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CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy

AIMS: CMR feature tracking strain (CMR-FT) provides prognostic information. However, there is a paucity of data in hypertrophic cardiomyopathy (HCM). We sought to analyze global CMR-FT parameters in all four cardiac chambers and to assess associations with NT-proBNP and cardiac troponin T (hsTnT) in...

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Autores principales: Cavus, Ersin, Muellerleile, Kai, Schellert, Samuel, Schneider, Jan, Tahir, Enver, Chevalier, Celeste, Jahnke, Charlotte, Radunski, Ulf K., Adam, Gerhard, Kirchhof, Paulus, Blankenberg, Stefan, Lund, Gunnar K., Avanesov, Maxim, Patten, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563550/
https://www.ncbi.nlm.nih.gov/pubmed/33779809
http://dx.doi.org/10.1007/s00392-021-01848-5
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author Cavus, Ersin
Muellerleile, Kai
Schellert, Samuel
Schneider, Jan
Tahir, Enver
Chevalier, Celeste
Jahnke, Charlotte
Radunski, Ulf K.
Adam, Gerhard
Kirchhof, Paulus
Blankenberg, Stefan
Lund, Gunnar K.
Avanesov, Maxim
Patten, Monica
author_facet Cavus, Ersin
Muellerleile, Kai
Schellert, Samuel
Schneider, Jan
Tahir, Enver
Chevalier, Celeste
Jahnke, Charlotte
Radunski, Ulf K.
Adam, Gerhard
Kirchhof, Paulus
Blankenberg, Stefan
Lund, Gunnar K.
Avanesov, Maxim
Patten, Monica
author_sort Cavus, Ersin
collection PubMed
description AIMS: CMR feature tracking strain (CMR-FT) provides prognostic information. However, there is a paucity of data in hypertrophic cardiomyopathy (HCM). We sought to analyze global CMR-FT parameters in all four cardiac chambers and to assess associations with NT-proBNP and cardiac troponin T (hsTnT) in patients with HCM. METHODS: This retrospective study included 144 HCM patients and 16 healthy controls with CMR at 1.5 T. Analyses were performed on standard steady-state free precession cine (SSFP) CMR data using a commercially available software. Global left ventricular (LV) strain was assessed as longitudinal (LV(LAX-)GLS), circumferential (LV(LAX-)GCS) and radial strain (LV(LAX-)GRS) on long -axis (LAX) and as LV(SAX)-GCS and LV(SAX)-GRS on short- axis (SAX). Right ventricular (RV-GLS), left atrial (LA-GLS) and right atrial (RA-GLS) strain were assessed on LAX. RESULTS: We found LV(LAX)-GLS [− 18.9 (− 22.0, − 16.0), − 23.5 (− 25.5, − 22.0) %, p = 0.0001), LV(SAX)-GRS [86.8 (65.9–115.5), 119.6 (91.3–143.7) %, p = 0.001] and LA(LAX)-GLS [LA(2CH)-GLS 29.2 (19.1–37.7), LA(2CH)-GLS 38.2 (34.3–47.1) %, p = 0.0036; LA(4CH)-GLS 22.4 (14.6–30.7) vs. LA(4CH)-GLS 33.4 (28.4–37.3) %, p = 0.0033] to be impaired in HCM compared to healthy controls despite normal LVEF. Furthermore, LV and LA strain parameters were impaired in HCM with elevated NT-proBNP and/or hsTnT, despite preserved LVEF compared to HCM with normal biomarker levels. There was a moderate correlation of LV and LA CMR-FT with levels of NT-proBNP and hsTnT. CONCLUSION: CMR-FT reveals LV and LA dysfunction in HCM despite normal LVEF. The association between impaired LV strain and elevated NT-proBNP and hsTnT indicates a link between unapparent functional abnormalities and disease severity in HCM. GRAPHIC ABSTRACT: Typical CMR-FT findings in patients with hypertrophic cardiomyopathy [Image: see text]
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spelling pubmed-85635502021-11-04 CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy Cavus, Ersin Muellerleile, Kai Schellert, Samuel Schneider, Jan Tahir, Enver Chevalier, Celeste Jahnke, Charlotte Radunski, Ulf K. Adam, Gerhard Kirchhof, Paulus Blankenberg, Stefan Lund, Gunnar K. Avanesov, Maxim Patten, Monica Clin Res Cardiol Original Paper AIMS: CMR feature tracking strain (CMR-FT) provides prognostic information. However, there is a paucity of data in hypertrophic cardiomyopathy (HCM). We sought to analyze global CMR-FT parameters in all four cardiac chambers and to assess associations with NT-proBNP and cardiac troponin T (hsTnT) in patients with HCM. METHODS: This retrospective study included 144 HCM patients and 16 healthy controls with CMR at 1.5 T. Analyses were performed on standard steady-state free precession cine (SSFP) CMR data using a commercially available software. Global left ventricular (LV) strain was assessed as longitudinal (LV(LAX-)GLS), circumferential (LV(LAX-)GCS) and radial strain (LV(LAX-)GRS) on long -axis (LAX) and as LV(SAX)-GCS and LV(SAX)-GRS on short- axis (SAX). Right ventricular (RV-GLS), left atrial (LA-GLS) and right atrial (RA-GLS) strain were assessed on LAX. RESULTS: We found LV(LAX)-GLS [− 18.9 (− 22.0, − 16.0), − 23.5 (− 25.5, − 22.0) %, p = 0.0001), LV(SAX)-GRS [86.8 (65.9–115.5), 119.6 (91.3–143.7) %, p = 0.001] and LA(LAX)-GLS [LA(2CH)-GLS 29.2 (19.1–37.7), LA(2CH)-GLS 38.2 (34.3–47.1) %, p = 0.0036; LA(4CH)-GLS 22.4 (14.6–30.7) vs. LA(4CH)-GLS 33.4 (28.4–37.3) %, p = 0.0033] to be impaired in HCM compared to healthy controls despite normal LVEF. Furthermore, LV and LA strain parameters were impaired in HCM with elevated NT-proBNP and/or hsTnT, despite preserved LVEF compared to HCM with normal biomarker levels. There was a moderate correlation of LV and LA CMR-FT with levels of NT-proBNP and hsTnT. CONCLUSION: CMR-FT reveals LV and LA dysfunction in HCM despite normal LVEF. The association between impaired LV strain and elevated NT-proBNP and hsTnT indicates a link between unapparent functional abnormalities and disease severity in HCM. GRAPHIC ABSTRACT: Typical CMR-FT findings in patients with hypertrophic cardiomyopathy [Image: see text] Springer Berlin Heidelberg 2021-03-29 2021 /pmc/articles/PMC8563550/ /pubmed/33779809 http://dx.doi.org/10.1007/s00392-021-01848-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Paper
Cavus, Ersin
Muellerleile, Kai
Schellert, Samuel
Schneider, Jan
Tahir, Enver
Chevalier, Celeste
Jahnke, Charlotte
Radunski, Ulf K.
Adam, Gerhard
Kirchhof, Paulus
Blankenberg, Stefan
Lund, Gunnar K.
Avanesov, Maxim
Patten, Monica
CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title_full CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title_fullStr CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title_full_unstemmed CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title_short CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
title_sort cmr feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with hypertrophic cardiomyopathy
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563550/
https://www.ncbi.nlm.nih.gov/pubmed/33779809
http://dx.doi.org/10.1007/s00392-021-01848-5
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