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Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)

BACKGROUND: The p.Arg14del (c.40_42delAGA) phospholamban (PLN) pathogenic variant is a founder mutation that causes dilated cardiomyopathy (DCM) and arrhythmogenic cardiomyopathy (ACM). Carriers are at increased risk of malignant ventricular arrhythmias and heart failure, which has been ascribed to...

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Autores principales: te Rijdt, W. P., Hoorntje, E. T., de Brouwer, R., Oomen, A., Amin, A., van der Heijden, J. F., Karper, J. C., Westenbrink, B. D., Silljé, H. H. W., te Riele, A. S. J. M., Wiesfeld, A. C. P., van Gelder, I. C., Willems, T. P., van der Zwaag, P. A., van Tintelen, J. P., Hillege, J. H., Tan, H. L., van Veldhuisen, D. J., Asselbergs, F. W., de Boer, R. A., Wilde, A. A. M., van den Berg, M. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799798/
https://www.ncbi.nlm.nih.gov/pubmed/34143416
http://dx.doi.org/10.1007/s12471-021-01584-5
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author te Rijdt, W. P.
Hoorntje, E. T.
de Brouwer, R.
Oomen, A.
Amin, A.
van der Heijden, J. F.
Karper, J. C.
Westenbrink, B. D.
Silljé, H. H. W.
te Riele, A. S. J. M.
Wiesfeld, A. C. P.
van Gelder, I. C.
Willems, T. P.
van der Zwaag, P. A.
van Tintelen, J. P.
Hillege, J. H.
Tan, H. L.
van Veldhuisen, D. J.
Asselbergs, F. W.
de Boer, R. A.
Wilde, A. A. M.
van den Berg, M. P.
author_facet te Rijdt, W. P.
Hoorntje, E. T.
de Brouwer, R.
Oomen, A.
Amin, A.
van der Heijden, J. F.
Karper, J. C.
Westenbrink, B. D.
Silljé, H. H. W.
te Riele, A. S. J. M.
Wiesfeld, A. C. P.
van Gelder, I. C.
Willems, T. P.
van der Zwaag, P. A.
van Tintelen, J. P.
Hillege, J. H.
Tan, H. L.
van Veldhuisen, D. J.
Asselbergs, F. W.
de Boer, R. A.
Wilde, A. A. M.
van den Berg, M. P.
author_sort te Rijdt, W. P.
collection PubMed
description BACKGROUND: The p.Arg14del (c.40_42delAGA) phospholamban (PLN) pathogenic variant is a founder mutation that causes dilated cardiomyopathy (DCM) and arrhythmogenic cardiomyopathy (ACM). Carriers are at increased risk of malignant ventricular arrhythmias and heart failure, which has been ascribed to cardiac fibrosis. Importantly, cardiac fibrosis appears to be an early feature of the disease, occurring in many presymptomatic carriers before the onset of overt disease. As with most monogenic cardiomyopathies, no evidence-based treatment is available for presymptomatic carriers. AIMS: The PHOspholamban RElated CArdiomyopathy intervention STudy (iPHORECAST) is designed to demonstrate that pre-emptive treatment of presymptomatic PLN p.Arg14del carriers using eplerenone, a mineralocorticoid receptor antagonist with established antifibrotic effects, can reduce disease progression and postpone the onset of overt disease. METHODS: iPHORECAST has a multicentre, prospective, randomised, open-label, blinded endpoint (PROBE) design. Presymptomatic PLN p.Arg14del carriers are randomised to receive either 50 mg eplerenone once daily or no treatment. The primary endpoint of the study is a multiparametric assessment of disease progression including cardiac magnetic resonance parameters (left and right ventricular volumes, systolic function and fibrosis), electrocardiographic parameters (QRS voltage, ventricular ectopy), signs and/or symptoms related to DCM and ACM, and cardiovascular death. The follow-up duration is set at 3 years. BASELINE RESULTS: A total of 84 presymptomatic PLN p.Arg14del carriers (n = 42 per group) were included. By design, at baseline, all participants were in New York Heart Association (NHYA) class I and had a left ventricular ejection fraction > 45% and < 2500 ventricular premature contractions during 24-hour Holter monitoring. There were no statistically significant differences between the two groups in any of the baseline characteristics. The study is currently well underway, with the last participants expected to finish in 2021. CONCLUSION: iPHORECAST is a multicentre, prospective randomised controlled trial designed to address whether pre-emptive treatment of PLN p.Arg14del carriers with eplerenone can prevent or delay the onset of cardiomyopathy. iPHORECAST has been registered in the clinicaltrials.gov-register (number: NCT01857856).
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spelling pubmed-87997982022-02-02 Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST) te Rijdt, W. P. Hoorntje, E. T. de Brouwer, R. Oomen, A. Amin, A. van der Heijden, J. F. Karper, J. C. Westenbrink, B. D. Silljé, H. H. W. te Riele, A. S. J. M. Wiesfeld, A. C. P. van Gelder, I. C. Willems, T. P. van der Zwaag, P. A. van Tintelen, J. P. Hillege, J. H. Tan, H. L. van Veldhuisen, D. J. Asselbergs, F. W. de Boer, R. A. Wilde, A. A. M. van den Berg, M. P. Neth Heart J Original Article – Study Design Article BACKGROUND: The p.Arg14del (c.40_42delAGA) phospholamban (PLN) pathogenic variant is a founder mutation that causes dilated cardiomyopathy (DCM) and arrhythmogenic cardiomyopathy (ACM). Carriers are at increased risk of malignant ventricular arrhythmias and heart failure, which has been ascribed to cardiac fibrosis. Importantly, cardiac fibrosis appears to be an early feature of the disease, occurring in many presymptomatic carriers before the onset of overt disease. As with most monogenic cardiomyopathies, no evidence-based treatment is available for presymptomatic carriers. AIMS: The PHOspholamban RElated CArdiomyopathy intervention STudy (iPHORECAST) is designed to demonstrate that pre-emptive treatment of presymptomatic PLN p.Arg14del carriers using eplerenone, a mineralocorticoid receptor antagonist with established antifibrotic effects, can reduce disease progression and postpone the onset of overt disease. METHODS: iPHORECAST has a multicentre, prospective, randomised, open-label, blinded endpoint (PROBE) design. Presymptomatic PLN p.Arg14del carriers are randomised to receive either 50 mg eplerenone once daily or no treatment. The primary endpoint of the study is a multiparametric assessment of disease progression including cardiac magnetic resonance parameters (left and right ventricular volumes, systolic function and fibrosis), electrocardiographic parameters (QRS voltage, ventricular ectopy), signs and/or symptoms related to DCM and ACM, and cardiovascular death. The follow-up duration is set at 3 years. BASELINE RESULTS: A total of 84 presymptomatic PLN p.Arg14del carriers (n = 42 per group) were included. By design, at baseline, all participants were in New York Heart Association (NHYA) class I and had a left ventricular ejection fraction > 45% and < 2500 ventricular premature contractions during 24-hour Holter monitoring. There were no statistically significant differences between the two groups in any of the baseline characteristics. The study is currently well underway, with the last participants expected to finish in 2021. CONCLUSION: iPHORECAST is a multicentre, prospective randomised controlled trial designed to address whether pre-emptive treatment of PLN p.Arg14del carriers with eplerenone can prevent or delay the onset of cardiomyopathy. iPHORECAST has been registered in the clinicaltrials.gov-register (number: NCT01857856). Bohn Stafleu van Loghum 2021-06-18 2022-02 /pmc/articles/PMC8799798/ /pubmed/34143416 http://dx.doi.org/10.1007/s12471-021-01584-5 Text en © The Author(s) 2021 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/) .
spellingShingle Original Article – Study Design Article
te Rijdt, W. P.
Hoorntje, E. T.
de Brouwer, R.
Oomen, A.
Amin, A.
van der Heijden, J. F.
Karper, J. C.
Westenbrink, B. D.
Silljé, H. H. W.
te Riele, A. S. J. M.
Wiesfeld, A. C. P.
van Gelder, I. C.
Willems, T. P.
van der Zwaag, P. A.
van Tintelen, J. P.
Hillege, J. H.
Tan, H. L.
van Veldhuisen, D. J.
Asselbergs, F. W.
de Boer, R. A.
Wilde, A. A. M.
van den Berg, M. P.
Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title_full Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title_fullStr Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title_full_unstemmed Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title_short Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
title_sort rationale and design of the phospholamban related cardiomyopathy intervention study (i-phorecast)
topic Original Article – Study Design Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799798/
https://www.ncbi.nlm.nih.gov/pubmed/34143416
http://dx.doi.org/10.1007/s12471-021-01584-5
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