Cargando…

Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy

AIMS: This study aims to assess subclinical changes in functional and morphological myocardial magnetic resonance parameters very early into an anthracycline treatment, which may predict subsequent development of anthracycline‐induced cardiomyopathy (aCMP). METHODS AND RESULTS: Thirty sarcoma patien...

Descripción completa

Detalles Bibliográficos
Autores principales: Muehlberg, Fabian, Funk, Stephanie, Zange, Leonora, von Knobelsdorff‐Brenkenhoff, Florian, Blaszczyk, Edyta, Schulz, Alexander, Ghani, Saeed, Reichardt, Annete, Reichardt, Peter, Schulz‐Menger, Jeanette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073029/
https://www.ncbi.nlm.nih.gov/pubmed/29673122
http://dx.doi.org/10.1002/ehf2.12277
_version_ 1783344101724258304
author Muehlberg, Fabian
Funk, Stephanie
Zange, Leonora
von Knobelsdorff‐Brenkenhoff, Florian
Blaszczyk, Edyta
Schulz, Alexander
Ghani, Saeed
Reichardt, Annete
Reichardt, Peter
Schulz‐Menger, Jeanette
author_facet Muehlberg, Fabian
Funk, Stephanie
Zange, Leonora
von Knobelsdorff‐Brenkenhoff, Florian
Blaszczyk, Edyta
Schulz, Alexander
Ghani, Saeed
Reichardt, Annete
Reichardt, Peter
Schulz‐Menger, Jeanette
author_sort Muehlberg, Fabian
collection PubMed
description AIMS: This study aims to assess subclinical changes in functional and morphological myocardial magnetic resonance parameters very early into an anthracycline treatment, which may predict subsequent development of anthracycline‐induced cardiomyopathy (aCMP). METHODS AND RESULTS: Thirty sarcoma patients with planned anthracycline‐based chemotherapy (360–400 mg/m(2) doxorubicin‐equivalent) were recruited. Median treatment time was 19.1 ± 2.1 weeks. Enrolled individuals received three cardiovascular magnetic resonance studies (before treatment, 48 h after first anthracycline treatment, and upon completion of treatment). Native T1 mapping (modified Look–Locker inversion recovery 5s(3s)3s), T2 mapping, and extracellular volume maps were acquired in addition to a conventional cardiovascular magnetic resonance with steady‐state free precession cine imaging at 1.5 T. Patients were given 0.2 mmol/kg gadoteridol for extracellular volume quantification and late gadolinium enhancement imaging. Development of relevant aCMP was defined as drop of left ventricular ejection fraction (LVEF) by >10%. For analysis, 23 complete data sets were available. Nine patients developed aCMP with LVEF reduction >10% until end of chemotherapy. Baseline LVEF was not different between patients with and without subsequent aCMP. When assessed 48 h after first dose of antracyclines, patients with subsequent aCMP had significantly lower native myocardial T1 times compared with before therapy (1002.0 ± 37.9 vs. 956.5 ± 29.2 ms, P < 0.01) than patients who did not develop aCMP (990.9 ± 56.4 vs. 978.4 ± 57.4 ms, P > 0.05). Patients with aCMP had decreased left ventricular mass upon completion of therapy (86.9 ± 24.5 vs. 81.1 ± 22.3 g; P = 0.02), while patients without aCMP did not show a change in left ventricular mass (81.8 ± 21.0 vs. 79.2 ± 18.1 g; P > 0.05). No patient developed new myocardial scars or compact myocardial fibrosis under chemotherapy. CONCLUSIONS: Early decrease of T1 times 48 h after first treatment with anthracyclines can predict the development of subsequent aCMP after completion of chemotherapy.
format Online
Article
Text
id pubmed-6073029
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-60730292018-08-07 Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy Muehlberg, Fabian Funk, Stephanie Zange, Leonora von Knobelsdorff‐Brenkenhoff, Florian Blaszczyk, Edyta Schulz, Alexander Ghani, Saeed Reichardt, Annete Reichardt, Peter Schulz‐Menger, Jeanette ESC Heart Fail Original Research Articles AIMS: This study aims to assess subclinical changes in functional and morphological myocardial magnetic resonance parameters very early into an anthracycline treatment, which may predict subsequent development of anthracycline‐induced cardiomyopathy (aCMP). METHODS AND RESULTS: Thirty sarcoma patients with planned anthracycline‐based chemotherapy (360–400 mg/m(2) doxorubicin‐equivalent) were recruited. Median treatment time was 19.1 ± 2.1 weeks. Enrolled individuals received three cardiovascular magnetic resonance studies (before treatment, 48 h after first anthracycline treatment, and upon completion of treatment). Native T1 mapping (modified Look–Locker inversion recovery 5s(3s)3s), T2 mapping, and extracellular volume maps were acquired in addition to a conventional cardiovascular magnetic resonance with steady‐state free precession cine imaging at 1.5 T. Patients were given 0.2 mmol/kg gadoteridol for extracellular volume quantification and late gadolinium enhancement imaging. Development of relevant aCMP was defined as drop of left ventricular ejection fraction (LVEF) by >10%. For analysis, 23 complete data sets were available. Nine patients developed aCMP with LVEF reduction >10% until end of chemotherapy. Baseline LVEF was not different between patients with and without subsequent aCMP. When assessed 48 h after first dose of antracyclines, patients with subsequent aCMP had significantly lower native myocardial T1 times compared with before therapy (1002.0 ± 37.9 vs. 956.5 ± 29.2 ms, P < 0.01) than patients who did not develop aCMP (990.9 ± 56.4 vs. 978.4 ± 57.4 ms, P > 0.05). Patients with aCMP had decreased left ventricular mass upon completion of therapy (86.9 ± 24.5 vs. 81.1 ± 22.3 g; P = 0.02), while patients without aCMP did not show a change in left ventricular mass (81.8 ± 21.0 vs. 79.2 ± 18.1 g; P > 0.05). No patient developed new myocardial scars or compact myocardial fibrosis under chemotherapy. CONCLUSIONS: Early decrease of T1 times 48 h after first treatment with anthracyclines can predict the development of subsequent aCMP after completion of chemotherapy. John Wiley and Sons Inc. 2018-04-19 /pmc/articles/PMC6073029/ /pubmed/29673122 http://dx.doi.org/10.1002/ehf2.12277 Text en © 2018 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the http://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 Original Research Articles
Muehlberg, Fabian
Funk, Stephanie
Zange, Leonora
von Knobelsdorff‐Brenkenhoff, Florian
Blaszczyk, Edyta
Schulz, Alexander
Ghani, Saeed
Reichardt, Annete
Reichardt, Peter
Schulz‐Menger, Jeanette
Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title_full Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title_fullStr Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title_full_unstemmed Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title_short Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
title_sort native myocardial t1 time can predict development of subsequent anthracycline‐induced cardiomyopathy
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073029/
https://www.ncbi.nlm.nih.gov/pubmed/29673122
http://dx.doi.org/10.1002/ehf2.12277
work_keys_str_mv AT muehlbergfabian nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT funkstephanie nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT zangeleonora nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT vonknobelsdorffbrenkenhoffflorian nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT blaszczykedyta nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT schulzalexander nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT ghanisaeed nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT reichardtannete nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT reichardtpeter nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy
AT schulzmengerjeanette nativemyocardialt1timecanpredictdevelopmentofsubsequentanthracyclineinducedcardiomyopathy