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Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction
OBJECTIVE: To assess the usefulness of in-hospital measurement of C-reactive protein (CRP) concentration in comparison to well-established risk factors as a marker of post-infarct left ventricular systolic dysfunction (LVSD) at discharge. MATERIALS AND METHODS: Two hundred and four consecutive patie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SP Birkhäuser Verlag Basel
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375005/ https://www.ncbi.nlm.nih.gov/pubmed/22446726 http://dx.doi.org/10.1007/s00011-012-0466-2 |
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author | Swiatkiewicz, Iwona Kozinski, Marek Magielski, Przemyslaw Gierach, Joanna Fabiszak, Tomasz Kubica, Aldona Sukiennik, Adam Navarese, Eliano Pio Odrowaz-Sypniewska, Grazyna Kubica, Jacek |
author_facet | Swiatkiewicz, Iwona Kozinski, Marek Magielski, Przemyslaw Gierach, Joanna Fabiszak, Tomasz Kubica, Aldona Sukiennik, Adam Navarese, Eliano Pio Odrowaz-Sypniewska, Grazyna Kubica, Jacek |
author_sort | Swiatkiewicz, Iwona |
collection | PubMed |
description | OBJECTIVE: To assess the usefulness of in-hospital measurement of C-reactive protein (CRP) concentration in comparison to well-established risk factors as a marker of post-infarct left ventricular systolic dysfunction (LVSD) at discharge. MATERIALS AND METHODS: Two hundred and four consecutive patients with ST-segment-elevation myocardial infarction (STEMI) were prospectively enrolled into the study. CRP plasma concentrations were measured before reperfusion, 24 h after admission and at discharge with an ultra-sensitive latex immunoassay. RESULTS: CRP concentration increased significantly during the first 24 h of hospitalization (2.4 ± 1.9 vs. 15.7 ± 17.0 mg/L; p < 0.001) and persisted elevated at discharge (14.7 ± 14.7 mg/L), mainly in 57 patients with LVSD (2.4 ± 1.8 vs. 25.0 ± 23.4 mg/L; p < 0.001; CRP at discharge 21.9 ± 18.6 mg/L). The prevalence of LVSD was significantly increased across increasing tertiles of CRP concentration both at 24 h after admission (13.2 vs. 19.1 vs. 51.5 %; p < 0.0001) and at discharge (14.7 vs. 23.5 vs. 45.6 %; p < 0.0001). Multivariate analysis demonstrated CRP concentration at discharge to be an independent marker of early LVSD (odds ratio of 1.38 for a 10 mg/L increase, 95 % confidence interval 1.01–1.87; p < 0.04). CONCLUSION: Measurement of CRP plasma concentration at discharge may be useful as a marker of early LVSD in patients after a first STEMI. |
format | Online Article Text |
id | pubmed-3375005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | SP Birkhäuser Verlag Basel |
record_format | MEDLINE/PubMed |
spelling | pubmed-33750052012-06-18 Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction Swiatkiewicz, Iwona Kozinski, Marek Magielski, Przemyslaw Gierach, Joanna Fabiszak, Tomasz Kubica, Aldona Sukiennik, Adam Navarese, Eliano Pio Odrowaz-Sypniewska, Grazyna Kubica, Jacek Inflamm Res Original Research Paper OBJECTIVE: To assess the usefulness of in-hospital measurement of C-reactive protein (CRP) concentration in comparison to well-established risk factors as a marker of post-infarct left ventricular systolic dysfunction (LVSD) at discharge. MATERIALS AND METHODS: Two hundred and four consecutive patients with ST-segment-elevation myocardial infarction (STEMI) were prospectively enrolled into the study. CRP plasma concentrations were measured before reperfusion, 24 h after admission and at discharge with an ultra-sensitive latex immunoassay. RESULTS: CRP concentration increased significantly during the first 24 h of hospitalization (2.4 ± 1.9 vs. 15.7 ± 17.0 mg/L; p < 0.001) and persisted elevated at discharge (14.7 ± 14.7 mg/L), mainly in 57 patients with LVSD (2.4 ± 1.8 vs. 25.0 ± 23.4 mg/L; p < 0.001; CRP at discharge 21.9 ± 18.6 mg/L). The prevalence of LVSD was significantly increased across increasing tertiles of CRP concentration both at 24 h after admission (13.2 vs. 19.1 vs. 51.5 %; p < 0.0001) and at discharge (14.7 vs. 23.5 vs. 45.6 %; p < 0.0001). Multivariate analysis demonstrated CRP concentration at discharge to be an independent marker of early LVSD (odds ratio of 1.38 for a 10 mg/L increase, 95 % confidence interval 1.01–1.87; p < 0.04). CONCLUSION: Measurement of CRP plasma concentration at discharge may be useful as a marker of early LVSD in patients after a first STEMI. SP Birkhäuser Verlag Basel 2012-03-24 2012 /pmc/articles/PMC3375005/ /pubmed/22446726 http://dx.doi.org/10.1007/s00011-012-0466-2 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Research Paper Swiatkiewicz, Iwona Kozinski, Marek Magielski, Przemyslaw Gierach, Joanna Fabiszak, Tomasz Kubica, Aldona Sukiennik, Adam Navarese, Eliano Pio Odrowaz-Sypniewska, Grazyna Kubica, Jacek Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title | Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title_full | Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title_fullStr | Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title_full_unstemmed | Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title_short | Usefulness of C-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
title_sort | usefulness of c-reactive protein as a marker of early post-infarct left ventricular systolic dysfunction |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3375005/ https://www.ncbi.nlm.nih.gov/pubmed/22446726 http://dx.doi.org/10.1007/s00011-012-0466-2 |
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