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Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process

Thrombin generation (TG) is known as a physiological approach to assess the hemostatic function. Although it correlates well with thrombosis and bleeding, in the current setup it is not sensitive to the effects of fluctuations in single coagulation factors. We optimized the calibrated automated thro...

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Autores principales: Bai, Cuicui, Konings, Joke, Ninivaggi, Marisa, Lancé, Marcus, de Laat, Bas, de Laat-Kremers, Romy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530111/
https://www.ncbi.nlm.nih.gov/pubmed/36204573
http://dx.doi.org/10.3389/fcvm.2022.1000812
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author Bai, Cuicui
Konings, Joke
Ninivaggi, Marisa
Lancé, Marcus
de Laat, Bas
de Laat-Kremers, Romy
author_facet Bai, Cuicui
Konings, Joke
Ninivaggi, Marisa
Lancé, Marcus
de Laat, Bas
de Laat-Kremers, Romy
author_sort Bai, Cuicui
collection PubMed
description Thrombin generation (TG) is known as a physiological approach to assess the hemostatic function. Although it correlates well with thrombosis and bleeding, in the current setup it is not sensitive to the effects of fluctuations in single coagulation factors. We optimized the calibrated automated thrombinography (CAT) method to quantify FII, FV and FX activity within the coagulation system. The CAT assay was fine-tuned for the assessment of FII, FV and FX by diluting the samples in FII-, FV-, or FX-deficient plasma, respectively, and measuring TG. Plasma FII levels correlated linearly with the ETP up to a plasma concentration of 100% FII. FV and FX levels correlated linearly with the peak height up to a plasma level of 2.5% FV and 10% FX, respectively. Sensitized CAT protocols were designed by adding a fixed volume of a pre-diluted patient sample to FII, FV, and FX deficient plasma in TG experiments. This approach makes the TG measurement dependent on the activity of the respective coagulation factor. The ETP or peak height were quantified as readouts for the coagulation factor activity. The intra- and inter-assay variation coefficients varied from 5.0 to 8.6%, and from 3.5 to 5.9%, respectively. Reference values were determined in 120 healthy subjects and the assays were clinically validated in 60 patients undergoing coronary artery bypass grafting (CABG). The sensitized CAT assays revealed that the contribution of FII, FV, and FX to the TG process was reduced after CABG surgery, leading to reduced prothrombin conversion and subsequently, lower TG.
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spelling pubmed-95301112022-10-05 Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process Bai, Cuicui Konings, Joke Ninivaggi, Marisa Lancé, Marcus de Laat, Bas de Laat-Kremers, Romy Front Cardiovasc Med Cardiovascular Medicine Thrombin generation (TG) is known as a physiological approach to assess the hemostatic function. Although it correlates well with thrombosis and bleeding, in the current setup it is not sensitive to the effects of fluctuations in single coagulation factors. We optimized the calibrated automated thrombinography (CAT) method to quantify FII, FV and FX activity within the coagulation system. The CAT assay was fine-tuned for the assessment of FII, FV and FX by diluting the samples in FII-, FV-, or FX-deficient plasma, respectively, and measuring TG. Plasma FII levels correlated linearly with the ETP up to a plasma concentration of 100% FII. FV and FX levels correlated linearly with the peak height up to a plasma level of 2.5% FV and 10% FX, respectively. Sensitized CAT protocols were designed by adding a fixed volume of a pre-diluted patient sample to FII, FV, and FX deficient plasma in TG experiments. This approach makes the TG measurement dependent on the activity of the respective coagulation factor. The ETP or peak height were quantified as readouts for the coagulation factor activity. The intra- and inter-assay variation coefficients varied from 5.0 to 8.6%, and from 3.5 to 5.9%, respectively. Reference values were determined in 120 healthy subjects and the assays were clinically validated in 60 patients undergoing coronary artery bypass grafting (CABG). The sensitized CAT assays revealed that the contribution of FII, FV, and FX to the TG process was reduced after CABG surgery, leading to reduced prothrombin conversion and subsequently, lower TG. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9530111/ /pubmed/36204573 http://dx.doi.org/10.3389/fcvm.2022.1000812 Text en Copyright © 2022 Bai, Konings, Ninivaggi, Lancé, de Laat and de Laat-Kremers. 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
Bai, Cuicui
Konings, Joke
Ninivaggi, Marisa
Lancé, Marcus
de Laat, Bas
de Laat-Kremers, Romy
Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title_full Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title_fullStr Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title_full_unstemmed Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title_short Assessing the individual roles of FII, FV, and FX activity in the thrombin generation process
title_sort assessing the individual roles of fii, fv, and fx activity in the thrombin generation process
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530111/
https://www.ncbi.nlm.nih.gov/pubmed/36204573
http://dx.doi.org/10.3389/fcvm.2022.1000812
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