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Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients

INTRODUCTION: Increased left atrial (LA) size is a risk factor for cardiovascular events and all-cause mortality. It is closely related to left ventricular hypertrophy and chronic volume overload, both of which are common in hemodialysis. Calcimimetic treatment with etelcalcetide (ETL) previously sh...

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Autores principales: Dörr, Katharina, Reindl-Schwaighofer, Roman, Lorenz, Matthias, Marculescu, Rodrig, Beitzke, Dietrich, Hödlmoser, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664324/
https://www.ncbi.nlm.nih.gov/pubmed/37729887
http://dx.doi.org/10.1159/000533899
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author Dörr, Katharina
Reindl-Schwaighofer, Roman
Lorenz, Matthias
Marculescu, Rodrig
Beitzke, Dietrich
Hödlmoser, Sebastian
author_facet Dörr, Katharina
Reindl-Schwaighofer, Roman
Lorenz, Matthias
Marculescu, Rodrig
Beitzke, Dietrich
Hödlmoser, Sebastian
author_sort Dörr, Katharina
collection PubMed
description INTRODUCTION: Increased left atrial (LA) size is a risk factor for cardiovascular events and all-cause mortality. It is closely related to left ventricular hypertrophy and chronic volume overload, both of which are common in hemodialysis. Calcimimetic treatment with etelcalcetide (ETL) previously showed an inhibitory effect on left ventricular mass index (LVMI) progression in this population. METHODS: This is a post hoc analysis of the EtECAR-HD trial, where 62 patients were randomized to ETL or alfacalcidol (ALFA) for 1 year. LA volume index (LAVI) was measured using cardiac magnetic resonance imaging. The aim of the study was to investigate whether ETL was associated with a change of LAVI. RESULTS: Median baseline levels of LAVI were 40 mL/m(2) (31, 54 IQR) in the ETL group and 36 mL/m(2) (26, 46 IQR) in the ALFA group. In the ITT population, the change of LAVI was 5.0 mL/m(2) [95% CI: −0.04, 10] lower under ETL, compared to ALFA (p = 0.052, R(2)(adj) = 0.259). In the PP population, the difference in LAVI changes widened to 5.8 [95% CI: 0.36, 11], p = 0.037, R(2)(adj) = 0.302). Secondary analysis showed that the study delta of LVMI was correlated with the LAVI delta (r = 0.387) and that an inclusion of LVMI delta in the ANCOVA model mediated the effect on LAVI delta to β = 3.3 [95% CI: −0.04, 10] (p = 0.2, R(2)(adj) = 0.323). The same could not be observed for parameters assessing the volume status. CONCLUSIONS: The analysis indicates that ETL could inhibit LAVI progression compared with ALFA. This effect was mediated by the change of LVMI.
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spelling pubmed-106643242023-09-20 Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients Dörr, Katharina Reindl-Schwaighofer, Roman Lorenz, Matthias Marculescu, Rodrig Beitzke, Dietrich Hödlmoser, Sebastian Cardiorenal Med Research Article INTRODUCTION: Increased left atrial (LA) size is a risk factor for cardiovascular events and all-cause mortality. It is closely related to left ventricular hypertrophy and chronic volume overload, both of which are common in hemodialysis. Calcimimetic treatment with etelcalcetide (ETL) previously showed an inhibitory effect on left ventricular mass index (LVMI) progression in this population. METHODS: This is a post hoc analysis of the EtECAR-HD trial, where 62 patients were randomized to ETL or alfacalcidol (ALFA) for 1 year. LA volume index (LAVI) was measured using cardiac magnetic resonance imaging. The aim of the study was to investigate whether ETL was associated with a change of LAVI. RESULTS: Median baseline levels of LAVI were 40 mL/m(2) (31, 54 IQR) in the ETL group and 36 mL/m(2) (26, 46 IQR) in the ALFA group. In the ITT population, the change of LAVI was 5.0 mL/m(2) [95% CI: −0.04, 10] lower under ETL, compared to ALFA (p = 0.052, R(2)(adj) = 0.259). In the PP population, the difference in LAVI changes widened to 5.8 [95% CI: 0.36, 11], p = 0.037, R(2)(adj) = 0.302). Secondary analysis showed that the study delta of LVMI was correlated with the LAVI delta (r = 0.387) and that an inclusion of LVMI delta in the ANCOVA model mediated the effect on LAVI delta to β = 3.3 [95% CI: −0.04, 10] (p = 0.2, R(2)(adj) = 0.323). The same could not be observed for parameters assessing the volume status. CONCLUSIONS: The analysis indicates that ETL could inhibit LAVI progression compared with ALFA. This effect was mediated by the change of LVMI. S. Karger AG 2023-09-20 /pmc/articles/PMC10664324/ /pubmed/37729887 http://dx.doi.org/10.1159/000533899 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Research Article
Dörr, Katharina
Reindl-Schwaighofer, Roman
Lorenz, Matthias
Marculescu, Rodrig
Beitzke, Dietrich
Hödlmoser, Sebastian
Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title_full Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title_fullStr Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title_full_unstemmed Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title_short Etelcalcetide Inhibits the Progression of Left Atrial Volume Index Compared to Alfacalcidol in Hemodialysis Patients
title_sort etelcalcetide inhibits the progression of left atrial volume index compared to alfacalcidol in hemodialysis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664324/
https://www.ncbi.nlm.nih.gov/pubmed/37729887
http://dx.doi.org/10.1159/000533899
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