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Serial Analyses of C‐Reactive Protein and Myeloperoxidase in Acute Coronary Syndrome

Background C‐reactive protein (CRP) and myeloperoxidase (MPO) are involved in the pathogenesis of atherosclerosis, mainly during periods of instabilization. This study aims to test the hypothesis that patients with acute coronary syndrome (ACS) maintain a persistent inflammatory state, and that this...

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Published in:Clinical cardiology (Mahwah, N.J.) N.J.), 2009-11, Vol.32 (11), p.E58-E62
Main Authors: Borges, Flávia K., Borges, Fernando K., Stella, Steffan F., Souza, Juliana F., Wendland, Andréa E., Werres Junior, Luis Carlos, Ribeiro, Jorge P., Polanczyk, Carísi A.
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container_title Clinical cardiology (Mahwah, N.J.)
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creator Borges, Flávia K.
Borges, Fernando K.
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Werres Junior, Luis Carlos
Ribeiro, Jorge P.
Polanczyk, Carísi A.
description Background C‐reactive protein (CRP) and myeloperoxidase (MPO) are involved in the pathogenesis of atherosclerosis, mainly during periods of instabilization. This study aims to test the hypothesis that patients with acute coronary syndrome (ACS) maintain a persistent inflammatory state, and that this is associated with long‐term mortality. Hypothesis We hypothesized that serum C‐reactive protein and myeloperoxidase collected at the index event and later, could add to the prognostic information in patients with ACS. Methods In a prospective cohort of 115 consecutive patients with ACS, myeloperoxidase and C‐reactive protein were measured at admission and 2 y later. Patients were followed‐up for the occurrence of cardiac death and other major cardiac events. Results Levels of CRP decreased from 26 ± 34 mg/L in the acute phase to 6 ± 8 mg/L in the chronic phase (p < 0.001), and MPO levels decreased from 86 ± 43 pM to 27 ± 32 pM (p < 0.001). After 29 ± 12 mo, 27% patients died, 39% had new episode of ACS, and 30% underwent revascularization procedures. Initial CRP levels above 10 mg/L were associated with higher long‐term mortality (hazard ratio [HR]: 2.43; 95% confidence interval [CI]: 0.98 to 6.07; p = 0.048). MPO levels were not associated with death or other major events. Conclusions Changes over time or absolute values in the chronic phase of both markers were not associated with clinical outcomes. CRP levels, but not MPO levels, in the index event were predictive of long‐term cardiovascular mortality. Copyright © 2009 Wiley Periodicals, Inc.
doi_str_mv 10.1002/clc.20462
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This study aims to test the hypothesis that patients with acute coronary syndrome (ACS) maintain a persistent inflammatory state, and that this is associated with long‐term mortality. Hypothesis We hypothesized that serum C‐reactive protein and myeloperoxidase collected at the index event and later, could add to the prognostic information in patients with ACS. Methods In a prospective cohort of 115 consecutive patients with ACS, myeloperoxidase and C‐reactive protein were measured at admission and 2 y later. Patients were followed‐up for the occurrence of cardiac death and other major cardiac events. Results Levels of CRP decreased from 26 ± 34 mg/L in the acute phase to 6 ± 8 mg/L in the chronic phase (p &lt; 0.001), and MPO levels decreased from 86 ± 43 pM to 27 ± 32 pM (p &lt; 0.001). After 29 ± 12 mo, 27% patients died, 39% had new episode of ACS, and 30% underwent revascularization procedures. Initial CRP levels above 10 mg/L were associated with higher long‐term mortality (hazard ratio [HR]: 2.43; 95% confidence interval [CI]: 0.98 to 6.07; p = 0.048). MPO levels were not associated with death or other major events. Conclusions Changes over time or absolute values in the chronic phase of both markers were not associated with clinical outcomes. CRP levels, but not MPO levels, in the index event were predictive of long‐term cardiovascular mortality. Copyright © 2009 Wiley Periodicals, Inc.</description><identifier>ISSN: 0160-9289</identifier><identifier>ISSN: 1932-8737</identifier><identifier>EISSN: 1932-8737</identifier><identifier>DOI: 10.1002/clc.20462</identifier><identifier>PMID: 19816870</identifier><language>eng</language><publisher>New York: Wiley Periodicals, Inc</publisher><subject>Acute Coronary Syndrome - enzymology ; Acute Coronary Syndrome - immunology ; Acute Coronary Syndrome - mortality ; Acute Coronary Syndrome - therapy ; Aged ; Biomarkers - blood ; C-Reactive Protein - metabolism ; Case Report ; Case Reports ; Female ; Humans ; inflammation ; Inflammation Mediators - blood ; Kaplan-Meier Estimate ; Male ; markers ; Middle Aged ; myocardial infarction ; Peroxidase - blood ; prognosis ; Proportional Hazards Models ; Prospective Studies ; Risk Assessment ; Risk Factors ; Time Factors ; Treatment Outcome ; unstable angina</subject><ispartof>Clinical cardiology (Mahwah, N.J.), 2009-11, Vol.32 (11), p.E58-E62</ispartof><rights>Copyright © 2009 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3292-9794ffd3ae16cf0d1336f40cb175784044352c83d70771b84db5c4e8df4ea0ca3</citedby><cites>FETCH-LOGICAL-c3292-9794ffd3ae16cf0d1336f40cb175784044352c83d70771b84db5c4e8df4ea0ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653307/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6653307/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19816870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borges, Flávia K.</creatorcontrib><creatorcontrib>Borges, Fernando K.</creatorcontrib><creatorcontrib>Stella, Steffan F.</creatorcontrib><creatorcontrib>Souza, Juliana F.</creatorcontrib><creatorcontrib>Wendland, Andréa E.</creatorcontrib><creatorcontrib>Werres Junior, Luis Carlos</creatorcontrib><creatorcontrib>Ribeiro, Jorge P.</creatorcontrib><creatorcontrib>Polanczyk, Carísi A.</creatorcontrib><title>Serial Analyses of C‐Reactive Protein and Myeloperoxidase in Acute Coronary Syndrome</title><title>Clinical cardiology (Mahwah, N.J.)</title><addtitle>Clin Cardiol</addtitle><description>Background C‐reactive protein (CRP) and myeloperoxidase (MPO) are involved in the pathogenesis of atherosclerosis, mainly during periods of instabilization. This study aims to test the hypothesis that patients with acute coronary syndrome (ACS) maintain a persistent inflammatory state, and that this is associated with long‐term mortality. Hypothesis We hypothesized that serum C‐reactive protein and myeloperoxidase collected at the index event and later, could add to the prognostic information in patients with ACS. Methods In a prospective cohort of 115 consecutive patients with ACS, myeloperoxidase and C‐reactive protein were measured at admission and 2 y later. Patients were followed‐up for the occurrence of cardiac death and other major cardiac events. Results Levels of CRP decreased from 26 ± 34 mg/L in the acute phase to 6 ± 8 mg/L in the chronic phase (p &lt; 0.001), and MPO levels decreased from 86 ± 43 pM to 27 ± 32 pM (p &lt; 0.001). After 29 ± 12 mo, 27% patients died, 39% had new episode of ACS, and 30% underwent revascularization procedures. Initial CRP levels above 10 mg/L were associated with higher long‐term mortality (hazard ratio [HR]: 2.43; 95% confidence interval [CI]: 0.98 to 6.07; p = 0.048). MPO levels were not associated with death or other major events. Conclusions Changes over time or absolute values in the chronic phase of both markers were not associated with clinical outcomes. CRP levels, but not MPO levels, in the index event were predictive of long‐term cardiovascular mortality. 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This study aims to test the hypothesis that patients with acute coronary syndrome (ACS) maintain a persistent inflammatory state, and that this is associated with long‐term mortality. Hypothesis We hypothesized that serum C‐reactive protein and myeloperoxidase collected at the index event and later, could add to the prognostic information in patients with ACS. Methods In a prospective cohort of 115 consecutive patients with ACS, myeloperoxidase and C‐reactive protein were measured at admission and 2 y later. Patients were followed‐up for the occurrence of cardiac death and other major cardiac events. Results Levels of CRP decreased from 26 ± 34 mg/L in the acute phase to 6 ± 8 mg/L in the chronic phase (p &lt; 0.001), and MPO levels decreased from 86 ± 43 pM to 27 ± 32 pM (p &lt; 0.001). After 29 ± 12 mo, 27% patients died, 39% had new episode of ACS, and 30% underwent revascularization procedures. Initial CRP levels above 10 mg/L were associated with higher long‐term mortality (hazard ratio [HR]: 2.43; 95% confidence interval [CI]: 0.98 to 6.07; p = 0.048). MPO levels were not associated with death or other major events. Conclusions Changes over time or absolute values in the chronic phase of both markers were not associated with clinical outcomes. CRP levels, but not MPO levels, in the index event were predictive of long‐term cardiovascular mortality. Copyright © 2009 Wiley Periodicals, Inc.</abstract><cop>New York</cop><pub>Wiley Periodicals, Inc</pub><pmid>19816870</pmid><doi>10.1002/clc.20462</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute Coronary Syndrome - enzymology
Acute Coronary Syndrome - immunology
Acute Coronary Syndrome - mortality
Acute Coronary Syndrome - therapy
Aged
Biomarkers - blood
C-Reactive Protein - metabolism
Case Report
Case Reports
Female
Humans
inflammation
Inflammation Mediators - blood
Kaplan-Meier Estimate
Male
markers
Middle Aged
myocardial infarction
Peroxidase - blood
prognosis
Proportional Hazards Models
Prospective Studies
Risk Assessment
Risk Factors
Time Factors
Treatment Outcome
unstable angina
title Serial Analyses of C‐Reactive Protein and Myeloperoxidase in Acute Coronary Syndrome
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