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DOI 10.1016/j.thromres.2024.01.018

Медицинская библиотека · Thrombosis research · 2024

Activated protein C and free protein S in patients with mild to moderate bleeding disorders.

Mehic Dino, Schramm Theresa, Forstner-Bergauer Birgit, Haslacher Helmuth, Ay Cihan, Pabinger Ingrid, Gebhart Johanna

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Аннотация

BACKGROUND

Underlying mechanisms for bleeding and impaired thrombin generation (TG) and plasma clot formation (PCF) in patients with mild to moderate bleeding disorders (MBDs) are still to be elucidated, especially in bleeding disorder of unknown cause (BDUC). The role of the natural anticoagulants activated protein C (APC) and free protein S (PS) has not yet been investigated in this patient population.

AIMS: To analyze antigen levels of APC and PS in patients with MBDs and BDUC and investigate associations to clinical bleeding phenotype and severity as well as and hemostatic capacity.

METHODS

Antigen levels of APC and free PS were measured in 262 patients from the Vienna Bleeding Biobank (VIBB), a single-center cohort study, by ELISA and compared to 61 healthy controls (HC).

RESULTS

Antigen levels of APC were higher in MBD patients than in HC when adjusted for age, sex and BMI (median (IQR) 33.1 (20.6-52.6) and 28.6 (16.4-47.2) ng/mL). This was most pronounced in patients with BDUC (35.3 (21.7-54.3) ng/mL). No differences in PS antigen levels between patients and HC were seen overall, or according to specific diagnoses. Further, no association between APC or PS and bleeding severity or global tests of hemostasis or TG were identified, while paradoxically APC weakly correlated with shorter lag time and time to peak of PCF in BDUC.

CONCLUSION

Our data demonstrate increased antigen levels of APC in BDUC, which might contribute to the bleeding tendency in some patients and could be a future therapeutic target in BDUC.

Для цитирования: Mehic Dino, Schramm Theresa, Forstner-Bergauer Birgit, Haslacher Helmuth, Ay Cihan, Pabinger Ingrid, Gebhart Johanna. Activated protein C and free protein S in patients with mild to moderate bleeding disorders.. Thrombosis research. 2024. DOI: 10.1016/j.thromres.2024.01.018.

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