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Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients
AIMS: Evidence on the association of macrophage‐ and neutrophil‐related blood biomarkers with clinical outcome in heart failure patients is limited, and, with the exception of C‐reactive protein, no data exist on their temporal evolution. We aimed to investigate whether temporal patterns of these bi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261550/ https://www.ncbi.nlm.nih.gov/pubmed/32196993 http://dx.doi.org/10.1002/ehf2.12678 |
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author | Klimczak‐Tomaniak, Dominika Bouwens, Elke Schuurman, Anne‐Sophie Akkerhuis, K. Martijn Constantinescu, Alina Brugts, Jasper Westenbrink, B. Daan van Ramshorst, Jan Germans, Tjeerd Pączek, Leszek Umans, Victor Boersma, Eric Kardys, Isabella |
author_facet | Klimczak‐Tomaniak, Dominika Bouwens, Elke Schuurman, Anne‐Sophie Akkerhuis, K. Martijn Constantinescu, Alina Brugts, Jasper Westenbrink, B. Daan van Ramshorst, Jan Germans, Tjeerd Pączek, Leszek Umans, Victor Boersma, Eric Kardys, Isabella |
author_sort | Klimczak‐Tomaniak, Dominika |
collection | PubMed |
description | AIMS: Evidence on the association of macrophage‐ and neutrophil‐related blood biomarkers with clinical outcome in heart failure patients is limited, and, with the exception of C‐reactive protein, no data exist on their temporal evolution. We aimed to investigate whether temporal patterns of these biomarkers are related to clinical outcome in patients with stable chronic heart failure (CHF). METHODS AND RESULTS: In 263 patients with CHF, we performed serial plasma measurements of scavenger receptor cysteine‐rich type 1 protein M130 (CD163), tartrate‐resistant acid phosphatase type 5 (TRAP), granulins (GRN), spondin‐1 (SPON1), peptidoglycan recognition protein 1 (PGLYRP1), and tissue factor pathway inhibitor (TFPI). The Cardiovascular Panel III (Olink Proteomics AB, Uppsala, Sweden) was used. During 2.2 years of follow‐up, we collected 1984 samples before the occurrence of the composite primary endpoint (PE) or censoring. For efficiency, we selected 567 samples for the measurements (all baseline samples, the last two samples preceding the PE, and the last sample before censoring in event‐free patients). The relationship between repeatedly measured biomarker levels and the PE was evaluated by joint models. Mean (±standard deviation) age was 67 ± 13 years; 189 (72%) were men; left ventricular ejection fraction (%) was 32 ± 11. During follow‐up, 70 (27%) patients experienced the PE. Serially measured biomarkers predicted the PE in a multivariable model adjusted for baseline clinical characteristics [hazard ratio (95% confidence interval) per 1‐standard deviation change in biomarker]: CD163 [2.07(1.47–2.98), P < 0.001], TRAP [0.62 (0.43–0.90), P = 0.009], GRN [2.46 (1.64–3.84), P < 0.001], SPON1 [3.94 (2.50–6.50), P < 0.001], and PGLYRP1 [1.62 (1.14–2.31), P = 0.006]. CONCLUSIONS: Changes in plasma levels of CD163, TRAP, GRN, SPON1, and PGLYRP1 precede adverse cardiovascular events in patients with CHF. |
format | Online Article Text |
id | pubmed-7261550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72615502020-06-01 Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients Klimczak‐Tomaniak, Dominika Bouwens, Elke Schuurman, Anne‐Sophie Akkerhuis, K. Martijn Constantinescu, Alina Brugts, Jasper Westenbrink, B. Daan van Ramshorst, Jan Germans, Tjeerd Pączek, Leszek Umans, Victor Boersma, Eric Kardys, Isabella ESC Heart Fail Original Research Articles AIMS: Evidence on the association of macrophage‐ and neutrophil‐related blood biomarkers with clinical outcome in heart failure patients is limited, and, with the exception of C‐reactive protein, no data exist on their temporal evolution. We aimed to investigate whether temporal patterns of these biomarkers are related to clinical outcome in patients with stable chronic heart failure (CHF). METHODS AND RESULTS: In 263 patients with CHF, we performed serial plasma measurements of scavenger receptor cysteine‐rich type 1 protein M130 (CD163), tartrate‐resistant acid phosphatase type 5 (TRAP), granulins (GRN), spondin‐1 (SPON1), peptidoglycan recognition protein 1 (PGLYRP1), and tissue factor pathway inhibitor (TFPI). The Cardiovascular Panel III (Olink Proteomics AB, Uppsala, Sweden) was used. During 2.2 years of follow‐up, we collected 1984 samples before the occurrence of the composite primary endpoint (PE) or censoring. For efficiency, we selected 567 samples for the measurements (all baseline samples, the last two samples preceding the PE, and the last sample before censoring in event‐free patients). The relationship between repeatedly measured biomarker levels and the PE was evaluated by joint models. Mean (±standard deviation) age was 67 ± 13 years; 189 (72%) were men; left ventricular ejection fraction (%) was 32 ± 11. During follow‐up, 70 (27%) patients experienced the PE. Serially measured biomarkers predicted the PE in a multivariable model adjusted for baseline clinical characteristics [hazard ratio (95% confidence interval) per 1‐standard deviation change in biomarker]: CD163 [2.07(1.47–2.98), P < 0.001], TRAP [0.62 (0.43–0.90), P = 0.009], GRN [2.46 (1.64–3.84), P < 0.001], SPON1 [3.94 (2.50–6.50), P < 0.001], and PGLYRP1 [1.62 (1.14–2.31), P = 0.006]. CONCLUSIONS: Changes in plasma levels of CD163, TRAP, GRN, SPON1, and PGLYRP1 precede adverse cardiovascular events in patients with CHF. John Wiley and Sons Inc. 2020-03-20 /pmc/articles/PMC7261550/ /pubmed/32196993 http://dx.doi.org/10.1002/ehf2.12678 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology 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 Articles Klimczak‐Tomaniak, Dominika Bouwens, Elke Schuurman, Anne‐Sophie Akkerhuis, K. Martijn Constantinescu, Alina Brugts, Jasper Westenbrink, B. Daan van Ramshorst, Jan Germans, Tjeerd Pączek, Leszek Umans, Victor Boersma, Eric Kardys, Isabella Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title | Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title_full | Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title_fullStr | Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title_full_unstemmed | Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title_short | Temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
title_sort | temporal patterns of macrophage‐ and neutrophil‐related markers are associated with clinical outcome in heart failure patients |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261550/ https://www.ncbi.nlm.nih.gov/pubmed/32196993 http://dx.doi.org/10.1002/ehf2.12678 |
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