Literature DB >> 25876231

Qualitative and quantitative modifications of von Willebrand factor in patients with essential thrombocythemia and controlled platelet count.

S Lancellotti1, A Dragani2, P Ranalli2, G Petrucci3, M Basso1, R Tartaglione4, B Rocca3, R De Cristofaro1.   

Abstract

BACKGROUND: Essential thrombocythemia (ET) is characterized by increased platelets and prevalent thrombosis. An acquired von Willebrand factor (VWF) disease has been hypothesized and inconsistently associated with extreme thrombocytosis or rare bleeding in ET. Whether VWF is modified in ET patients with controlled platelet count remains unclear.
OBJECTIVES: We studied different VWF- and platelet-associated parameters in ET patients treated according to current recommendations. PATIENTS/
METHODS: Sixty-nine ET patients (M = 29; median age, 62 [48-70] years; platelets, 432 [337-620] × 10(3)  μL(-1) ), 69 matched controls and 10 subjects with reactive thrombocytosis (RT) were studied. VWF:antigen (Ag), activity (act), electrophoretic patterns, VWF:propeptide, plasma glycocalycin (GC), glycoproteinV (GpV), ADAMTS-13, elastase, C-reactive protein and serum thromboxane (TX)B2 were measured.
RESULTS: In ET patients, VWF:Ag was increased by 31 ± 13% vs. controls (P < 0.01), without dependence of blood groups, while VWF:act was reduced by 21 ± 12% vs. controls and by 50 ± 24% vs. RT (P < 0.01). The VWF:act/VWF:Ag ratios in ET were reduced by 35 ± 17% vs. controls and RT patients (P < 0.001) and significantly associated with: immature or total platelet counts, GC, GpV and TXB2 . In multivariable analysis, only GC inversely predicted ET patients' VWF:act/VWF:Ag ratios (β = -0.42, P = 0.01). By electrophoresis analyses, high-molecular-weight VWF multimers were variably reduced with atypical cleavage bands in ET only. VWF:propeptide, ADAMTS-13 and elastase levels were normal in ET patients. Platelet-associated ADAM-10 and ADAM-17 hydrolyzed VWFm in vitro, showing patterns similar to those in ET samples.
CONCLUSIONS: In ET patients with controlled platelet counts, the VWF:act/VWF:Ag ratio is decreased and predicted by GC, a product of platelet activation. ADAM-10 and/or ADAM-17 might be involved. In vivo platelet activation, which characterizes ET, might contribute to disease-specific VWF alterations.
© 2015 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  ADAMTS13 protein, human; essential thrombocythemia; glycocalicin; platelet membrane glycoprotein V; von Willebrand factor

Mesh:

Substances:

Year:  2015        PMID: 25876231     DOI: 10.1111/jth.12967

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  11 in total

1.  The course of acquired von Willebrand syndrome during pregnancy among patients with essential thrombocytosis.

Authors:  Amihai Rottenstreich; Geffen Kleinstern; Hagai Amsalem; Yosef Kalish
Journal:  J Thromb Thrombolysis       Date:  2018-10       Impact factor: 2.300

Review 2.  Low-risk polycythemia vera and essential thrombocythemia: management considerations and future directions.

Authors:  Hannah Goulart; John Mascarenhas; Douglas Tremblay
Journal:  Ann Hematol       Date:  2022-03-28       Impact factor: 3.673

3.  Presence of portal vein thrombosis in liver cirrhosis is strongly associated with low levels of ADAMTS-13: a pilot study.

Authors:  Stefano Lancellotti; Maria Basso; Vito Veca; Monica Sacco; Laura Riccardi; Maurizio Pompili; Raimondo De Cristofaro
Journal:  Intern Emerg Med       Date:  2016-05-24       Impact factor: 3.397

4.  Extreme Levels of Platelet Count in Essential Thrombocythemia: Management and Outcome, Report of Two Cases.

Authors:  Mohammad Abu-Tineh; Mohamed A Yassin
Journal:  Case Rep Oncol       Date:  2020-06-04

Review 5.  Prefibrotic myelofibrosis: treatment algorithm 2018.

Authors:  Guido Finazzi; Alessandro M Vannucchi; Tiziano Barbui
Journal:  Blood Cancer J       Date:  2018-11-07       Impact factor: 11.037

6.  Ruxolitinib for the Treatment of Essential Thrombocythemia.

Authors:  Arief Gunawan; Patrick Harrington; Natalia Garcia-Curto; Donal McLornan; Deepti Radia; Claire Harrison
Journal:  Hemasphere       Date:  2018-06-12

7.  Thrombocytosis with acquired von Willebrand disease in an adolescent with sickle cell disease.

Authors:  Marianne E M Yee; Glaivy Batsuli; Satheesh Chonat; Sunita Park
Journal:  Clin Case Rep       Date:  2020-11-20

8.  Practice patterns and outcomes of direct oral anticoagulant use in myeloproliferative neoplasm patients.

Authors:  Joan How; Charlotte Story; Siyang Ren; Donna Neuberg; Rachel P Rosovsky; Gabriela S Hobbs; Jean M Connors
Journal:  Blood Cancer J       Date:  2021-11-05       Impact factor: 11.037

Review 9.  Role of fluid shear stress in regulating VWF structure, function and related blood disorders.

Authors:  Shobhit Gogia; Sriram Neelamegham
Journal:  Biorheology       Date:  2015       Impact factor: 1.875

10.  Increased von Willebrand factor levels in polycythemia vera and phenotypic differences with essential thrombocythemia.

Authors:  Monica Sacco; Paola Ranalli; Stefano Lancellotti; Giovanna Petrucci; Alfredo Dragani; Bianca Rocca; Raimondo De Cristofaro
Journal:  Res Pract Thromb Haemost       Date:  2020-02-28
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.