No Association between Thrombin Generation and Intra-Plaque Haemorrhage in Symptomatic Carotid Atherosclerotic Plaques: The Plaque at RISK (PARISK) Study

Abstract Background  Carotid atherosclerosis is an important cause of stroke. Intra-plaque haemorrhage (IPH) on magnetic resonance imaging (MRI) increases stroke risk. Development of IPH is only partly understood. Thrombin is an essential enzyme in haemostasis. Experimental animal studies have shown...

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Veröffentlicht in:Thrombosis and haemostasis 2018-08, Vol.118 (8), p.1461-1469
Hauptverfasser: Crombag, Geneviève A. J. C., Spronk, Henri M., Nelemans, Patty, Schreuder, Floris H. B. M., Truijman, Martine T. B., van Dijk, Anouk C., de Rotte, Alexandra A. J., Liem, Madieke I., Daemen, Mat J. A. P., van der Steen, Anton F. W., Mess, Werner H., Nederkoorn, Paul J., Hendrikse, Jeroen, van der Lugt, Aad, Wildberger, Joachim E., ten Cate, Hugo, van Oostenbrugge, Robert J., Kooi, M. Eline
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container_end_page 1469
container_issue 8
container_start_page 1461
container_title Thrombosis and haemostasis
container_volume 118
creator Crombag, Geneviève A. J. C.
Spronk, Henri M.
Nelemans, Patty
Schreuder, Floris H. B. M.
Truijman, Martine T. B.
van Dijk, Anouk C.
de Rotte, Alexandra A. J.
Liem, Madieke I.
Daemen, Mat J. A. P.
van der Steen, Anton F. W.
Mess, Werner H.
Nederkoorn, Paul J.
Hendrikse, Jeroen
van der Lugt, Aad
Wildberger, Joachim E.
ten Cate, Hugo
van Oostenbrugge, Robert J.
Kooi, M. Eline
description Abstract Background  Carotid atherosclerosis is an important cause of stroke. Intra-plaque haemorrhage (IPH) on magnetic resonance imaging (MRI) increases stroke risk. Development of IPH is only partly understood. Thrombin is an essential enzyme in haemostasis. Experimental animal studies have shown conflicting results on the relation between thrombin and plaque vulnerability. We hypothesize that decreased thrombin generation (TG) is associated with IPH and plaque vulnerability. Objective  This article investigates whether TG is associated with IPH and other features of plaque vulnerability in stroke patients. Methods  Recently symptomatic stroke patients underwent carotid MRI and blood sampling. MRI plaque features include plaque burden, presence of IPH, amount of lipid-rich necrotic core (LRNC), calcified tissue and fibrous tissue (% of total wall volume). TG was assessed in platelet-poor plasma and expressed as: peak height (PH) and endogenous thrombin potential (ETP). MR images could be analysed in 224 patients. Blood samples were available in 161 of 224 patients. Binary multivariate logistic and linear regression were used to investigate the association between TG and MRI plaque features. Results  IPH and LRNC were present in 65 (40%) and 102 (63%) of plaques. There were no significant associations between TG and IPH; PH odds ratio (OR) = 1, 95% confidence interval (CI): 0.76 to 1.45 and ETP OR = 1, 95% CI: 0.73 to 1.37. After correction for age, sex and hypercholesterolaemia, the association was weak but non-significant; PH: OR = 0.76, 95% CI: 0.52 to 1.10 and ETP: OR = 0.73, 95% CI: 0.53 to 1.37. Conclusion  Features of carotid plaque on MRI show no significant association with TG in stroke patients. Systemic TG does not seem to be an important factor in IPH development.
doi_str_mv 10.1055/s-0038-1666858
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J. C. ; Spronk, Henri M. ; Nelemans, Patty ; Schreuder, Floris H. B. M. ; Truijman, Martine T. B. ; van Dijk, Anouk C. ; de Rotte, Alexandra A. J. ; Liem, Madieke I. ; Daemen, Mat J. A. P. ; van der Steen, Anton F. W. ; Mess, Werner H. ; Nederkoorn, Paul J. ; Hendrikse, Jeroen ; van der Lugt, Aad ; Wildberger, Joachim E. ; ten Cate, Hugo ; van Oostenbrugge, Robert J. ; Kooi, M. Eline</creator><creatorcontrib>Crombag, Geneviève A. J. C. ; Spronk, Henri M. ; Nelemans, Patty ; Schreuder, Floris H. B. M. ; Truijman, Martine T. B. ; van Dijk, Anouk C. ; de Rotte, Alexandra A. J. ; Liem, Madieke I. ; Daemen, Mat J. A. P. ; van der Steen, Anton F. W. ; Mess, Werner H. ; Nederkoorn, Paul J. ; Hendrikse, Jeroen ; van der Lugt, Aad ; Wildberger, Joachim E. ; ten Cate, Hugo ; van Oostenbrugge, Robert J. ; Kooi, M. Eline</creatorcontrib><description>Abstract Background  Carotid atherosclerosis is an important cause of stroke. Intra-plaque haemorrhage (IPH) on magnetic resonance imaging (MRI) increases stroke risk. Development of IPH is only partly understood. Thrombin is an essential enzyme in haemostasis. Experimental animal studies have shown conflicting results on the relation between thrombin and plaque vulnerability. We hypothesize that decreased thrombin generation (TG) is associated with IPH and plaque vulnerability. Objective  This article investigates whether TG is associated with IPH and other features of plaque vulnerability in stroke patients. Methods  Recently symptomatic stroke patients underwent carotid MRI and blood sampling. MRI plaque features include plaque burden, presence of IPH, amount of lipid-rich necrotic core (LRNC), calcified tissue and fibrous tissue (% of total wall volume). TG was assessed in platelet-poor plasma and expressed as: peak height (PH) and endogenous thrombin potential (ETP). MR images could be analysed in 224 patients. Blood samples were available in 161 of 224 patients. Binary multivariate logistic and linear regression were used to investigate the association between TG and MRI plaque features. Results  IPH and LRNC were present in 65 (40%) and 102 (63%) of plaques. There were no significant associations between TG and IPH; PH odds ratio (OR) = 1, 95% confidence interval (CI): 0.76 to 1.45 and ETP OR = 1, 95% CI: 0.73 to 1.37. After correction for age, sex and hypercholesterolaemia, the association was weak but non-significant; PH: OR = 0.76, 95% CI: 0.52 to 1.10 and ETP: OR = 0.73, 95% CI: 0.53 to 1.37. Conclusion  Features of carotid plaque on MRI show no significant association with TG in stroke patients. Systemic TG does not seem to be an important factor in IPH development.</description><identifier>ISSN: 0340-6245</identifier><identifier>EISSN: 2567-689X</identifier><identifier>DOI: 10.1055/s-0038-1666858</identifier><identifier>PMID: 29972860</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag KG</publisher><subject>Atherosclerosis and Ischaemic Disease</subject><ispartof>Thrombosis and haemostasis, 2018-08, Vol.118 (8), p.1461-1469</ispartof><rights>Georg Thieme Verlag KG Stuttgart · New York.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-b64bad7b5ea23e8c89e8d668190a475450a2b6a014526578e6b3aa63ec7a07c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0038-1666858.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0038-1666858$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3003,3004,27903,27904,54537,54538</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29972860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Crombag, Geneviève A. J. C.</creatorcontrib><creatorcontrib>Spronk, Henri M.</creatorcontrib><creatorcontrib>Nelemans, Patty</creatorcontrib><creatorcontrib>Schreuder, Floris H. B. M.</creatorcontrib><creatorcontrib>Truijman, Martine T. B.</creatorcontrib><creatorcontrib>van Dijk, Anouk C.</creatorcontrib><creatorcontrib>de Rotte, Alexandra A. J.</creatorcontrib><creatorcontrib>Liem, Madieke I.</creatorcontrib><creatorcontrib>Daemen, Mat J. A. P.</creatorcontrib><creatorcontrib>van der Steen, Anton F. W.</creatorcontrib><creatorcontrib>Mess, Werner H.</creatorcontrib><creatorcontrib>Nederkoorn, Paul J.</creatorcontrib><creatorcontrib>Hendrikse, Jeroen</creatorcontrib><creatorcontrib>van der Lugt, Aad</creatorcontrib><creatorcontrib>Wildberger, Joachim E.</creatorcontrib><creatorcontrib>ten Cate, Hugo</creatorcontrib><creatorcontrib>van Oostenbrugge, Robert J.</creatorcontrib><creatorcontrib>Kooi, M. Eline</creatorcontrib><title>No Association between Thrombin Generation and Intra-Plaque Haemorrhage in Symptomatic Carotid Atherosclerotic Plaques: The Plaque at RISK (PARISK) Study</title><title>Thrombosis and haemostasis</title><addtitle>Thromb Haemost</addtitle><description>Abstract Background  Carotid atherosclerosis is an important cause of stroke. Intra-plaque haemorrhage (IPH) on magnetic resonance imaging (MRI) increases stroke risk. Development of IPH is only partly understood. Thrombin is an essential enzyme in haemostasis. Experimental animal studies have shown conflicting results on the relation between thrombin and plaque vulnerability. We hypothesize that decreased thrombin generation (TG) is associated with IPH and plaque vulnerability. Objective  This article investigates whether TG is associated with IPH and other features of plaque vulnerability in stroke patients. Methods  Recently symptomatic stroke patients underwent carotid MRI and blood sampling. MRI plaque features include plaque burden, presence of IPH, amount of lipid-rich necrotic core (LRNC), calcified tissue and fibrous tissue (% of total wall volume). TG was assessed in platelet-poor plasma and expressed as: peak height (PH) and endogenous thrombin potential (ETP). MR images could be analysed in 224 patients. Blood samples were available in 161 of 224 patients. Binary multivariate logistic and linear regression were used to investigate the association between TG and MRI plaque features. Results  IPH and LRNC were present in 65 (40%) and 102 (63%) of plaques. There were no significant associations between TG and IPH; PH odds ratio (OR) = 1, 95% confidence interval (CI): 0.76 to 1.45 and ETP OR = 1, 95% CI: 0.73 to 1.37. After correction for age, sex and hypercholesterolaemia, the association was weak but non-significant; PH: OR = 0.76, 95% CI: 0.52 to 1.10 and ETP: OR = 0.73, 95% CI: 0.53 to 1.37. Conclusion  Features of carotid plaque on MRI show no significant association with TG in stroke patients. Systemic TG does not seem to be an important factor in IPH development.</description><subject>Atherosclerosis and Ischaemic Disease</subject><issn>0340-6245</issn><issn>2567-689X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PAjEQhhujEUSvHk2Peih2P9rteiNEgUiUCAdvm9nuIEvYLbYlhp_iv3XJojdPk8k870z7EHId8H7Ahbh3jPNIsUBKqYQ6Id1QyIRJlb6fki6PYs5kGIsOuXBuzXkg41Sck06YpkmoJO-S7xdDB84ZXYIvTU1z9F-INV2srKnysqYjrNG2M6gLOqm9BTbbwOcO6RiwMtau4ANpg8731dabqoE1HYI1vizowK_QGqc3eOg1bZPuoTmAx4aCp2-T-TO9nQ0O9Y7O_a7YX5KzJWwcXh1rjyyeHhfDMZu-jibDwZTpKIk8y2WcQ5HkAiGMUGmVoioaGUHKIU5ELDiEuQQexCKUIlEo8whARqgT4ImOeqTfrtXNM53FZba1ZQV2nwU8OyjOXHZQnB0VN4GbNrDd5RUWf_iv0wZgLeBXJVaYrc3O1s0P_lv4Ayqrhok</recordid><startdate>201808</startdate><enddate>201808</enddate><creator>Crombag, Geneviève A. J. C.</creator><creator>Spronk, Henri M.</creator><creator>Nelemans, Patty</creator><creator>Schreuder, Floris H. B. M.</creator><creator>Truijman, Martine T. B.</creator><creator>van Dijk, Anouk C.</creator><creator>de Rotte, Alexandra A. J.</creator><creator>Liem, Madieke I.</creator><creator>Daemen, Mat J. A. P.</creator><creator>van der Steen, Anton F. W.</creator><creator>Mess, Werner H.</creator><creator>Nederkoorn, Paul J.</creator><creator>Hendrikse, Jeroen</creator><creator>van der Lugt, Aad</creator><creator>Wildberger, Joachim E.</creator><creator>ten Cate, Hugo</creator><creator>van Oostenbrugge, Robert J.</creator><creator>Kooi, M. 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W.</creatorcontrib><creatorcontrib>Mess, Werner H.</creatorcontrib><creatorcontrib>Nederkoorn, Paul J.</creatorcontrib><creatorcontrib>Hendrikse, Jeroen</creatorcontrib><creatorcontrib>van der Lugt, Aad</creatorcontrib><creatorcontrib>Wildberger, Joachim E.</creatorcontrib><creatorcontrib>ten Cate, Hugo</creatorcontrib><creatorcontrib>van Oostenbrugge, Robert J.</creatorcontrib><creatorcontrib>Kooi, M. Eline</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Crombag, Geneviève A. J. C.</au><au>Spronk, Henri M.</au><au>Nelemans, Patty</au><au>Schreuder, Floris H. B. M.</au><au>Truijman, Martine T. B.</au><au>van Dijk, Anouk C.</au><au>de Rotte, Alexandra A. J.</au><au>Liem, Madieke I.</au><au>Daemen, Mat J. A. P.</au><au>van der Steen, Anton F. W.</au><au>Mess, Werner H.</au><au>Nederkoorn, Paul J.</au><au>Hendrikse, Jeroen</au><au>van der Lugt, Aad</au><au>Wildberger, Joachim E.</au><au>ten Cate, Hugo</au><au>van Oostenbrugge, Robert J.</au><au>Kooi, M. Eline</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>No Association between Thrombin Generation and Intra-Plaque Haemorrhage in Symptomatic Carotid Atherosclerotic Plaques: The Plaque at RISK (PARISK) Study</atitle><jtitle>Thrombosis and haemostasis</jtitle><addtitle>Thromb Haemost</addtitle><date>2018-08</date><risdate>2018</risdate><volume>118</volume><issue>8</issue><spage>1461</spage><epage>1469</epage><pages>1461-1469</pages><issn>0340-6245</issn><eissn>2567-689X</eissn><abstract>Abstract Background  Carotid atherosclerosis is an important cause of stroke. Intra-plaque haemorrhage (IPH) on magnetic resonance imaging (MRI) increases stroke risk. Development of IPH is only partly understood. Thrombin is an essential enzyme in haemostasis. Experimental animal studies have shown conflicting results on the relation between thrombin and plaque vulnerability. We hypothesize that decreased thrombin generation (TG) is associated with IPH and plaque vulnerability. Objective  This article investigates whether TG is associated with IPH and other features of plaque vulnerability in stroke patients. Methods  Recently symptomatic stroke patients underwent carotid MRI and blood sampling. MRI plaque features include plaque burden, presence of IPH, amount of lipid-rich necrotic core (LRNC), calcified tissue and fibrous tissue (% of total wall volume). TG was assessed in platelet-poor plasma and expressed as: peak height (PH) and endogenous thrombin potential (ETP). MR images could be analysed in 224 patients. Blood samples were available in 161 of 224 patients. Binary multivariate logistic and linear regression were used to investigate the association between TG and MRI plaque features. Results  IPH and LRNC were present in 65 (40%) and 102 (63%) of plaques. There were no significant associations between TG and IPH; PH odds ratio (OR) = 1, 95% confidence interval (CI): 0.76 to 1.45 and ETP OR = 1, 95% CI: 0.73 to 1.37. After correction for age, sex and hypercholesterolaemia, the association was weak but non-significant; PH: OR = 0.76, 95% CI: 0.52 to 1.10 and ETP: OR = 0.73, 95% CI: 0.53 to 1.37. Conclusion  Features of carotid plaque on MRI show no significant association with TG in stroke patients. Systemic TG does not seem to be an important factor in IPH development.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag KG</pub><pmid>29972860</pmid><doi>10.1055/s-0038-1666858</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Atherosclerosis and Ischaemic Disease
title No Association between Thrombin Generation and Intra-Plaque Haemorrhage in Symptomatic Carotid Atherosclerotic Plaques: The Plaque at RISK (PARISK) Study
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