2019
High level of circulat ing microparticles in patients with BCR/ ABL negative myeloproliferative neoplasm - A pilot study
ASWAD, Mohamed Hussam, Jarmila KISSOVÁ, Lucie ŘÍHOVÁ, Jiřina ZAVŘELOVÁ, Petra OVESNÁ et. al.Základní údaje
Originální název
High level of circulat ing microparticles in patients with BCR/ ABL negative myeloproliferative neoplasm - A pilot study
Autoři
ASWAD, Mohamed Hussam (760 Sýrie, garant, domácí), Jarmila KISSOVÁ (203 Česká republika, domácí), Lucie ŘÍHOVÁ (203 Česká republika, domácí), Jiřina ZAVŘELOVÁ (203 Česká republika, domácí), Petra OVESNÁ (203 Česká republika, domácí) a Miroslav PENKA (203 Česká republika, domácí)
Vydání
Klinická onkologie, Brno, Ambit Media a.s. 2019, 0862-495X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Kód RIV
RIV/00216224:14110/19:00112977
Organizační jednotka
Lékařská fakulta
Klíčová slova anglicky
Janus Kinase 2; microparticles; myeloproliferative disorders; procoagulation activity; thrombosis
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 18. 2. 2020 07:49, Mgr. Tereza Miškechová
Anotace
V originále
BACKGROUND: Microparticles (MPs) are small (0.1-1 [MU]m) cell-derived vesicles released during activation or apoptosis, with a surface-exposed phosphatidylserine along with antigens indicating the cellular origin. The level of MPs is known to be elevated in thromboembolic diseases and malignancies; it is believed that MPs are not only amplifying but can also initiate the thrombogenesis processes. BCR/ABL negative myeloproliferative neoplasms (MPNs) are clonal haematopoietic diseases, which include polycythemia vera, essential thrombocythemia and primary myelofibrosis. One of the main problems of MPN patients is high risk and incidence of thrombosis which affect the survival, quality of life and life expectancy. PATIENTS AND METHODS: The clinical significance of circulating MPs was assessed in a group of 179 patients with BCR/ABL-negative MPNs. Analysis of MPs was done using flow cytometry on 417 samples, and MPs procoagulation activity was performed using a functional assay called Zymuphen MP-activity (Hyphen Biomed, Neuville-sur-oise, France) on 274 samples. RESULTS: Significantly higher absolute and relative count of platelet MPs was found in MPN patients when compared with healthy group, respectively (p = 0.001, p = 0.043). Erythrocyte MPs were also significantly higher in MPN patients than in the healthy group (p < 0.001). Procoagulation activity of MPs was as well significantly higher in patients compared to the control group (p < 0.001). Patients with primary myelofibrosis had decreased absolute and relative count of platelet MPs compared to polycythemia vera and essential thrombocythemia patients, respectively (p = 0.008, p = 0.014). Presence of JAK2V617F mutation was associated with higher absolute and relative count of platelet MPs, respectively (p = 0.045, p = 0.029). CONCLUSION: Although some literature data support the hypothesis of a direct relation between MPs and thrombotic events in MPN patients, further studies are needed to evaluate the clinical implication of MPs in the hypercoagulation state of MPN patients.
Návaznosti
MUNI/A/1105/2018, interní kód MU |
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