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Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile

BACKGROUND: Multiple myeloma (MM) is associated with a high prevalence of bleeding and an increased risk of thrombo-embolism. MM patients have reduced platelet- and red blood cell (RBC) numbers in blood, which may indicate that the paradoxical hemostasis profile is a consequence of a disturbed plate...

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Autores principales: Li, Li, Roest, Mark, Sang, Yaqiu, Remijn, Jasper A., Fijnheer, Rob, Smit, Karel, Huskens, Dana, Wan, Jun, de Laat, Bas, Konings, Joke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271700/
https://www.ncbi.nlm.nih.gov/pubmed/35833182
http://dx.doi.org/10.3389/fcvm.2022.919495
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author Li, Li
Roest, Mark
Sang, Yaqiu
Remijn, Jasper A.
Fijnheer, Rob
Smit, Karel
Huskens, Dana
Wan, Jun
de Laat, Bas
Konings, Joke
author_facet Li, Li
Roest, Mark
Sang, Yaqiu
Remijn, Jasper A.
Fijnheer, Rob
Smit, Karel
Huskens, Dana
Wan, Jun
de Laat, Bas
Konings, Joke
author_sort Li, Li
collection PubMed
description BACKGROUND: Multiple myeloma (MM) is associated with a high prevalence of bleeding and an increased risk of thrombo-embolism. MM patients have reduced platelet- and red blood cell (RBC) numbers in blood, which may indicate that the paradoxical hemostasis profile is a consequence of a disturbed platelet and RBC homeostasis. OBJECTIVES: To get better insight in the disbalanced hemostasis of MM patients. METHODS: We conducted a case-control study on the whole blood (WB) coagulation profiles of 21 MM patients and 21 controls. We measured thrombin generation (TG) in WB and platelet poor plasma (PPP) of MM patients and controls. RESULTS: In WB-TG, we observed that the median time to the thrombin Peak was 52% longer in MM patients than in controls, while the median endogenous thrombin potential until the Peak (ETPp) was 39% higher in MM-patients than in controls. In line with these findings, the levels of platelets, RBCs, white blood cells and agonist induced platelet activation were decreased in MM patients compared to controls. The plasma TG experiments showed no differences between MM-patients and controls. CONCLUSION: Patients with MM have a disturbed blood cell metabolism and a disbalanced WB-TG profile. This disbalance may explain the paradoxically high prevalence of bleeding symptoms in MM patients vs. an increased thrombosis risk. There was no disturbance observed in plasma TG, indicating that blood cells are the major determinants for the disbalanced hemostasis in MM patients.
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spelling pubmed-92717002022-07-12 Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile Li, Li Roest, Mark Sang, Yaqiu Remijn, Jasper A. Fijnheer, Rob Smit, Karel Huskens, Dana Wan, Jun de Laat, Bas Konings, Joke Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Multiple myeloma (MM) is associated with a high prevalence of bleeding and an increased risk of thrombo-embolism. MM patients have reduced platelet- and red blood cell (RBC) numbers in blood, which may indicate that the paradoxical hemostasis profile is a consequence of a disturbed platelet and RBC homeostasis. OBJECTIVES: To get better insight in the disbalanced hemostasis of MM patients. METHODS: We conducted a case-control study on the whole blood (WB) coagulation profiles of 21 MM patients and 21 controls. We measured thrombin generation (TG) in WB and platelet poor plasma (PPP) of MM patients and controls. RESULTS: In WB-TG, we observed that the median time to the thrombin Peak was 52% longer in MM patients than in controls, while the median endogenous thrombin potential until the Peak (ETPp) was 39% higher in MM-patients than in controls. In line with these findings, the levels of platelets, RBCs, white blood cells and agonist induced platelet activation were decreased in MM patients compared to controls. The plasma TG experiments showed no differences between MM-patients and controls. CONCLUSION: Patients with MM have a disturbed blood cell metabolism and a disbalanced WB-TG profile. This disbalance may explain the paradoxically high prevalence of bleeding symptoms in MM patients vs. an increased thrombosis risk. There was no disturbance observed in plasma TG, indicating that blood cells are the major determinants for the disbalanced hemostasis in MM patients. Frontiers Media S.A. 2022-06-27 /pmc/articles/PMC9271700/ /pubmed/35833182 http://dx.doi.org/10.3389/fcvm.2022.919495 Text en Copyright © 2022 Li, Roest, Sang, Remijn, Fijnheer, Smit, Huskens, Wan, de Laat and Konings. 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
Li, Li
Roest, Mark
Sang, Yaqiu
Remijn, Jasper A.
Fijnheer, Rob
Smit, Karel
Huskens, Dana
Wan, Jun
de Laat, Bas
Konings, Joke
Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title_full Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title_fullStr Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title_full_unstemmed Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title_short Patients With Multiple Myeloma Have a Disbalanced Whole Blood Thrombin Generation Profile
title_sort patients with multiple myeloma have a disbalanced whole blood thrombin generation profile
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271700/
https://www.ncbi.nlm.nih.gov/pubmed/35833182
http://dx.doi.org/10.3389/fcvm.2022.919495
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