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Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay

BACKGROUND: The haemostatic balance is an equilibrium of pro- and anticoagulant factors that work synergistically to prevent bleeding and thrombosis. As thrombin is the central enzyme in the coagulation pathway, it is desirable to measure thrombin generation (TG) in order to detect possible bleeding...

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Autores principales: Carlo, Audrey, Yan, Qiuting, Ten Cate, Hugo, De Laat-Kremers, Romy, De Laat, Bas, Ninivaggi, Marisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360406/
https://www.ncbi.nlm.nih.gov/pubmed/35958413
http://dx.doi.org/10.3389/fcvm.2022.912433
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author Carlo, Audrey
Yan, Qiuting
Ten Cate, Hugo
De Laat-Kremers, Romy
De Laat, Bas
Ninivaggi, Marisa
author_facet Carlo, Audrey
Yan, Qiuting
Ten Cate, Hugo
De Laat-Kremers, Romy
De Laat, Bas
Ninivaggi, Marisa
author_sort Carlo, Audrey
collection PubMed
description BACKGROUND: The haemostatic balance is an equilibrium of pro- and anticoagulant factors that work synergistically to prevent bleeding and thrombosis. As thrombin is the central enzyme in the coagulation pathway, it is desirable to measure thrombin generation (TG) in order to detect possible bleeding or thrombotic phenotypes, as well as to investigate the capacity of drugs affecting the formation of thrombin. By investigating the underlying processes of TG (i.e., prothrombin conversion and inactivation), additional information is collected about the dynamics of thrombin formation. OBJECTIVES: To obtain reference values for thrombin dynamics (TD) analysis in 112 healthy donors using an automated system for TG. METHODS: TG was measured on the ST Genesia, fibrinogen on the Start, anti-thrombin (AT) on the STA R Max and α(2)Macroglobulin (α(2)M) with an in-house chromogenic assay. RESULTS: TG was measured using STG-BleedScreen, STG-ThromboScreen and STG-DrugScreen. The TG data was used as an input for TD analysis, in combination with plasma levels of AT, α(2)M and fibrinogen that were 113% (108–118%), 2.6 μM (2.2 μM−3.1 μM) and 2.9 g/L (2.6–3.2 g/L), respectively. The maximum rate of the prothrombinase complex (PCmax) and the total amount of prothrombin converted (PCtot) increased with increasing tissue factor (TF) concentration. PC(tot) increased from 902 to 988 nM, whereas PC(max) increased from 172 to 508 nM/min. Thrombin (T)-AT and T-α(2)M complexes also increased with increasing TF concentration (i.e., from 860 to 955 nM and from 28 to 33 nm, respectively). PC(tot), T-AT and T-α(2)M complex formation were strongly inhibited by addition of thrombomodulin (−44%, −43%, and −48%, respectively), whereas PC(max) was affected less (−24%). PC(tot), PC(max), T-AT, and T-α(2)M were higher in women using oral contraceptives (OC) compared to men/women without OC, and inhibition by thrombomodulin was also significantly less in women on OC (p < 0.05). CONCLUSIONS: TG measured on the ST Genesia can be used as an input for TD analysis. The data obtained can be used as reference values for future clinical studies as the balance between prothrombin conversion and thrombin inactivation has shown to be useful in several clinical settings.
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spelling pubmed-93604062022-08-10 Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay Carlo, Audrey Yan, Qiuting Ten Cate, Hugo De Laat-Kremers, Romy De Laat, Bas Ninivaggi, Marisa Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: The haemostatic balance is an equilibrium of pro- and anticoagulant factors that work synergistically to prevent bleeding and thrombosis. As thrombin is the central enzyme in the coagulation pathway, it is desirable to measure thrombin generation (TG) in order to detect possible bleeding or thrombotic phenotypes, as well as to investigate the capacity of drugs affecting the formation of thrombin. By investigating the underlying processes of TG (i.e., prothrombin conversion and inactivation), additional information is collected about the dynamics of thrombin formation. OBJECTIVES: To obtain reference values for thrombin dynamics (TD) analysis in 112 healthy donors using an automated system for TG. METHODS: TG was measured on the ST Genesia, fibrinogen on the Start, anti-thrombin (AT) on the STA R Max and α(2)Macroglobulin (α(2)M) with an in-house chromogenic assay. RESULTS: TG was measured using STG-BleedScreen, STG-ThromboScreen and STG-DrugScreen. The TG data was used as an input for TD analysis, in combination with plasma levels of AT, α(2)M and fibrinogen that were 113% (108–118%), 2.6 μM (2.2 μM−3.1 μM) and 2.9 g/L (2.6–3.2 g/L), respectively. The maximum rate of the prothrombinase complex (PCmax) and the total amount of prothrombin converted (PCtot) increased with increasing tissue factor (TF) concentration. PC(tot) increased from 902 to 988 nM, whereas PC(max) increased from 172 to 508 nM/min. Thrombin (T)-AT and T-α(2)M complexes also increased with increasing TF concentration (i.e., from 860 to 955 nM and from 28 to 33 nm, respectively). PC(tot), T-AT and T-α(2)M complex formation were strongly inhibited by addition of thrombomodulin (−44%, −43%, and −48%, respectively), whereas PC(max) was affected less (−24%). PC(tot), PC(max), T-AT, and T-α(2)M were higher in women using oral contraceptives (OC) compared to men/women without OC, and inhibition by thrombomodulin was also significantly less in women on OC (p < 0.05). CONCLUSIONS: TG measured on the ST Genesia can be used as an input for TD analysis. The data obtained can be used as reference values for future clinical studies as the balance between prothrombin conversion and thrombin inactivation has shown to be useful in several clinical settings. Frontiers Media S.A. 2022-07-26 /pmc/articles/PMC9360406/ /pubmed/35958413 http://dx.doi.org/10.3389/fcvm.2022.912433 Text en Copyright © 2022 Carlo, Yan, Ten Cate, De Laat-Kremers, De Laat and Ninivaggi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Carlo, Audrey
Yan, Qiuting
Ten Cate, Hugo
De Laat-Kremers, Romy
De Laat, Bas
Ninivaggi, Marisa
Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title_full Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title_fullStr Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title_full_unstemmed Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title_short Semi-automated thrombin dynamics applying the ST Genesia thrombin generation assay
title_sort semi-automated thrombin dynamics applying the st genesia thrombin generation assay
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360406/
https://www.ncbi.nlm.nih.gov/pubmed/35958413
http://dx.doi.org/10.3389/fcvm.2022.912433
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