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Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction
Background Early detection of acute myocardial infarction (AMI) using cardiac biomarkers of myocardial necrosis remains limited since these biomarkers do not rise within the first hours from onset of AMI. We aimed to compare the temporal release pattern of the C-terminal portion of provasopressin (c...
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Published in: | Clinical research in cardiology 2011-12, Vol.100 (12), p.1069-1076 |
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container_title | Clinical research in cardiology |
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creator | Gu, Youlan L. Voors, Adriaan A. Zijlstra, Felix Hillege, Hans L. Struck, Joachim Masson, Serge Vago, Tarcisio Anker, Stefan D. van den Heuvel, Ad F. M. van Veldhuisen, Dirk J. de Smet, Bart J. G. L. |
description | Background
Early detection of acute myocardial infarction (AMI) using cardiac biomarkers of myocardial necrosis remains limited since these biomarkers do not rise within the first hours from onset of AMI. We aimed to compare the temporal release pattern of the C-terminal portion of provasopressin (copeptin) with conventional cardiac biomarkers, including creatine kinase isoenzyme (CK-MB), cardiac troponin T (cTnT), and high-sensitivity cTnT (hs-cTnT), in patients with ST-elevation AMI.
Methods
We included 145 patients undergoing successful primary percutaneous coronary intervention (PCI) for a first ST-elevation AMI presenting within 12 h of symptom onset. Blood samples were taken on admission and at four time points within the first 24 h after PCI.
Results
In contrast to all other markers, copeptin levels were already elevated on admission and were higher with a shorter time from symptom onset to reperfusion and lower systolic blood pressure. Copeptin levels peaked immediately after symptom onset at a maximum of 249 pmol/L and normalized within 10 h. In contrast, CK-MB, cTnT, and hs-cTnT peaked after 14 h from symptom onset at a maximum of 275 U/L, 5.75 μg/L, and 4.16 μg/L, respectively, and decreased more gradually.
Conclusions
Copeptin has a distinct release pattern in patients with ST-elevation AMI, peaking within the first hour after symptom onset before conventional cardiac biomarkers and falling to normal ranges within the first day. Further studies are required to determine the exact role of copeptin in AMI suspects presenting within the first hours after symptom onset. |
doi_str_mv | 10.1007/s00392-011-0343-y |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3222827</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2517728581</sourcerecordid><originalsourceid>FETCH-LOGICAL-c468t-ebd024c7a6b4eecf8ad45d5cf1b5ceb9a19723d4cc8d1d6f5414714b2502474e3</originalsourceid><addsrcrecordid>eNp1kU9P3DAQxS0EAgp8AC4o4tJTiu04TnKpVK36T0LiAmfLcSa7pomd2g5ov31n2WVLK3GyR-83zzN-hFwy-olRWt1ESouG55SxnBaiyNcH5JTVEivZ8MP9vRYn5EOMj5SWDLljcsJZJSUvmlMSFn6cdLDRu8z3WVpBlmCcfNBDFmAAHSGbdEoQXnTjJ5iSddmzTSus3BO4ZL1DurV-1OEXhJihrs2cIBvX3ujQWZSt63UwG_acHPV6iHCxO8_Iw7ev94sf-e3d95-LL7e5EbJOObQd5cJUWrYCwPS17kTZlaZnbWmgbTRrKl50wpi6Y53sS8FExUTLS2yrBBRn5PPWd5rbETqDk-JWagoW51wrr636V3F2pZb-SRWc85pXaPBxZxD87xliUqONBoZBO_BzVA0tG8lpI5G8_o989HPAX3mBKol2BUJsC5ngYwzQ70dhVG3yVNs8FeapNnmqNfZcvd1h3_EaIAJ8C0SU3BLC35ffd_0DwO6vqg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>905762823</pqid></control><display><type>article</type><title>Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction</title><source>Springer Nature</source><creator>Gu, Youlan L. ; Voors, Adriaan A. ; Zijlstra, Felix ; Hillege, Hans L. ; Struck, Joachim ; Masson, Serge ; Vago, Tarcisio ; Anker, Stefan D. ; van den Heuvel, Ad F. M. ; van Veldhuisen, Dirk J. ; de Smet, Bart J. G. L.</creator><creatorcontrib>Gu, Youlan L. ; Voors, Adriaan A. ; Zijlstra, Felix ; Hillege, Hans L. ; Struck, Joachim ; Masson, Serge ; Vago, Tarcisio ; Anker, Stefan D. ; van den Heuvel, Ad F. M. ; van Veldhuisen, Dirk J. ; de Smet, Bart J. G. L.</creatorcontrib><description>Background
Early detection of acute myocardial infarction (AMI) using cardiac biomarkers of myocardial necrosis remains limited since these biomarkers do not rise within the first hours from onset of AMI. We aimed to compare the temporal release pattern of the C-terminal portion of provasopressin (copeptin) with conventional cardiac biomarkers, including creatine kinase isoenzyme (CK-MB), cardiac troponin T (cTnT), and high-sensitivity cTnT (hs-cTnT), in patients with ST-elevation AMI.
Methods
We included 145 patients undergoing successful primary percutaneous coronary intervention (PCI) for a first ST-elevation AMI presenting within 12 h of symptom onset. Blood samples were taken on admission and at four time points within the first 24 h after PCI.
Results
In contrast to all other markers, copeptin levels were already elevated on admission and were higher with a shorter time from symptom onset to reperfusion and lower systolic blood pressure. Copeptin levels peaked immediately after symptom onset at a maximum of 249 pmol/L and normalized within 10 h. In contrast, CK-MB, cTnT, and hs-cTnT peaked after 14 h from symptom onset at a maximum of 275 U/L, 5.75 μg/L, and 4.16 μg/L, respectively, and decreased more gradually.
Conclusions
Copeptin has a distinct release pattern in patients with ST-elevation AMI, peaking within the first hour after symptom onset before conventional cardiac biomarkers and falling to normal ranges within the first day. Further studies are required to determine the exact role of copeptin in AMI suspects presenting within the first hours after symptom onset.</description><identifier>ISSN: 1861-0684</identifier><identifier>EISSN: 1861-0692</identifier><identifier>DOI: 10.1007/s00392-011-0343-y</identifier><identifier>PMID: 21766239</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Angioplasty, Balloon, Coronary ; Biomarkers - blood ; Cardiology ; Creatine Kinase, MB Form - blood ; Glycopeptides - blood ; Humans ; Medicine ; Medicine & Public Health ; Myocardial Infarction - blood ; Myocardial Infarction - diagnosis ; Myocardial Infarction - therapy ; Netherlands ; Original Paper ; Predictive Value of Tests ; Time Factors ; Treatment Outcome ; Troponin T - blood ; Up-Regulation</subject><ispartof>Clinical research in cardiology, 2011-12, Vol.100 (12), p.1069-1076</ispartof><rights>The Author(s) 2011</rights><rights>Springer-Verlag 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-ebd024c7a6b4eecf8ad45d5cf1b5ceb9a19723d4cc8d1d6f5414714b2502474e3</citedby><cites>FETCH-LOGICAL-c468t-ebd024c7a6b4eecf8ad45d5cf1b5ceb9a19723d4cc8d1d6f5414714b2502474e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21766239$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gu, Youlan L.</creatorcontrib><creatorcontrib>Voors, Adriaan A.</creatorcontrib><creatorcontrib>Zijlstra, Felix</creatorcontrib><creatorcontrib>Hillege, Hans L.</creatorcontrib><creatorcontrib>Struck, Joachim</creatorcontrib><creatorcontrib>Masson, Serge</creatorcontrib><creatorcontrib>Vago, Tarcisio</creatorcontrib><creatorcontrib>Anker, Stefan D.</creatorcontrib><creatorcontrib>van den Heuvel, Ad F. M.</creatorcontrib><creatorcontrib>van Veldhuisen, Dirk J.</creatorcontrib><creatorcontrib>de Smet, Bart J. G. L.</creatorcontrib><title>Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction</title><title>Clinical research in cardiology</title><addtitle>Clin Res Cardiol</addtitle><addtitle>Clin Res Cardiol</addtitle><description>Background
Early detection of acute myocardial infarction (AMI) using cardiac biomarkers of myocardial necrosis remains limited since these biomarkers do not rise within the first hours from onset of AMI. We aimed to compare the temporal release pattern of the C-terminal portion of provasopressin (copeptin) with conventional cardiac biomarkers, including creatine kinase isoenzyme (CK-MB), cardiac troponin T (cTnT), and high-sensitivity cTnT (hs-cTnT), in patients with ST-elevation AMI.
Methods
We included 145 patients undergoing successful primary percutaneous coronary intervention (PCI) for a first ST-elevation AMI presenting within 12 h of symptom onset. Blood samples were taken on admission and at four time points within the first 24 h after PCI.
Results
In contrast to all other markers, copeptin levels were already elevated on admission and were higher with a shorter time from symptom onset to reperfusion and lower systolic blood pressure. Copeptin levels peaked immediately after symptom onset at a maximum of 249 pmol/L and normalized within 10 h. In contrast, CK-MB, cTnT, and hs-cTnT peaked after 14 h from symptom onset at a maximum of 275 U/L, 5.75 μg/L, and 4.16 μg/L, respectively, and decreased more gradually.
Conclusions
Copeptin has a distinct release pattern in patients with ST-elevation AMI, peaking within the first hour after symptom onset before conventional cardiac biomarkers and falling to normal ranges within the first day. Further studies are required to determine the exact role of copeptin in AMI suspects presenting within the first hours after symptom onset.</description><subject>Angioplasty, Balloon, Coronary</subject><subject>Biomarkers - blood</subject><subject>Cardiology</subject><subject>Creatine Kinase, MB Form - blood</subject><subject>Glycopeptides - blood</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Myocardial Infarction - blood</subject><subject>Myocardial Infarction - diagnosis</subject><subject>Myocardial Infarction - therapy</subject><subject>Netherlands</subject><subject>Original Paper</subject><subject>Predictive Value of Tests</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Troponin T - blood</subject><subject>Up-Regulation</subject><issn>1861-0684</issn><issn>1861-0692</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kU9P3DAQxS0EAgp8AC4o4tJTiu04TnKpVK36T0LiAmfLcSa7pomd2g5ov31n2WVLK3GyR-83zzN-hFwy-olRWt1ESouG55SxnBaiyNcH5JTVEivZ8MP9vRYn5EOMj5SWDLljcsJZJSUvmlMSFn6cdLDRu8z3WVpBlmCcfNBDFmAAHSGbdEoQXnTjJ5iSddmzTSus3BO4ZL1DurV-1OEXhJihrs2cIBvX3ujQWZSt63UwG_acHPV6iHCxO8_Iw7ev94sf-e3d95-LL7e5EbJOObQd5cJUWrYCwPS17kTZlaZnbWmgbTRrKl50wpi6Y53sS8FExUTLS2yrBBRn5PPWd5rbETqDk-JWagoW51wrr636V3F2pZb-SRWc85pXaPBxZxD87xliUqONBoZBO_BzVA0tG8lpI5G8_o989HPAX3mBKol2BUJsC5ngYwzQ70dhVG3yVNs8FeapNnmqNfZcvd1h3_EaIAJ8C0SU3BLC35ffd_0DwO6vqg</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Gu, Youlan L.</creator><creator>Voors, Adriaan A.</creator><creator>Zijlstra, Felix</creator><creator>Hillege, Hans L.</creator><creator>Struck, Joachim</creator><creator>Masson, Serge</creator><creator>Vago, Tarcisio</creator><creator>Anker, Stefan D.</creator><creator>van den Heuvel, Ad F. M.</creator><creator>van Veldhuisen, Dirk J.</creator><creator>de Smet, Bart J. G. L.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20111201</creationdate><title>Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction</title><author>Gu, Youlan L. ; Voors, Adriaan A. ; Zijlstra, Felix ; Hillege, Hans L. ; Struck, Joachim ; Masson, Serge ; Vago, Tarcisio ; Anker, Stefan D. ; van den Heuvel, Ad F. M. ; van Veldhuisen, Dirk J. ; de Smet, Bart J. G. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-ebd024c7a6b4eecf8ad45d5cf1b5ceb9a19723d4cc8d1d6f5414714b2502474e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Angioplasty, Balloon, Coronary</topic><topic>Biomarkers - blood</topic><topic>Cardiology</topic><topic>Creatine Kinase, MB Form - blood</topic><topic>Glycopeptides - blood</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Myocardial Infarction - blood</topic><topic>Myocardial Infarction - diagnosis</topic><topic>Myocardial Infarction - therapy</topic><topic>Netherlands</topic><topic>Original Paper</topic><topic>Predictive Value of Tests</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Troponin T - blood</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Youlan L.</creatorcontrib><creatorcontrib>Voors, Adriaan A.</creatorcontrib><creatorcontrib>Zijlstra, Felix</creatorcontrib><creatorcontrib>Hillege, Hans L.</creatorcontrib><creatorcontrib>Struck, Joachim</creatorcontrib><creatorcontrib>Masson, Serge</creatorcontrib><creatorcontrib>Vago, Tarcisio</creatorcontrib><creatorcontrib>Anker, Stefan D.</creatorcontrib><creatorcontrib>van den Heuvel, Ad F. M.</creatorcontrib><creatorcontrib>van Veldhuisen, Dirk J.</creatorcontrib><creatorcontrib>de Smet, Bart J. G. L.</creatorcontrib><collection>Springer Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical research in cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Youlan L.</au><au>Voors, Adriaan A.</au><au>Zijlstra, Felix</au><au>Hillege, Hans L.</au><au>Struck, Joachim</au><au>Masson, Serge</au><au>Vago, Tarcisio</au><au>Anker, Stefan D.</au><au>van den Heuvel, Ad F. M.</au><au>van Veldhuisen, Dirk J.</au><au>de Smet, Bart J. G. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction</atitle><jtitle>Clinical research in cardiology</jtitle><stitle>Clin Res Cardiol</stitle><addtitle>Clin Res Cardiol</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>100</volume><issue>12</issue><spage>1069</spage><epage>1076</epage><pages>1069-1076</pages><issn>1861-0684</issn><eissn>1861-0692</eissn><abstract>Background
Early detection of acute myocardial infarction (AMI) using cardiac biomarkers of myocardial necrosis remains limited since these biomarkers do not rise within the first hours from onset of AMI. We aimed to compare the temporal release pattern of the C-terminal portion of provasopressin (copeptin) with conventional cardiac biomarkers, including creatine kinase isoenzyme (CK-MB), cardiac troponin T (cTnT), and high-sensitivity cTnT (hs-cTnT), in patients with ST-elevation AMI.
Methods
We included 145 patients undergoing successful primary percutaneous coronary intervention (PCI) for a first ST-elevation AMI presenting within 12 h of symptom onset. Blood samples were taken on admission and at four time points within the first 24 h after PCI.
Results
In contrast to all other markers, copeptin levels were already elevated on admission and were higher with a shorter time from symptom onset to reperfusion and lower systolic blood pressure. Copeptin levels peaked immediately after symptom onset at a maximum of 249 pmol/L and normalized within 10 h. In contrast, CK-MB, cTnT, and hs-cTnT peaked after 14 h from symptom onset at a maximum of 275 U/L, 5.75 μg/L, and 4.16 μg/L, respectively, and decreased more gradually.
Conclusions
Copeptin has a distinct release pattern in patients with ST-elevation AMI, peaking within the first hour after symptom onset before conventional cardiac biomarkers and falling to normal ranges within the first day. Further studies are required to determine the exact role of copeptin in AMI suspects presenting within the first hours after symptom onset.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21766239</pmid><doi>10.1007/s00392-011-0343-y</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angioplasty, Balloon, Coronary Biomarkers - blood Cardiology Creatine Kinase, MB Form - blood Glycopeptides - blood Humans Medicine Medicine & Public Health Myocardial Infarction - blood Myocardial Infarction - diagnosis Myocardial Infarction - therapy Netherlands Original Paper Predictive Value of Tests Time Factors Treatment Outcome Troponin T - blood Up-Regulation |
title | Comparison of the temporal release pattern of copeptin with conventional biomarkers in acute myocardial infarction |
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