empagliflozin was associated with reductions in LVMi irrespective of duration of T2DM above and below 10 years (T2DM duration <10 years group, mean adjusted difference −2.90 g/m(2) [95% CI: −6.64 g/m(2) to 0.84 g/m(2)]; T2DM duration ≥10 years group, mean adjusted difference −3.69 g/m(2) [95% CI: −0.14 g/m(2) to −7.24 g/m(2)]; P (interaction) = 0.07). CONCLUSIONS: In the EMPA‐HEART CardioLink‐6 trial, empagliflozin treatment was associated with reductions in LVMi in people with T2DM and CAD irrespective of the duration of diabetes assessed categorically above and below 10 years. |
format | Online Article Text |
id | pubmed-10192246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101922462023-05-19 Impact of diabetes duration on left ventricular mass regression with empagliflozin Moroney, Michael Verma, Raj Hibino, Makoto Mazer, C. David Connelly, Kim A. Yan, Andrew T. Quan, Adrian Teoh, Hwee Verma, Subodh Puar, Pankaj ESC Heart Fail Short Communications AIMS: The duration of type 2 diabetes mellitus (T2DM) is an important determinant of diabetes severity. The EMPA‐HEART CardioLink‐6 trial reported significant left ventricular (LV) mass indexed to body surface area (LVMi) regression in patients treated with the sodium‐glucose cotransporter 2 inhibitor (SGLT2i) empagliflozin for 6 months. This exploratory sub‐analysis of the same trial investigated the association between T2DM duration and LVMi regression. METHODS AND RESULTS: A total of 97 individuals with T2DM and coronary artery disease (CAD) were randomly assigned to receive empagliflozin 10 mg daily or placebo. LVMi was measured at the baseline and 6 month visit using cardiac magnetic resonance imaging. The study population was divided into those with a baseline T2DM duration <10 years (n = 40) or ≥10 years (n = 57). A linear model adjusting for baseline values in each of the subgroups (ANCOVA) was used to assess the treatment effect of 6 month change in LVMi, LV end systolic volume indexed to body surface area, LV end diastolic volume indexed to body surface area and LV ejection fraction. Patients in the T2DM duration <10 years group (38 males [95.0%], median age 63 [IQR: 55 years to 70 years]) had a median T2DM duration of 4 years (IQR: 2.0 years to 7.0 years). Those in the T2DM duration ≥10 years group (52 males [91.2%], median age 65 [IQR: 57 years to 71 years]) had a median duration of 15 years (IQR: 12 years to 20 years). There was no significant difference in baseline LVMi according to T2DM duration (median 62 g/m(2) [IQR: 53.1 g/m(2) to 70.0 g/m(2)] for T2DM duration <10 years; median 57.5 g/m(2) [IQR: 52.1 g/m(2) to 66.2 g/m(2)] for T2DM duration ≥10 years; P = 0.11). Empagliflozin was associated with reductions in LVMi irrespective of duration of T2DM above and below 10 years (T2DM duration <10 years group, mean adjusted difference −2.90 g/m(2) [95% CI: −6.64 g/m(2) to 0.84 g/m(2)]; T2DM duration ≥10 years group, mean adjusted difference −3.69 g/m(2) [95% CI: −0.14 g/m(2) to −7.24 g/m(2)]; P (interaction) = 0.07). CONCLUSIONS: In the EMPA‐HEART CardioLink‐6 trial, empagliflozin treatment was associated with reductions in LVMi in people with T2DM and CAD irrespective of the duration of diabetes assessed categorically above and below 10 years. John Wiley and Sons Inc. 2023-04-10 /pmc/articles/PMC10192246/ /pubmed/37038614 http://dx.doi.org/10.1002/ehf2.14357 Text en © 2023 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Communications Moroney, Michael Verma, Raj Hibino, Makoto Mazer, C. David Connelly, Kim A. Yan, Andrew T. Quan, Adrian Teoh, Hwee Verma, Subodh Puar, Pankaj Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title | Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title_full | Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title_fullStr | Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title_full_unstemmed | Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title_short | Impact of diabetes duration on left ventricular mass regression with empagliflozin |
title_sort | impact of diabetes duration on left ventricular mass regression with empagliflozin |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192246/ https://www.ncbi.nlm.nih.gov/pubmed/37038614 http://dx.doi.org/10.1002/ehf2.14357 |
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