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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 |
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container_title | Clinical cardiology (Mahwah, N.J.) |
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creator | 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. |
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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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.</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 < 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.</description><subject>Acute Coronary Syndrome - enzymology</subject><subject>Acute Coronary Syndrome - immunology</subject><subject>Acute Coronary Syndrome - mortality</subject><subject>Acute Coronary Syndrome - therapy</subject><subject>Aged</subject><subject>Biomarkers - blood</subject><subject>C-Reactive Protein - metabolism</subject><subject>Case Report</subject><subject>Case Reports</subject><subject>Female</subject><subject>Humans</subject><subject>inflammation</subject><subject>Inflammation Mediators - blood</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>markers</subject><subject>Middle Aged</subject><subject>myocardial infarction</subject><subject>Peroxidase - blood</subject><subject>prognosis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>unstable angina</subject><issn>0160-9289</issn><issn>1932-8737</issn><issn>1932-8737</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp1kc1uEzEQxy0EIiFw4AWQb4jDJv7atfdSKVrxUSkViABXy7FnqStnHexNYW88As_YJ-mmiUo5cBpp5qffjOaP0EtK5pQQtrDBzhkRFXuEprTmrFCSy8doSmhFipqpeoKe5Xw1okQx_hRNaK1opSSZom9rSN4EvOxMGDJkHFvc3Pz-8xmM7f014E8p9uA7bDqHLwYIcQcp_vLOZMBje2n3PeAmptiZNOD10LkUt_AcPWlNyPDiVGfo67u3X5oPxerj-_NmuSosZzUralmLtnXcAK1sSxzlvGoFsRsqS6kEEYKXzCruJJGSbpRwm9IKUK4VYIg1fIbOjt7dfrMFZ6Hrkwl6l_x2PEdH4_W_k85f6u_xWldVyTmRo-D1SZDijz3kXm99thCC6SDus5Zc0LJm4kC-OZI2xZwTtPdbKNGHGPQYg76LYWRfPTzrL3n6-wgsjsBPH2D4v0k3q-aovAXmepOj</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Borges, Flávia K.</creator><creator>Borges, Fernando K.</creator><creator>Stella, Steffan F.</creator><creator>Souza, Juliana F.</creator><creator>Wendland, Andréa E.</creator><creator>Werres Junior, Luis Carlos</creator><creator>Ribeiro, Jorge P.</creator><creator>Polanczyk, Carísi A.</creator><general>Wiley Periodicals, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200911</creationdate><title>Serial Analyses of C‐Reactive Protein and Myeloperoxidase in Acute Coronary Syndrome</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3292-9794ffd3ae16cf0d1336f40cb175784044352c83d70771b84db5c4e8df4ea0ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Coronary Syndrome - enzymology</topic><topic>Acute Coronary Syndrome - immunology</topic><topic>Acute Coronary Syndrome - mortality</topic><topic>Acute Coronary Syndrome - therapy</topic><topic>Aged</topic><topic>Biomarkers - blood</topic><topic>C-Reactive Protein - metabolism</topic><topic>Case Report</topic><topic>Case Reports</topic><topic>Female</topic><topic>Humans</topic><topic>inflammation</topic><topic>Inflammation Mediators - blood</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>markers</topic><topic>Middle Aged</topic><topic>myocardial infarction</topic><topic>Peroxidase - blood</topic><topic>prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>unstable angina</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical cardiology (Mahwah, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borges, Flávia K.</au><au>Borges, Fernando K.</au><au>Stella, Steffan F.</au><au>Souza, Juliana F.</au><au>Wendland, Andréa E.</au><au>Werres Junior, Luis Carlos</au><au>Ribeiro, Jorge P.</au><au>Polanczyk, Carísi A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serial Analyses of C‐Reactive Protein and Myeloperoxidase in Acute Coronary Syndrome</atitle><jtitle>Clinical cardiology (Mahwah, N.J.)</jtitle><addtitle>Clin Cardiol</addtitle><date>2009-11</date><risdate>2009</risdate><volume>32</volume><issue>11</issue><spage>E58</spage><epage>E62</epage><pages>E58-E62</pages><issn>0160-9289</issn><issn>1932-8737</issn><eissn>1932-8737</eissn><abstract>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.</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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