Ayer Mesut, Menken İlhan, Yamak Mehmet, Ayer Fatma Aylin, Kırkızlar Onur, Burak Aktuğlu M
Department of Hematology, Haseki Training and Research Hospital, Millet Cd., Aksaray/Fatih, 34087 Istanbul, Turkey.
Department of Internal Medicine, Haseki Training and Research Hospital, Istanbul, Turkey.
Indian J Hematol Blood Transfus. 2017 Jun;33(2):181-187. doi: 10.1007/s12288-016-0685-8. Epub 2016 May 24.
Thrombosis and bleeding are the main complications of chronic myeloproliferative diseases. Mean platelet volume (MPV) is an important indicator of the platelet activation. The aim of the present study was to assess the interrelationships between MPV, JAK-2 gene mutation and thromboembolic events in patients with ET and PV. Patients with ET (n = 60) and PV (n = 46) were compared to the secondary erythrocytosis group (n = 19); and a control group of age and sex matched healthy volunteers (n = 52). Besides demographic, clinical and laboratory data; thrombotic and hemorrhagic events were recorded for each patient. Platelet counts, MPV and JAK2 mutations were studied; and their relation with thromboembolic events were investigated using SPSS program for statistical analysis. There was no significant difference between groups regarding age ( = 0.188). Mean platelet count was significantly higher in ET group than other groups ( < 0.0001). Mean platelet count in PV group was significantly higher than control ( < 0.0001) and secondary erythrocytosis groups ( < 0.0001). In the ET group, MPV values were significantly lower than the control group and PV group. In the ET group, those with thromboembolia had lower platelet counts. There was no relation between MPV and thromboembolic event rate in PV, ET and secondary erithrocytosis groups; while no event was recorded in the control group. There was no relation between thromboembolic event rate and JAK 2 mutation. The association of JAK-2 mutation and high MPV especially in ET and PV groups does not contribute to the thromboembolic events.
血栓形成和出血是慢性骨髓增殖性疾病的主要并发症。平均血小板体积(MPV)是血小板活化的重要指标。本研究旨在评估原发性血小板增多症(ET)和真性红细胞增多症(PV)患者中MPV、JAK-2基因突变与血栓栓塞事件之间的相互关系。将ET患者(n = 60)和PV患者(n = 46)与继发性红细胞增多症组(n = 19)进行比较;并与年龄和性别匹配的健康志愿者对照组(n = 52)进行比较。除了人口统计学、临床和实验室数据外;还记录了每位患者的血栓形成和出血事件。研究了血小板计数、MPV和JAK2基因突变;并使用SPSS程序进行统计分析,研究它们与血栓栓塞事件的关系。各组之间在年龄方面无显著差异(P = 0.188)。ET组的平均血小板计数显著高于其他组(P < 0.0001)。PV组的平均血小板计数显著高于对照组(P < 0.0001)和继发性红细胞增多症组(P < 0.0001)。在ET组中,MPV值显著低于对照组和PV组。在ET组中,发生血栓栓塞的患者血小板计数较低。在PV、ET和继发性红细胞增多症组中,MPV与血栓栓塞事件发生率之间无关联;而对照组未记录到事件。血栓栓塞事件发生率与JAK 2基因突变之间无关联。JAK-2基因突变与高MPV的关联,尤其是在ET和PV组中,与血栓栓塞事件无关。