• Thrombomodulin-induced inhibition of endogenous thrombin potential lower than 20% (R-ETP/TM) is common in patients with unprovoked VTE

  • Identifiable risk factors for R-ETP/TM have insufficient predicting performances and require further investigations.

Poorly controlled thrombin generation (TG) can induce venous thromboembolism (VTE). Assessing the global coagulation potential may help to characterize the risk of VTE. TG assay (TGA) quantifying the endogenous thrombin potential (ETP) and its inhibition after adding purified thrombomodulin (TM) allows certain thrombotic phenotypes to be recognized. We tested the TM-induced ETP variation in 989 uncoagulated patients with their first unprovoked VTE and 200 controls using an automated TGA and commercially available reagents. We found evidence of ETP resistance to TM, defined at the 5th percentile value found in Controls, in 406 patients (41.1%, p<0.0001), mixing tests in antiphospholipid antibody-negative patients showing no inhibitory activity. We investigated the 422 patients with full clinical and laboratory information for predictors of ETP resistance to TM (R-ETP/TM), found positive in 163 of them (38.6%). Multivariate analysis showed that D-dimers were positive, protein S and Rosner index were negative risk factors for R-ETP/TM (quantitative model), high D-dimers and FVIII, protein C < 65 I.U. and protein S < 50 I.U. were risk factors (qualitative model). The scores derived had insufficient predictive performances to diagnose R-ETP/TM, which is a frequent plasma phenotype in unprovoked VTE patients. The complete identification of its determinants deserves further investigations.

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Author notes

Data Sharing Statement:

Original data are available on request from the corresponding author, Jean-Christophe Gris (jean.christophe.gris@chu-nimes.fr). The de-identified individual participant data underlying the results reported will be available 3 months after publication and for up to 5 years after the publication date.

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First page of High incidence of thrombin generation resistance to thrombomodulin in patients with unprovoked venous thromboembolism.