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The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction
BACKGROUND: Recurrent cardiovascular events following acute myocardial infarction (AMI) are common. The purpose of this study was to evaluate the impact of platelet aggregation, PFA-100 closure times and peak C-reactive protein (CRP), respectively, on the occurrence of death, myocardial infarction a...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715384/ https://www.ncbi.nlm.nih.gov/pubmed/19583836 http://dx.doi.org/10.1186/1477-9560-7-12 |
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author | Modica, Angelo Karlsson, Fredrik Mooe, Thomas |
author_facet | Modica, Angelo Karlsson, Fredrik Mooe, Thomas |
author_sort | Modica, Angelo |
collection | PubMed |
description | BACKGROUND: Recurrent cardiovascular events following acute myocardial infarction (AMI) are common. The purpose of this study was to evaluate the impact of platelet aggregation, PFA-100 closure times and peak C-reactive protein (CRP), respectively, on the occurrence of death, myocardial infarction and ischemic cerebral events after an AMI. Furthermore, to examine the relationship between the platelet function tests and peak CRP. METHODS: Three hundred and thirty-four patients with AMI were included in the study. Platelet aggregation was analyzed by an aggregometer using laser light (PA-200). The state of high residual platelet reactivity was defined as normal closure times (PFA-100) during treatment with aspirin. RESULTS: The fourth quartile of peak CRP was associated with poorer outcome as compared to the first quartile in a multivariate Cox-regression analysis, with a hazard ratio of 2.0 (95% CI 1.1–3.7) for the occurrence of death, myocardial infarction and ischemic cerebral events. The fourth quartile of peak CRP (>64.6 mg/l) was associated with platelet aggregation (p < 0.001, adjusted R(2 )= 0.13) and high residual platelet reactivity, in a multivariate model, with an odds ratio of 2.9 (CI 95% 1.3–6.8), as compared to the first quartile. Neither the highest quartile of platelet aggregation nor the state of high residual platelet reactivity predicted new cardiovascular events. CONCLUSION: In patients with myocardial infarction, measured peak CRP is associated with new cardiovascular events. Despite an association with peak CRP neither more pronounced platelet aggregation nor PFA-100 closure times independently predict new cardiovascular events. |
format | Text |
id | pubmed-2715384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27153842009-07-25 The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction Modica, Angelo Karlsson, Fredrik Mooe, Thomas Thromb J Original Clinical Investigation BACKGROUND: Recurrent cardiovascular events following acute myocardial infarction (AMI) are common. The purpose of this study was to evaluate the impact of platelet aggregation, PFA-100 closure times and peak C-reactive protein (CRP), respectively, on the occurrence of death, myocardial infarction and ischemic cerebral events after an AMI. Furthermore, to examine the relationship between the platelet function tests and peak CRP. METHODS: Three hundred and thirty-four patients with AMI were included in the study. Platelet aggregation was analyzed by an aggregometer using laser light (PA-200). The state of high residual platelet reactivity was defined as normal closure times (PFA-100) during treatment with aspirin. RESULTS: The fourth quartile of peak CRP was associated with poorer outcome as compared to the first quartile in a multivariate Cox-regression analysis, with a hazard ratio of 2.0 (95% CI 1.1–3.7) for the occurrence of death, myocardial infarction and ischemic cerebral events. The fourth quartile of peak CRP (>64.6 mg/l) was associated with platelet aggregation (p < 0.001, adjusted R(2 )= 0.13) and high residual platelet reactivity, in a multivariate model, with an odds ratio of 2.9 (CI 95% 1.3–6.8), as compared to the first quartile. Neither the highest quartile of platelet aggregation nor the state of high residual platelet reactivity predicted new cardiovascular events. CONCLUSION: In patients with myocardial infarction, measured peak CRP is associated with new cardiovascular events. Despite an association with peak CRP neither more pronounced platelet aggregation nor PFA-100 closure times independently predict new cardiovascular events. BioMed Central 2009-07-07 /pmc/articles/PMC2715384/ /pubmed/19583836 http://dx.doi.org/10.1186/1477-9560-7-12 Text en Copyright © 2009 Modica et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Clinical Investigation Modica, Angelo Karlsson, Fredrik Mooe, Thomas The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title | The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title_full | The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title_fullStr | The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title_full_unstemmed | The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title_short | The impact of platelet function or C-reactive protein, on cardiovascular events after an acute myocardial infarction |
title_sort | impact of platelet function or c-reactive protein, on cardiovascular events after an acute myocardial infarction |
topic | Original Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715384/ https://www.ncbi.nlm.nih.gov/pubmed/19583836 http://dx.doi.org/10.1186/1477-9560-7-12 |
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