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首页> 外文期刊>Hematology >Relationship between JAK2V617F mutation, allele burden and coagulation function in Ph-negative myeloproliferative neoplasms
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Relationship between JAK2V617F mutation, allele burden and coagulation function in Ph-negative myeloproliferative neoplasms

机译:Ph阴性骨髓增生性肿瘤中JAK2V617F突变,等位基因负荷与凝血功能之间的关系

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Objectives: Our aim was to explore the relationship between JAK2V617F mutation allele burden and hematological parameters especially in coagulation function in Chinese population. Methods: This study included 133 Ph-negative myeloproliferative neoplasms (MPNs) patients between 2013 and 2016. All the clinical and experimental data of patients were collected at the time of the diagnosis without any prior treatment, including blood parameters, coagulation function, splenomegaly, vascular events and chromosome karyotype. PCR and qPCR were used to detect JAK2V617F mutation and JAK2V617F mutation allele burden. Results: In polycythemia vera patients, a positive correlation between the allele burden of JAK2V617F mutation and PLT counts was found; in essential thrombocythemia (ET) patients, WBC counts, RBC counts, HB, and HCT were higher in mutated patients than in wild-type patients. Furthermore, PT-INR was higher in ET and PMF mutated patients. In addition, a positive correlation between the allele burden of JAK2V617F mutation and activated partial thromboplastin time (APTT) was observed in JAK2V617F mutated ET patients. Conclusions: Higher hematologic parameters including counts of WBC, RBC, and PLT are closely associated with JAK2V617F mutation and its burden in Ph-negative MPNs; importantly, PT-INR, APTT are also related to JAK2V617F mutation and allele burden. Thus, our data indicate that JAK2V617F mutation allele burden might not only represent the burden of MPN but also alter the coagulation function.
机译:目的:我们的目的是探讨JAK2V617F突变等位基因负荷与血液学参数之间的关系,尤其是在中国人群的凝血功能方面。方法:本研究纳入2013年至2016年间133例Ph阴性的骨髓增生性肿瘤(MPNs)患者。在诊断时未进行任何事先治疗就收集了患者的所有临床和实验数据,包括血液参数,凝血功能,脾肿大,血管事件和染色体核型。 PCR和qPCR用于检测JAK2V617F突变和JAK2V617F突变等位基因负担。结果:真性红细胞增多症患者中,JAK2V617F突变的等位基因负担与PLT计数之间呈正相关;在原发性血小板增多症(ET)患者中,突变患者的WBC计数,RBC计数,HB和HCT高于野生型患者。此外,在ET和PMF突变的患者中PT-INR较高。此外,在JAK2V617F突变的ET患者中,JAK2V617F突变的等位基因负担与活化的部分凝血活酶时间(APTT)之间存在正相关。结论:较高的血液学参数(包括WBC,RBC和PLT计数)与JAK2V617F突变及其在Ph阴性MPN中的负担密切相关;重要的是,PT-INR,APTT也与JAK2V617F突变和等位基因负荷有关。因此,我们的数据表明,JAK2V617F突变等位基因负担可能不仅代表了MPN的负担,而且还改变了凝血功能。

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