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Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle

BACKGROUND: Adults with a systemic right ventricle (sRV) have a high risk of cardiac complications. This study aimed to identify prognostic markers in adults with sRV based on clinical evaluation, echocardiography, and blood biomarkers. METHODS AND RESULTS: In this prospective cohort study, consecut...

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Autores principales: Geenen, Laurie W., van Grootel, Roderick W. J., Akman, Korhan, Baggen, Vivan J. M., Menting, Myrthe E., Eindhoven, Jannet A., Cuypers, Judith A. A. E., Boersma, Eric, van den Bosch, Annemien E., Roos‐Hesselink, Jolien W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755830/
https://www.ncbi.nlm.nih.gov/pubmed/31431113
http://dx.doi.org/10.1161/JAHA.119.013745
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author Geenen, Laurie W.
van Grootel, Roderick W. J.
Akman, Korhan
Baggen, Vivan J. M.
Menting, Myrthe E.
Eindhoven, Jannet A.
Cuypers, Judith A. A. E.
Boersma, Eric
van den Bosch, Annemien E.
Roos‐Hesselink, Jolien W.
author_facet Geenen, Laurie W.
van Grootel, Roderick W. J.
Akman, Korhan
Baggen, Vivan J. M.
Menting, Myrthe E.
Eindhoven, Jannet A.
Cuypers, Judith A. A. E.
Boersma, Eric
van den Bosch, Annemien E.
Roos‐Hesselink, Jolien W.
author_sort Geenen, Laurie W.
collection PubMed
description BACKGROUND: Adults with a systemic right ventricle (sRV) have a high risk of cardiac complications. This study aimed to identify prognostic markers in adults with sRV based on clinical evaluation, echocardiography, and blood biomarkers. METHODS AND RESULTS: In this prospective cohort study, consecutive clinically stable adults with sRV caused by Mustard‐ or congenitally corrected transposition of the great arteries were included (2011–2013). Eighty‐six patients were included (age 37±9 years, 65% male, 83% New York Heart Association functional class I, 76% Mustard transposition of the great arteries, 24% congenitally corrected transposition of the great arteries). Venous blood sampling was performed including N‐terminal pro B‐type natriuretic peptide, high‐sensitive‐troponin‐T, high‐sensitivity C‐reactive protein, growth differentiation factor‐15, galectin‐3, red cell distribution width, estimated glomerular filtration rate, and hemoglobin. Besides conventional echocardiographic measurements, longitudinal, circumferential, and radial strain were assessed using strain analysis. During a median follow‐up of 5.9 (interquartile range 5.3–6.3) years, 19 (22%) patients died or had heart failure (primary end point) and 29 (34%) patients died or had arrhythmia (secondary end point). Univariable Cox regression analysis was performed using dichotomous or standardized continuous variables. New York Heart Association functional class >I, systolic blood pressure, and most blood biomarkers were associated with the primary and secondary end point (galectin‐3 not for primary, N‐terminal pro B‐type natriuretic peptide and high‐sensitivity C‐reactive protein not for secondary end point). Growth differentiation factor‐15 showed the strongest association with both end points (hazard ratios; 2.44 [95% CI 1.67–3.57, P<0.001], 2.00 [95% CI 1.46–2.73, P<0.001], respectively). End‐diastolic basal dimension of the subpulmonary ventricle was associated with both end points (hazard ratio: 1.95 [95% CI 1.34–2.85], P<0.001, 1.70 [95% CI 1.21–2.38, P=0.002], respectively). Concerning strain analysis, only sRV septal strain was associated with the secondary end point (hazard ratio 0.58 [95% CI 0.39–0.86], P=0.006). CONCLUSIONS: Clinical, conventional echocardiographic, and blood measurements are important markers for risk stratification in adults with a sRV. The value of novel echocardiographic strain analysis seems limited.
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spelling pubmed-67558302019-09-26 Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle Geenen, Laurie W. van Grootel, Roderick W. J. Akman, Korhan Baggen, Vivan J. M. Menting, Myrthe E. Eindhoven, Jannet A. Cuypers, Judith A. A. E. Boersma, Eric van den Bosch, Annemien E. Roos‐Hesselink, Jolien W. J Am Heart Assoc Original Research BACKGROUND: Adults with a systemic right ventricle (sRV) have a high risk of cardiac complications. This study aimed to identify prognostic markers in adults with sRV based on clinical evaluation, echocardiography, and blood biomarkers. METHODS AND RESULTS: In this prospective cohort study, consecutive clinically stable adults with sRV caused by Mustard‐ or congenitally corrected transposition of the great arteries were included (2011–2013). Eighty‐six patients were included (age 37±9 years, 65% male, 83% New York Heart Association functional class I, 76% Mustard transposition of the great arteries, 24% congenitally corrected transposition of the great arteries). Venous blood sampling was performed including N‐terminal pro B‐type natriuretic peptide, high‐sensitive‐troponin‐T, high‐sensitivity C‐reactive protein, growth differentiation factor‐15, galectin‐3, red cell distribution width, estimated glomerular filtration rate, and hemoglobin. Besides conventional echocardiographic measurements, longitudinal, circumferential, and radial strain were assessed using strain analysis. During a median follow‐up of 5.9 (interquartile range 5.3–6.3) years, 19 (22%) patients died or had heart failure (primary end point) and 29 (34%) patients died or had arrhythmia (secondary end point). Univariable Cox regression analysis was performed using dichotomous or standardized continuous variables. New York Heart Association functional class >I, systolic blood pressure, and most blood biomarkers were associated with the primary and secondary end point (galectin‐3 not for primary, N‐terminal pro B‐type natriuretic peptide and high‐sensitivity C‐reactive protein not for secondary end point). Growth differentiation factor‐15 showed the strongest association with both end points (hazard ratios; 2.44 [95% CI 1.67–3.57, P<0.001], 2.00 [95% CI 1.46–2.73, P<0.001], respectively). End‐diastolic basal dimension of the subpulmonary ventricle was associated with both end points (hazard ratio: 1.95 [95% CI 1.34–2.85], P<0.001, 1.70 [95% CI 1.21–2.38, P=0.002], respectively). Concerning strain analysis, only sRV septal strain was associated with the secondary end point (hazard ratio 0.58 [95% CI 0.39–0.86], P=0.006). CONCLUSIONS: Clinical, conventional echocardiographic, and blood measurements are important markers for risk stratification in adults with a sRV. The value of novel echocardiographic strain analysis seems limited. John Wiley and Sons Inc. 2019-08-21 /pmc/articles/PMC6755830/ /pubmed/31431113 http://dx.doi.org/10.1161/JAHA.119.013745 Text en © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. 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
Geenen, Laurie W.
van Grootel, Roderick W. J.
Akman, Korhan
Baggen, Vivan J. M.
Menting, Myrthe E.
Eindhoven, Jannet A.
Cuypers, Judith A. A. E.
Boersma, Eric
van den Bosch, Annemien E.
Roos‐Hesselink, Jolien W.
Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title_full Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title_fullStr Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title_full_unstemmed Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title_short Exploring the Prognostic Value of Novel Markers in Adults With a Systemic Right Ventricle
title_sort exploring the prognostic value of novel markers in adults with a systemic right ventricle
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755830/
https://www.ncbi.nlm.nih.gov/pubmed/31431113
http://dx.doi.org/10.1161/JAHA.119.013745
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