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Intraindividual variability over time of thrombin generation in patients with cirrhosis
Patients with cirrhosis are at high risk of thrombotic events, including portal vein thrombosis and venous thromboembolism. In such patients, hypercoagulability is not detected by conventional coagulation tests, but only by the thrombin generation assay (TGA) that integrates the role of pro- and ant...
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Published in: | Journal of thrombosis and haemostasis 2023-06, Vol.21 (6), p.1441-1452 |
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container_title | Journal of thrombosis and haemostasis |
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creator | Sinegre, Thomas Duron, Cédric Lecompte, Thomas Lamblin, Géraldine Talon, Laurie Muti, Léon Massoulier, Sylvie Pereira, Bruno Lebreton, Aurélien Abergel, Armand |
description | Patients with cirrhosis are at high risk of thrombotic events, including portal vein thrombosis and venous thromboembolism. In such patients, hypercoagulability is not detected by conventional coagulation tests, but only by the thrombin generation assay (TGA) that integrates the role of pro- and anticoagulant factors. However, TGA use to predict clinical events depends on thrombin generation variability over time.
The aim of this study was to compare TGA intraindividual variability over time in patients with cirrhosis and in healthy controls.
Blood samples were prospectively collected from 34 healthy controls and 52 patients with cirrhosis at week 0 (inclusion), 6, and 12. TGA was performed with the calibrated automated thrombogram method, tissue factor (5 pM), phospholipids, and with and without thrombomodulin (4 nM) or activated protein C (1 nM).
When TGA was performed with thrombomodulin, endogenous thrombin potential in patients with cirrhosis was higher compared with controls and increased with cirrhosis severity. Stability over time of all thrombin generation parameters was excellent in healthy controls, good in Child-Turcotte-Pugh (CTP)-A patients, and poor in CTP-B/C patients (severe cirrhosis). In CTP-B/C patients, the phenotype was more variable because one-third of patients switched to normal or hypercoagulability during the 3-month follow-up.
A study with longer monitoring is needed to correlate the hypercoagulable phenotype of patients with cirrhosis with the occurrence of thrombotic events.
•Thrombin generation could be a promising tool for predicting clinical events in cirrhosis.•It is essential to know thrombin generation intraindividual variability over time.•Stability over time was good in patients with mild cirrhosis and poor in severe.•Long-term monitoring is needed to correlate hypercoagulability with thrombotic events. |
doi_str_mv | 10.1016/j.jtha.2023.02.002 |
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The aim of this study was to compare TGA intraindividual variability over time in patients with cirrhosis and in healthy controls.
Blood samples were prospectively collected from 34 healthy controls and 52 patients with cirrhosis at week 0 (inclusion), 6, and 12. TGA was performed with the calibrated automated thrombogram method, tissue factor (5 pM), phospholipids, and with and without thrombomodulin (4 nM) or activated protein C (1 nM).
When TGA was performed with thrombomodulin, endogenous thrombin potential in patients with cirrhosis was higher compared with controls and increased with cirrhosis severity. Stability over time of all thrombin generation parameters was excellent in healthy controls, good in Child-Turcotte-Pugh (CTP)-A patients, and poor in CTP-B/C patients (severe cirrhosis). In CTP-B/C patients, the phenotype was more variable because one-third of patients switched to normal or hypercoagulability during the 3-month follow-up.
A study with longer monitoring is needed to correlate the hypercoagulable phenotype of patients with cirrhosis with the occurrence of thrombotic events.
•Thrombin generation could be a promising tool for predicting clinical events in cirrhosis.•It is essential to know thrombin generation intraindividual variability over time.•Stability over time was good in patients with mild cirrhosis and poor in severe.•Long-term monitoring is needed to correlate hypercoagulability with thrombotic events.</description><identifier>ISSN: 1538-7836</identifier><identifier>ISSN: 1538-7933</identifier><identifier>EISSN: 1538-7836</identifier><identifier>DOI: 10.1016/j.jtha.2023.02.002</identifier><identifier>PMID: 36758726</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Blood Coagulation Tests - methods ; cirrhosis ; Hematology ; Human health and pathology ; Humans ; hypercoagulability ; Life Sciences ; Liver Cirrhosis - complications ; Liver Cirrhosis - diagnosis ; monitoring ; stability ; thrombin ; Thrombin - metabolism ; Thrombomodulin ; Thrombophilia ; Thrombosis</subject><ispartof>Journal of thrombosis and haemostasis, 2023-06, Vol.21 (6), p.1441-1452</ispartof><rights>2023</rights><rights>Copyright © 2023. Published by Elsevier Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-a679b3c2b379296ad45a3a4e65ebd4a78648dd56f1deb635f18a25687809463</citedby><cites>FETCH-LOGICAL-c434t-a679b3c2b379296ad45a3a4e65ebd4a78648dd56f1deb635f18a25687809463</cites><orcidid>0000-0001-7480-1052</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36758726$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-04353454$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinegre, Thomas</creatorcontrib><creatorcontrib>Duron, Cédric</creatorcontrib><creatorcontrib>Lecompte, Thomas</creatorcontrib><creatorcontrib>Lamblin, Géraldine</creatorcontrib><creatorcontrib>Talon, Laurie</creatorcontrib><creatorcontrib>Muti, Léon</creatorcontrib><creatorcontrib>Massoulier, Sylvie</creatorcontrib><creatorcontrib>Pereira, Bruno</creatorcontrib><creatorcontrib>Lebreton, Aurélien</creatorcontrib><creatorcontrib>Abergel, Armand</creatorcontrib><title>Intraindividual variability over time of thrombin generation in patients with cirrhosis</title><title>Journal of thrombosis and haemostasis</title><addtitle>J Thromb Haemost</addtitle><description>Patients with cirrhosis are at high risk of thrombotic events, including portal vein thrombosis and venous thromboembolism. In such patients, hypercoagulability is not detected by conventional coagulation tests, but only by the thrombin generation assay (TGA) that integrates the role of pro- and anticoagulant factors. However, TGA use to predict clinical events depends on thrombin generation variability over time.
The aim of this study was to compare TGA intraindividual variability over time in patients with cirrhosis and in healthy controls.
Blood samples were prospectively collected from 34 healthy controls and 52 patients with cirrhosis at week 0 (inclusion), 6, and 12. TGA was performed with the calibrated automated thrombogram method, tissue factor (5 pM), phospholipids, and with and without thrombomodulin (4 nM) or activated protein C (1 nM).
When TGA was performed with thrombomodulin, endogenous thrombin potential in patients with cirrhosis was higher compared with controls and increased with cirrhosis severity. Stability over time of all thrombin generation parameters was excellent in healthy controls, good in Child-Turcotte-Pugh (CTP)-A patients, and poor in CTP-B/C patients (severe cirrhosis). In CTP-B/C patients, the phenotype was more variable because one-third of patients switched to normal or hypercoagulability during the 3-month follow-up.
A study with longer monitoring is needed to correlate the hypercoagulable phenotype of patients with cirrhosis with the occurrence of thrombotic events.
•Thrombin generation could be a promising tool for predicting clinical events in cirrhosis.•It is essential to know thrombin generation intraindividual variability over time.•Stability over time was good in patients with mild cirrhosis and poor in severe.•Long-term monitoring is needed to correlate hypercoagulability with thrombotic events.</description><subject>Blood Coagulation Tests - methods</subject><subject>cirrhosis</subject><subject>Hematology</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>hypercoagulability</subject><subject>Life Sciences</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>monitoring</subject><subject>stability</subject><subject>thrombin</subject><subject>Thrombin - metabolism</subject><subject>Thrombomodulin</subject><subject>Thrombophilia</subject><subject>Thrombosis</subject><issn>1538-7836</issn><issn>1538-7933</issn><issn>1538-7836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAQQC0EoqXwBzggH-Gwwd9OJC5VBbTSShxA4mg58YTMKokX25uq_55EWypOnDwevXmHR8hbzirOuPl4qA5l8JVgQlZMVIyJZ-SSa1nvbC3N83_mC_Iq5wNjvNGCvSQX0lhdW2Euyc-7uSSPc8AFw8mPdPEJfYsjlgcaF0i04AQ09rQMKU4tzvQXzJB8wTjT9XdcJ5hLpvdYBtphSkPMmF-TF70fM7x5fK_I9y-ff9zc7vbfvt7dXO93nZKq7LyxTSs70UrbiMb4oLSXXoHR0AblbW1UHYI2PQ_QGql7XnuhTW1r1igjr8iHs3XwozsmnHx6cNGju73eu23HlNRSabXwlX1_Zo8p_j5BLm7C3ME4-hniKTthrTZcNPWmFWe0SzHnBP2TmzO3pXcHt6V3W3rHhFvTr0fvHv2ndoLwdPK39Qp8OgOw9lgQksvdmq6DgAm64kLE__n_AHpglSg</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Sinegre, Thomas</creator><creator>Duron, Cédric</creator><creator>Lecompte, Thomas</creator><creator>Lamblin, Géraldine</creator><creator>Talon, Laurie</creator><creator>Muti, Léon</creator><creator>Massoulier, Sylvie</creator><creator>Pereira, Bruno</creator><creator>Lebreton, Aurélien</creator><creator>Abergel, Armand</creator><general>Elsevier Inc</general><general>Wiley</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>1XC</scope><orcidid>https://orcid.org/0000-0001-7480-1052</orcidid></search><sort><creationdate>202306</creationdate><title>Intraindividual variability over time of thrombin generation in patients with cirrhosis</title><author>Sinegre, Thomas ; Duron, Cédric ; Lecompte, Thomas ; Lamblin, Géraldine ; Talon, Laurie ; Muti, Léon ; Massoulier, Sylvie ; Pereira, Bruno ; Lebreton, Aurélien ; Abergel, Armand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-a679b3c2b379296ad45a3a4e65ebd4a78648dd56f1deb635f18a25687809463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Blood Coagulation Tests - methods</topic><topic>cirrhosis</topic><topic>Hematology</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>hypercoagulability</topic><topic>Life Sciences</topic><topic>Liver Cirrhosis - complications</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>monitoring</topic><topic>stability</topic><topic>thrombin</topic><topic>Thrombin - metabolism</topic><topic>Thrombomodulin</topic><topic>Thrombophilia</topic><topic>Thrombosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sinegre, Thomas</creatorcontrib><creatorcontrib>Duron, Cédric</creatorcontrib><creatorcontrib>Lecompte, Thomas</creatorcontrib><creatorcontrib>Lamblin, Géraldine</creatorcontrib><creatorcontrib>Talon, Laurie</creatorcontrib><creatorcontrib>Muti, Léon</creatorcontrib><creatorcontrib>Massoulier, Sylvie</creatorcontrib><creatorcontrib>Pereira, Bruno</creatorcontrib><creatorcontrib>Lebreton, Aurélien</creatorcontrib><creatorcontrib>Abergel, Armand</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>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sinegre, Thomas</au><au>Duron, Cédric</au><au>Lecompte, Thomas</au><au>Lamblin, Géraldine</au><au>Talon, Laurie</au><au>Muti, Léon</au><au>Massoulier, Sylvie</au><au>Pereira, Bruno</au><au>Lebreton, Aurélien</au><au>Abergel, Armand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraindividual variability over time of thrombin generation in patients with cirrhosis</atitle><jtitle>Journal of thrombosis and haemostasis</jtitle><addtitle>J Thromb Haemost</addtitle><date>2023-06</date><risdate>2023</risdate><volume>21</volume><issue>6</issue><spage>1441</spage><epage>1452</epage><pages>1441-1452</pages><issn>1538-7836</issn><issn>1538-7933</issn><eissn>1538-7836</eissn><abstract>Patients with cirrhosis are at high risk of thrombotic events, including portal vein thrombosis and venous thromboembolism. In such patients, hypercoagulability is not detected by conventional coagulation tests, but only by the thrombin generation assay (TGA) that integrates the role of pro- and anticoagulant factors. However, TGA use to predict clinical events depends on thrombin generation variability over time.
The aim of this study was to compare TGA intraindividual variability over time in patients with cirrhosis and in healthy controls.
Blood samples were prospectively collected from 34 healthy controls and 52 patients with cirrhosis at week 0 (inclusion), 6, and 12. TGA was performed with the calibrated automated thrombogram method, tissue factor (5 pM), phospholipids, and with and without thrombomodulin (4 nM) or activated protein C (1 nM).
When TGA was performed with thrombomodulin, endogenous thrombin potential in patients with cirrhosis was higher compared with controls and increased with cirrhosis severity. Stability over time of all thrombin generation parameters was excellent in healthy controls, good in Child-Turcotte-Pugh (CTP)-A patients, and poor in CTP-B/C patients (severe cirrhosis). In CTP-B/C patients, the phenotype was more variable because one-third of patients switched to normal or hypercoagulability during the 3-month follow-up.
A study with longer monitoring is needed to correlate the hypercoagulable phenotype of patients with cirrhosis with the occurrence of thrombotic events.
•Thrombin generation could be a promising tool for predicting clinical events in cirrhosis.•It is essential to know thrombin generation intraindividual variability over time.•Stability over time was good in patients with mild cirrhosis and poor in severe.•Long-term monitoring is needed to correlate hypercoagulability with thrombotic events.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>36758726</pmid><doi>10.1016/j.jtha.2023.02.002</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7480-1052</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Blood Coagulation Tests - methods cirrhosis Hematology Human health and pathology Humans hypercoagulability Life Sciences Liver Cirrhosis - complications Liver Cirrhosis - diagnosis monitoring stability thrombin Thrombin - metabolism Thrombomodulin Thrombophilia Thrombosis |
title | Intraindividual variability over time of thrombin generation in patients with cirrhosis |
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