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

Li Li, Mark Roest, Yaqiu Sang, Jasper A Remijn, Rob Fijnheer, Karel Smit, Dana Huskens, Jun Wan, Bas de Laat, Joke Konings*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

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.

Original languageEnglish
Article number919495
Number of pages9
JournalFrontiers in Cardiovascular Medicine
Volume9
DOIs
Publication statusPublished - 27 Jun 2022

Keywords

  • blood cells
  • multiple myeloma
  • platelet function
  • thrombin generation
  • thrombosis
  • VENOUS THROMBOEMBOLISM
  • HYPERCOAGULABLE STATE
  • MONOCLONAL GAMMOPATHY
  • INCREASED RISK
  • PLASMA
  • ABNORMALITIES
  • COAGULATION
  • ACTIVATION
  • PLATELETS
  • CELLS

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