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Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping

Diffuse myocardial fibrosis is a key pathophysiologic feature in heart failure and can be quantified by cardiac magnetic resonance (CMR) T1 mapping. However, increases in myocardial free water also prolong native T1 times and may impact fibrosis quantification. Thus far, the impact of systemic patie...

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Autores principales: Antlanger, Marlies, Aschauer, Stefan, Kammerlander, Andreas A., Duca, Franz, Säemann, Marcus D., Bonderman, Diana, Mascherbauer, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882796/
https://www.ncbi.nlm.nih.gov/pubmed/29615750
http://dx.doi.org/10.1038/s41598-018-23868-4
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author Antlanger, Marlies
Aschauer, Stefan
Kammerlander, Andreas A.
Duca, Franz
Säemann, Marcus D.
Bonderman, Diana
Mascherbauer, Julia
author_facet Antlanger, Marlies
Aschauer, Stefan
Kammerlander, Andreas A.
Duca, Franz
Säemann, Marcus D.
Bonderman, Diana
Mascherbauer, Julia
author_sort Antlanger, Marlies
collection PubMed
description Diffuse myocardial fibrosis is a key pathophysiologic feature in heart failure and can be quantified by cardiac magnetic resonance (CMR) T1 mapping. However, increases in myocardial free water also prolong native T1 times and may impact fibrosis quantification. Thus far, the impact of systemic patient volume status remains unclear. In this study, native T1 time by CMR was investigated in hemodialysis (HD) patients (n = 37) and compared with healthy controls (n = 35). Volume status was quantified by bioimpedance spectroscopy and correlated with CMR T1 time. While no differences between HD patients and controls were present with regard to age (p = 0.180), height (p = 0.535), weight (p = 0.559) and left ventricular (LV) ejection fraction (p = 0.273), cardiac size was significantly larger in HD patients (LV end-diastolic volume 164 ± 53 vs. 132 ± 26 ml, p = 0.002). Fluid overloaded HD patients had significantly longer native T1 times than normovolemic HD patients and healthy controls (1,042 ± 46 vs. 1,005 ± 49 vs. 998 ± 47 ms, p = 0.030). By regression analysis, T1 time was significantly associated with fluid status (r = 0.530, p = 0.009, post-HD fluid status). Our data strongly indicate that native CMR T1 time is significantly influenced by systemic volume status. As fluid overload is common in patients with cardiovascular diseases, this finding is important and requires further study.
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spelling pubmed-58827962018-04-09 Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping Antlanger, Marlies Aschauer, Stefan Kammerlander, Andreas A. Duca, Franz Säemann, Marcus D. Bonderman, Diana Mascherbauer, Julia Sci Rep Article Diffuse myocardial fibrosis is a key pathophysiologic feature in heart failure and can be quantified by cardiac magnetic resonance (CMR) T1 mapping. However, increases in myocardial free water also prolong native T1 times and may impact fibrosis quantification. Thus far, the impact of systemic patient volume status remains unclear. In this study, native T1 time by CMR was investigated in hemodialysis (HD) patients (n = 37) and compared with healthy controls (n = 35). Volume status was quantified by bioimpedance spectroscopy and correlated with CMR T1 time. While no differences between HD patients and controls were present with regard to age (p = 0.180), height (p = 0.535), weight (p = 0.559) and left ventricular (LV) ejection fraction (p = 0.273), cardiac size was significantly larger in HD patients (LV end-diastolic volume 164 ± 53 vs. 132 ± 26 ml, p = 0.002). Fluid overloaded HD patients had significantly longer native T1 times than normovolemic HD patients and healthy controls (1,042 ± 46 vs. 1,005 ± 49 vs. 998 ± 47 ms, p = 0.030). By regression analysis, T1 time was significantly associated with fluid status (r = 0.530, p = 0.009, post-HD fluid status). Our data strongly indicate that native CMR T1 time is significantly influenced by systemic volume status. As fluid overload is common in patients with cardiovascular diseases, this finding is important and requires further study. Nature Publishing Group UK 2018-04-03 /pmc/articles/PMC5882796/ /pubmed/29615750 http://dx.doi.org/10.1038/s41598-018-23868-4 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Antlanger, Marlies
Aschauer, Stefan
Kammerlander, Andreas A.
Duca, Franz
Säemann, Marcus D.
Bonderman, Diana
Mascherbauer, Julia
Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title_full Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title_fullStr Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title_full_unstemmed Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title_short Impact of Systemic Volume Status on Cardiac Magnetic Resonance T1 Mapping
title_sort impact of systemic volume status on cardiac magnetic resonance t1 mapping
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882796/
https://www.ncbi.nlm.nih.gov/pubmed/29615750
http://dx.doi.org/10.1038/s41598-018-23868-4
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