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Platelet-bound cyclophilin A in patients with stable coronary artery disease and acute myocardial infarction
Objective: Recently, we reported that extracellular cyclophilin A (CyPA) is an important agonist for platelets. Whereas soluble CyPA-levels have been associated with cardiovascular risk factors, cell-bound CyPA has not been investigated yet. In this study, we analyzed for the first time platelet-bou...
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Published in: | Platelets (Edinburgh) 2016-02, Vol.27 (2), p.155-158 |
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description | Objective: Recently, we reported that extracellular cyclophilin A (CyPA) is an important agonist for platelets. Whereas soluble CyPA-levels have been associated with cardiovascular risk factors, cell-bound CyPA has not been investigated yet. In this study, we analyzed for the first time platelet-bound CyPA in patients with symptomatic coronary artery disease (CAD). Methods and results: blood was obtained from 388 consecutive patients: 204 with stable CAD and 184 with acute coronary syndrome (76 with unstable angina, 78 with non ST-elevation myocardial infarction (NSTEMI), and 30 with STEMI). In vitro stimulation of platelets with classical agonists revealed an enhanced expression of CyPA on the platelet surface. In patients with stable CAD, platelet-bound CyPA correlated excellently with platelet activity measured by P-selectin exposure in flow cytometry. The analysis of classical risk factors for atherosclerosis revealed that patients with hypertension and hypercholesterolemia had significantly enhanced platelet-bound CyPA, whereas diabetes and smoking were not associated with enhanced CyPA-binding to the platelet surface. In multivariate analysis, hypercholesterolemia was the only significant predictor of enhanced platelet-bound CyPA. Interestingly, in patients with acute myocardial infarction (AMI) platelet-bound CyPA was significantly decreased compared with patients with stable CAD. Conclusions: Enhanced platelet-bound CyPA is associated with hypertension and hypercholesterolemia in stable CAD patients. In patients with AMI platelet-bound CyPA is significantly decreased. |
doi_str_mv | 10.3109/09537104.2015.1051466 |
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Whereas soluble CyPA-levels have been associated with cardiovascular risk factors, cell-bound CyPA has not been investigated yet. In this study, we analyzed for the first time platelet-bound CyPA in patients with symptomatic coronary artery disease (CAD). Methods and results: blood was obtained from 388 consecutive patients: 204 with stable CAD and 184 with acute coronary syndrome (76 with unstable angina, 78 with non ST-elevation myocardial infarction (NSTEMI), and 30 with STEMI). In vitro stimulation of platelets with classical agonists revealed an enhanced expression of CyPA on the platelet surface. In patients with stable CAD, platelet-bound CyPA correlated excellently with platelet activity measured by P-selectin exposure in flow cytometry. The analysis of classical risk factors for atherosclerosis revealed that patients with hypertension and hypercholesterolemia had significantly enhanced platelet-bound CyPA, whereas diabetes and smoking were not associated with enhanced CyPA-binding to the platelet surface. In multivariate analysis, hypercholesterolemia was the only significant predictor of enhanced platelet-bound CyPA. Interestingly, in patients with acute myocardial infarction (AMI) platelet-bound CyPA was significantly decreased compared with patients with stable CAD. Conclusions: Enhanced platelet-bound CyPA is associated with hypertension and hypercholesterolemia in stable CAD patients. In patients with AMI platelet-bound CyPA is significantly decreased.</description><identifier>ISSN: 0953-7104</identifier><identifier>EISSN: 1369-1635</identifier><identifier>DOI: 10.3109/09537104.2015.1051466</identifier><identifier>PMID: 26084004</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Acute coronary syndrome ; Aged ; Aged, 80 and over ; Angina, Unstable - blood ; Angina, Unstable - complications ; Angina, Unstable - pathology ; Blood Platelets - metabolism ; Blood Platelets - pathology ; Coronary Artery Disease - blood ; Coronary Artery Disease - complications ; Coronary Artery Disease - pathology ; Cyclophilin A ; Cyclophilin A - blood ; Cyclophilin A - genetics ; Diabetes Mellitus - physiopathology ; Female ; Gene Expression ; Humans ; Hypercholesterolemia - blood ; Hypercholesterolemia - complications ; Hypercholesterolemia - pathology ; Hypertension - blood ; Hypertension - complications ; Hypertension - pathology ; Male ; Middle Aged ; P-Selectin - blood ; P-Selectin - genetics ; Platelet Activation ; platelets ; Protein Binding ; Risk Factors ; Smoking - physiopathology ; thrombosis</subject><ispartof>Platelets (Edinburgh), 2016-02, Vol.27 (2), p.155-158</ispartof><rights>2015 Taylor & Francis Group, LLC. 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-32a6c6147263e90c724b98387dd36b906f0d12b266e0d1c4580ba801f39c1e193</citedby><cites>FETCH-LOGICAL-c436t-32a6c6147263e90c724b98387dd36b906f0d12b266e0d1c4580ba801f39c1e193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26084004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seizer, Peter</creatorcontrib><creatorcontrib>Fuchs, Christian</creatorcontrib><creatorcontrib>Ungern-Sternberg, Saskia N.I. v.</creatorcontrib><creatorcontrib>Heinzmann, David</creatorcontrib><creatorcontrib>Langer, Harald</creatorcontrib><creatorcontrib>Gawaz, Meinrad</creatorcontrib><creatorcontrib>May, Andreas E.</creatorcontrib><creatorcontrib>Geisler, Tobias</creatorcontrib><title>Platelet-bound cyclophilin A in patients with stable coronary artery disease and acute myocardial infarction</title><title>Platelets (Edinburgh)</title><addtitle>Platelets</addtitle><description>Objective: Recently, we reported that extracellular cyclophilin A (CyPA) is an important agonist for platelets. Whereas soluble CyPA-levels have been associated with cardiovascular risk factors, cell-bound CyPA has not been investigated yet. In this study, we analyzed for the first time platelet-bound CyPA in patients with symptomatic coronary artery disease (CAD). Methods and results: blood was obtained from 388 consecutive patients: 204 with stable CAD and 184 with acute coronary syndrome (76 with unstable angina, 78 with non ST-elevation myocardial infarction (NSTEMI), and 30 with STEMI). In vitro stimulation of platelets with classical agonists revealed an enhanced expression of CyPA on the platelet surface. In patients with stable CAD, platelet-bound CyPA correlated excellently with platelet activity measured by P-selectin exposure in flow cytometry. The analysis of classical risk factors for atherosclerosis revealed that patients with hypertension and hypercholesterolemia had significantly enhanced platelet-bound CyPA, whereas diabetes and smoking were not associated with enhanced CyPA-binding to the platelet surface. In multivariate analysis, hypercholesterolemia was the only significant predictor of enhanced platelet-bound CyPA. Interestingly, in patients with acute myocardial infarction (AMI) platelet-bound CyPA was significantly decreased compared with patients with stable CAD. Conclusions: Enhanced platelet-bound CyPA is associated with hypertension and hypercholesterolemia in stable CAD patients. In patients with AMI platelet-bound CyPA is significantly decreased.</description><subject>Acute coronary syndrome</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Angina, Unstable - blood</subject><subject>Angina, Unstable - complications</subject><subject>Angina, Unstable - pathology</subject><subject>Blood Platelets - metabolism</subject><subject>Blood Platelets - pathology</subject><subject>Coronary Artery Disease - blood</subject><subject>Coronary Artery Disease - complications</subject><subject>Coronary Artery Disease - pathology</subject><subject>Cyclophilin A</subject><subject>Cyclophilin A - blood</subject><subject>Cyclophilin A - genetics</subject><subject>Diabetes Mellitus - physiopathology</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Hypercholesterolemia - blood</subject><subject>Hypercholesterolemia - complications</subject><subject>Hypercholesterolemia - pathology</subject><subject>Hypertension - blood</subject><subject>Hypertension - complications</subject><subject>Hypertension - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>P-Selectin - blood</subject><subject>P-Selectin - genetics</subject><subject>Platelet Activation</subject><subject>platelets</subject><subject>Protein Binding</subject><subject>Risk Factors</subject><subject>Smoking - physiopathology</subject><subject>thrombosis</subject><issn>0953-7104</issn><issn>1369-1635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhi3UCpaPnwDysZdsx7HjxDcQaqESUntoz9bEcYSREy-2I7T_vo524chlZg7PvKN5CLlmsOUM1HdQDW8ZiG0NrNkyaJiQ8oRsGJeqYpI3X8hmZaoVOiPnKb0AsA5kc0rOagmdABAb4v94zNbbXPVhmQdq9saH3bPzbqZ3tJQdZmfnnOiby880Zey9pSbEMGPcU4zZlja4ZDFZiiUBzZItnfbBYBwc-hIyYjTZhfmSfB3RJ3t17Bfk388ff-8fq6ffD7_u754qI7jMFa9RGslEW0tuFZi2Fr3qeNcOA5e9AjnCwOq-ltKWwYimgx47YCNXhlmm-AX5dsjdxfC62JT15JKx3uNsw5I0a2WrWKNAFLQ5oCaGlKId9S66qbymGehVtH4XrVfR-ii67N0cTyz9ZIePrXezBbg9AOX9ECd8C9EPOuPehzhGnI1La_5nN_4DakyNUg</recordid><startdate>20160217</startdate><enddate>20160217</enddate><creator>Seizer, Peter</creator><creator>Fuchs, Christian</creator><creator>Ungern-Sternberg, Saskia N.I. v.</creator><creator>Heinzmann, David</creator><creator>Langer, Harald</creator><creator>Gawaz, Meinrad</creator><creator>May, Andreas E.</creator><creator>Geisler, Tobias</creator><general>Informa Healthcare</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></search><sort><creationdate>20160217</creationdate><title>Platelet-bound cyclophilin A in patients with stable coronary artery disease and acute myocardial infarction</title><author>Seizer, Peter ; Fuchs, Christian ; Ungern-Sternberg, Saskia N.I. v. ; Heinzmann, David ; Langer, Harald ; Gawaz, Meinrad ; May, Andreas E. ; Geisler, Tobias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-32a6c6147263e90c724b98387dd36b906f0d12b266e0d1c4580ba801f39c1e193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute coronary syndrome</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Angina, Unstable - blood</topic><topic>Angina, Unstable - complications</topic><topic>Angina, Unstable - pathology</topic><topic>Blood Platelets - metabolism</topic><topic>Blood Platelets - pathology</topic><topic>Coronary Artery Disease - blood</topic><topic>Coronary Artery Disease - complications</topic><topic>Coronary Artery Disease - pathology</topic><topic>Cyclophilin A</topic><topic>Cyclophilin A - blood</topic><topic>Cyclophilin A - genetics</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Hypercholesterolemia - blood</topic><topic>Hypercholesterolemia - complications</topic><topic>Hypercholesterolemia - pathology</topic><topic>Hypertension - blood</topic><topic>Hypertension - complications</topic><topic>Hypertension - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>P-Selectin - blood</topic><topic>P-Selectin - genetics</topic><topic>Platelet Activation</topic><topic>platelets</topic><topic>Protein Binding</topic><topic>Risk Factors</topic><topic>Smoking - physiopathology</topic><topic>thrombosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seizer, Peter</creatorcontrib><creatorcontrib>Fuchs, Christian</creatorcontrib><creatorcontrib>Ungern-Sternberg, Saskia N.I. v.</creatorcontrib><creatorcontrib>Heinzmann, David</creatorcontrib><creatorcontrib>Langer, Harald</creatorcontrib><creatorcontrib>Gawaz, Meinrad</creatorcontrib><creatorcontrib>May, Andreas E.</creatorcontrib><creatorcontrib>Geisler, Tobias</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><jtitle>Platelets (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seizer, Peter</au><au>Fuchs, Christian</au><au>Ungern-Sternberg, Saskia N.I. v.</au><au>Heinzmann, David</au><au>Langer, Harald</au><au>Gawaz, Meinrad</au><au>May, Andreas E.</au><au>Geisler, Tobias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Platelet-bound cyclophilin A in patients with stable coronary artery disease and acute myocardial infarction</atitle><jtitle>Platelets (Edinburgh)</jtitle><addtitle>Platelets</addtitle><date>2016-02-17</date><risdate>2016</risdate><volume>27</volume><issue>2</issue><spage>155</spage><epage>158</epage><pages>155-158</pages><issn>0953-7104</issn><eissn>1369-1635</eissn><abstract>Objective: Recently, we reported that extracellular cyclophilin A (CyPA) is an important agonist for platelets. Whereas soluble CyPA-levels have been associated with cardiovascular risk factors, cell-bound CyPA has not been investigated yet. In this study, we analyzed for the first time platelet-bound CyPA in patients with symptomatic coronary artery disease (CAD). Methods and results: blood was obtained from 388 consecutive patients: 204 with stable CAD and 184 with acute coronary syndrome (76 with unstable angina, 78 with non ST-elevation myocardial infarction (NSTEMI), and 30 with STEMI). In vitro stimulation of platelets with classical agonists revealed an enhanced expression of CyPA on the platelet surface. In patients with stable CAD, platelet-bound CyPA correlated excellently with platelet activity measured by P-selectin exposure in flow cytometry. The analysis of classical risk factors for atherosclerosis revealed that patients with hypertension and hypercholesterolemia had significantly enhanced platelet-bound CyPA, whereas diabetes and smoking were not associated with enhanced CyPA-binding to the platelet surface. In multivariate analysis, hypercholesterolemia was the only significant predictor of enhanced platelet-bound CyPA. Interestingly, in patients with acute myocardial infarction (AMI) platelet-bound CyPA was significantly decreased compared with patients with stable CAD. Conclusions: Enhanced platelet-bound CyPA is associated with hypertension and hypercholesterolemia in stable CAD patients. In patients with AMI platelet-bound CyPA is significantly decreased.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>26084004</pmid><doi>10.3109/09537104.2015.1051466</doi><tpages>4</tpages></addata></record> |
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subjects | Acute coronary syndrome Aged Aged, 80 and over Angina, Unstable - blood Angina, Unstable - complications Angina, Unstable - pathology Blood Platelets - metabolism Blood Platelets - pathology Coronary Artery Disease - blood Coronary Artery Disease - complications Coronary Artery Disease - pathology Cyclophilin A Cyclophilin A - blood Cyclophilin A - genetics Diabetes Mellitus - physiopathology Female Gene Expression Humans Hypercholesterolemia - blood Hypercholesterolemia - complications Hypercholesterolemia - pathology Hypertension - blood Hypertension - complications Hypertension - pathology Male Middle Aged P-Selectin - blood P-Selectin - genetics Platelet Activation platelets Protein Binding Risk Factors Smoking - physiopathology thrombosis |
title | Platelet-bound cyclophilin A in patients with stable coronary artery disease and acute myocardial infarction |
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