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Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study
BACKGROUND: Proenkephalin (PENK), a stable endogenous opioid biomarker related to renal function, has prognostic utility in acute and chronic heart failure. We investigated the prognostic utility of PENK in heart failure with preserved ejection fraction (HFpEF), and its relationship to renal functio...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6652170/ https://www.ncbi.nlm.nih.gov/pubmed/30767059 http://dx.doi.org/10.1007/s00392-019-01424-y |
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author | Kanagala, Prathap Squire, Iain B. Jones, Donald J. L. Cao, Thong Huy Chan, Daniel C. S. McCann, Gerry Sandhu, Jatinderpal K. Quinn, Paulene A. McAdam, John Marsh, Anna-Marie Davies, Joan E. Struck, Joachim Bergmann, Andreas Sabti, Zaid Twerenbold, Raphael Herrmann, Thomas Kozhuharov, Nikola Mueller, Christian Ng, Leong L. |
author_facet | Kanagala, Prathap Squire, Iain B. Jones, Donald J. L. Cao, Thong Huy Chan, Daniel C. S. McCann, Gerry Sandhu, Jatinderpal K. Quinn, Paulene A. McAdam, John Marsh, Anna-Marie Davies, Joan E. Struck, Joachim Bergmann, Andreas Sabti, Zaid Twerenbold, Raphael Herrmann, Thomas Kozhuharov, Nikola Mueller, Christian Ng, Leong L. |
author_sort | Kanagala, Prathap |
collection | PubMed |
description | BACKGROUND: Proenkephalin (PENK), a stable endogenous opioid biomarker related to renal function, has prognostic utility in acute and chronic heart failure. We investigated the prognostic utility of PENK in heart failure with preserved ejection fraction (HFpEF), and its relationship to renal function, Body Mass Index (BMI), and imaging measures of diastolic dysfunction. METHODS: In this multicentre study, PENK was measured in 522 HFpEF patients (ejection fraction > 50%, 253 male, mean age 76.13 ± 10.73 years) and compared to 47 age and sex-matched controls. The primary endpoint was 2-years composite of all-cause mortality and/or heart failure rehospitalisation (HF). A subset (n = 163) received detailed imaging studies. RESULTS: PENK levels were raised in HFpEF (median [interquartile range] 88.9 [62.1–132.0]) compared to normal controls (56.3 [47.9–70.5]). PENK was correlated to urea, eGFR, Body Mass Index and E/e′ (r(s) 0.635, − 0.741, − 0.275, 0.476, respectively, p < 0.0005). During 2 years follow-up 144 patients died and 220 had death/HF endpoints. Multivariable Cox regression models showed PENK independently predicted 2 year death/HF [hazard ratio (for 1 SD increment of log-transformed biomarker) HR 1.45 [95% CI 1.12–1.88, p = 0.005]], even after adjustment for troponin (HR 1.59 [1.14–2.20, p = 0.006]), and Body Mass Index (HR 1.63 [1.13–2.33, p = 0.009]). PENK showed no interaction with ejection fraction status for prediction of poor outcomes. Net reclassification analyses showed PENK significantly improved classification of death/HF outcomes for multivariable models containing natriuretic peptide, troponin and Body Mass Index (p < 0.05 for all). CONCLUSIONS: In HFpEF, PENK levels are related to BMI, and measures of diastolic dysfunction and are prognostic for all-cause mortality and heart failure rehospitalisation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00392-019-01424-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6652170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-66521702019-08-09 Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study Kanagala, Prathap Squire, Iain B. Jones, Donald J. L. Cao, Thong Huy Chan, Daniel C. S. McCann, Gerry Sandhu, Jatinderpal K. Quinn, Paulene A. McAdam, John Marsh, Anna-Marie Davies, Joan E. Struck, Joachim Bergmann, Andreas Sabti, Zaid Twerenbold, Raphael Herrmann, Thomas Kozhuharov, Nikola Mueller, Christian Ng, Leong L. Clin Res Cardiol Original Paper BACKGROUND: Proenkephalin (PENK), a stable endogenous opioid biomarker related to renal function, has prognostic utility in acute and chronic heart failure. We investigated the prognostic utility of PENK in heart failure with preserved ejection fraction (HFpEF), and its relationship to renal function, Body Mass Index (BMI), and imaging measures of diastolic dysfunction. METHODS: In this multicentre study, PENK was measured in 522 HFpEF patients (ejection fraction > 50%, 253 male, mean age 76.13 ± 10.73 years) and compared to 47 age and sex-matched controls. The primary endpoint was 2-years composite of all-cause mortality and/or heart failure rehospitalisation (HF). A subset (n = 163) received detailed imaging studies. RESULTS: PENK levels were raised in HFpEF (median [interquartile range] 88.9 [62.1–132.0]) compared to normal controls (56.3 [47.9–70.5]). PENK was correlated to urea, eGFR, Body Mass Index and E/e′ (r(s) 0.635, − 0.741, − 0.275, 0.476, respectively, p < 0.0005). During 2 years follow-up 144 patients died and 220 had death/HF endpoints. Multivariable Cox regression models showed PENK independently predicted 2 year death/HF [hazard ratio (for 1 SD increment of log-transformed biomarker) HR 1.45 [95% CI 1.12–1.88, p = 0.005]], even after adjustment for troponin (HR 1.59 [1.14–2.20, p = 0.006]), and Body Mass Index (HR 1.63 [1.13–2.33, p = 0.009]). PENK showed no interaction with ejection fraction status for prediction of poor outcomes. Net reclassification analyses showed PENK significantly improved classification of death/HF outcomes for multivariable models containing natriuretic peptide, troponin and Body Mass Index (p < 0.05 for all). CONCLUSIONS: In HFpEF, PENK levels are related to BMI, and measures of diastolic dysfunction and are prognostic for all-cause mortality and heart failure rehospitalisation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00392-019-01424-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-02-14 2019 /pmc/articles/PMC6652170/ /pubmed/30767059 http://dx.doi.org/10.1007/s00392-019-01424-y Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Paper Kanagala, Prathap Squire, Iain B. Jones, Donald J. L. Cao, Thong Huy Chan, Daniel C. S. McCann, Gerry Sandhu, Jatinderpal K. Quinn, Paulene A. McAdam, John Marsh, Anna-Marie Davies, Joan E. Struck, Joachim Bergmann, Andreas Sabti, Zaid Twerenbold, Raphael Herrmann, Thomas Kozhuharov, Nikola Mueller, Christian Ng, Leong L. Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title | Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title_full | Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title_fullStr | Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title_full_unstemmed | Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title_short | Proenkephalin and prognosis in heart failure with preserved ejection fraction: a GREAT network study |
title_sort | proenkephalin and prognosis in heart failure with preserved ejection fraction: a great network study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6652170/ https://www.ncbi.nlm.nih.gov/pubmed/30767059 http://dx.doi.org/10.1007/s00392-019-01424-y |
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