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Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction
Pentraxin-3 (PTX3) and neprilysin have been associated with increased morbidity and mortality in chronic inflammatory disease and heart failure, but these biomarkers have been studied less in patients with ST segment elevation myocardial infarction (STEMI). We investigated the dynamic changes in the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869300/ https://www.ncbi.nlm.nih.gov/pubmed/35203485 http://dx.doi.org/10.3390/biomedicines10020275 |
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author | Befekadu, Rahel Grenegård, Magnus Larsson, Anders Christensen, Kjeld Ramström, Sofia |
author_facet | Befekadu, Rahel Grenegård, Magnus Larsson, Anders Christensen, Kjeld Ramström, Sofia |
author_sort | Befekadu, Rahel |
collection | PubMed |
description | Pentraxin-3 (PTX3) and neprilysin have been associated with increased morbidity and mortality in chronic inflammatory disease and heart failure, but these biomarkers have been studied less in patients with ST segment elevation myocardial infarction (STEMI). We investigated the dynamic changes in these biomarkers, as well as the well-known C-reactive protein (CRP), in STEMI patients. PTX3, neprilysin and CRP were measured in samples from 165 STEMI patients, collected at the acute stage, 1–3 days after and 3 months after percutaneous coronary intervention (PCI), and from 40 healthy donors. Patient survival was followed for approximately 8 years after the PCI. As compared with samples from healthy donors, plasma levels of CRP and PTX3 were significantly increased in the acute samples and 1–3 days after PCI, but not at 3 months. CRP levels peaked at 1–3 days, while PTX3 was similarly high in both acute and 1–3 days samples. For neprilysin, no significant differences were observed at the group level. We found no significant differences when comparing patients with patent versus occluded culprit vessels or between patients having a thrombus aspiration or not. However, we found a significant reduction in survival for individuals with PTX3 above the median, both for samples collected at the acute stage and 1–3 days after PCI (p = 0.0001 and p = 0.0008, respectively). For CRP, no significant differences were observed using this approach, but patients above the reference range for healthy donors in the acute samples showed significantly lower survival (p = 0.0476). Conclusions: Survival analysis suggests that PTX3 might be a promising marker to predict mortality in this patient population. |
format | Online Article Text |
id | pubmed-8869300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88693002022-02-25 Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction Befekadu, Rahel Grenegård, Magnus Larsson, Anders Christensen, Kjeld Ramström, Sofia Biomedicines Article Pentraxin-3 (PTX3) and neprilysin have been associated with increased morbidity and mortality in chronic inflammatory disease and heart failure, but these biomarkers have been studied less in patients with ST segment elevation myocardial infarction (STEMI). We investigated the dynamic changes in these biomarkers, as well as the well-known C-reactive protein (CRP), in STEMI patients. PTX3, neprilysin and CRP were measured in samples from 165 STEMI patients, collected at the acute stage, 1–3 days after and 3 months after percutaneous coronary intervention (PCI), and from 40 healthy donors. Patient survival was followed for approximately 8 years after the PCI. As compared with samples from healthy donors, plasma levels of CRP and PTX3 were significantly increased in the acute samples and 1–3 days after PCI, but not at 3 months. CRP levels peaked at 1–3 days, while PTX3 was similarly high in both acute and 1–3 days samples. For neprilysin, no significant differences were observed at the group level. We found no significant differences when comparing patients with patent versus occluded culprit vessels or between patients having a thrombus aspiration or not. However, we found a significant reduction in survival for individuals with PTX3 above the median, both for samples collected at the acute stage and 1–3 days after PCI (p = 0.0001 and p = 0.0008, respectively). For CRP, no significant differences were observed using this approach, but patients above the reference range for healthy donors in the acute samples showed significantly lower survival (p = 0.0476). Conclusions: Survival analysis suggests that PTX3 might be a promising marker to predict mortality in this patient population. MDPI 2022-01-26 /pmc/articles/PMC8869300/ /pubmed/35203485 http://dx.doi.org/10.3390/biomedicines10020275 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Befekadu, Rahel Grenegård, Magnus Larsson, Anders Christensen, Kjeld Ramström, Sofia Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title | Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title_full | Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title_fullStr | Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title_full_unstemmed | Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title_short | Dynamic Changes in Pentraxin-3 and Neprilysin in ST Segment Elevation Myocardial Infarction |
title_sort | dynamic changes in pentraxin-3 and neprilysin in st segment elevation myocardial infarction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869300/ https://www.ncbi.nlm.nih.gov/pubmed/35203485 http://dx.doi.org/10.3390/biomedicines10020275 |
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