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The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction
AIMS: Heart failure with normal ejection fraction (HFnEF) is an important clinical entity that remains incompletely understood. The novel biomarker growth differentiation factor 15 (GDF-15) is elevated in systolic heart failure (HFrEF) and is predictive of an adverse outcome. We investigated the cli...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990410/ https://www.ncbi.nlm.nih.gov/pubmed/20837635 http://dx.doi.org/10.1093/eurjhf/hfq151 |
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author | Stahrenberg, Raoul Edelmann, Frank Mende, Meinhard Kockskämper, Anke Düngen, Hans-Dirk Lüers, Claus Binder, Lutz Herrmann-Lingen, Christoph Gelbrich, Götz Hasenfuß, Gerd Pieske, Burkert Wachter, Rolf |
author_facet | Stahrenberg, Raoul Edelmann, Frank Mende, Meinhard Kockskämper, Anke Düngen, Hans-Dirk Lüers, Claus Binder, Lutz Herrmann-Lingen, Christoph Gelbrich, Götz Hasenfuß, Gerd Pieske, Burkert Wachter, Rolf |
author_sort | Stahrenberg, Raoul |
collection | PubMed |
description | AIMS: Heart failure with normal ejection fraction (HFnEF) is an important clinical entity that remains incompletely understood. The novel biomarker growth differentiation factor 15 (GDF-15) is elevated in systolic heart failure (HFrEF) and is predictive of an adverse outcome. We investigated the clinical relevance of GDF-15 plasma levels in HFnEF. METHODS AND RESULTS: A subgroup of patients from the ongoing DIAST-CHF observational trial, with a history of chronic heart failure (CHF) or positive Framingham criteria at presentation, was selected. Patients were classified as having either HFrEF (n = 86) or HFnEF (n = 142) and compared with healthy elderly controls (n = 188) from the same cohort. Growth differentiation factor 15 levels in HFnEF were significantly higher than in controls and similar to those in HFrEF. In multivariate analysis, factors significantly associated with GDF-15 levels were age, sex, estimated glomerular filtration rate (eGFR), presence of HFrEF and HFnEF. Growth differentiation factor 15 correlated with multiple echocardiographic markers of diastolic function and was associated with 6 min walk test performance and SF-36 physical score on multivariate analysis in all patients. When using a classification for HFnEF that did not employ N-terminal pro brain natriuretic peptide (NT-proBNP) as a diagnostic criterion, the diagnostic properties of GDF-15 for detecting HFnEF tended to be superior to those of NT-proBNP, and a combination significantly improved diagnostic accuracy. CONCLUSION: Growth differentiation factor 15 is elevated in HFnEF to a similar degree as in HFrEF. It is independently associated with impairment in exercise capacity and in physical components of quality of life. Diagnostic precision of GDF-15 is at least as good as that of NT-proBNP and combining both markers improves diagnostic accuracy. |
format | Text |
id | pubmed-2990410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-29904102010-11-24 The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction Stahrenberg, Raoul Edelmann, Frank Mende, Meinhard Kockskämper, Anke Düngen, Hans-Dirk Lüers, Claus Binder, Lutz Herrmann-Lingen, Christoph Gelbrich, Götz Hasenfuß, Gerd Pieske, Burkert Wachter, Rolf Eur J Heart Fail Biomarkers AIMS: Heart failure with normal ejection fraction (HFnEF) is an important clinical entity that remains incompletely understood. The novel biomarker growth differentiation factor 15 (GDF-15) is elevated in systolic heart failure (HFrEF) and is predictive of an adverse outcome. We investigated the clinical relevance of GDF-15 plasma levels in HFnEF. METHODS AND RESULTS: A subgroup of patients from the ongoing DIAST-CHF observational trial, with a history of chronic heart failure (CHF) or positive Framingham criteria at presentation, was selected. Patients were classified as having either HFrEF (n = 86) or HFnEF (n = 142) and compared with healthy elderly controls (n = 188) from the same cohort. Growth differentiation factor 15 levels in HFnEF were significantly higher than in controls and similar to those in HFrEF. In multivariate analysis, factors significantly associated with GDF-15 levels were age, sex, estimated glomerular filtration rate (eGFR), presence of HFrEF and HFnEF. Growth differentiation factor 15 correlated with multiple echocardiographic markers of diastolic function and was associated with 6 min walk test performance and SF-36 physical score on multivariate analysis in all patients. When using a classification for HFnEF that did not employ N-terminal pro brain natriuretic peptide (NT-proBNP) as a diagnostic criterion, the diagnostic properties of GDF-15 for detecting HFnEF tended to be superior to those of NT-proBNP, and a combination significantly improved diagnostic accuracy. CONCLUSION: Growth differentiation factor 15 is elevated in HFnEF to a similar degree as in HFrEF. It is independently associated with impairment in exercise capacity and in physical components of quality of life. Diagnostic precision of GDF-15 is at least as good as that of NT-proBNP and combining both markers improves diagnostic accuracy. Oxford University Press 2010-12 2010-09-13 /pmc/articles/PMC2990410/ /pubmed/20837635 http://dx.doi.org/10.1093/eurjhf/hfq151 Text en Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2010. For permissions please email: journals.permissions@oxfordjournals.org. http://creativecommons.org/licenses/by-nc/2.5/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that the original authorship is properly and fully attributed; the Journal, Learned Society and Oxford University Press are attributed as the original place of publication with correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Biomarkers Stahrenberg, Raoul Edelmann, Frank Mende, Meinhard Kockskämper, Anke Düngen, Hans-Dirk Lüers, Claus Binder, Lutz Herrmann-Lingen, Christoph Gelbrich, Götz Hasenfuß, Gerd Pieske, Burkert Wachter, Rolf The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title | The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title_full | The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title_fullStr | The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title_full_unstemmed | The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title_short | The novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
title_sort | novel biomarker growth differentiation factor 15 in heart failure with normal ejection fraction |
topic | Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2990410/ https://www.ncbi.nlm.nih.gov/pubmed/20837635 http://dx.doi.org/10.1093/eurjhf/hfq151 |
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