Singh Kanwaljeet, Sazawal Sudha, Chhikara Sunita, Mahapatra Manoranjan, Saxena Renu
Department of Hematology, All India Institute of Medical Sciences, New Delhi, India.
Indian J Pathol Microbiol. 2018 Jul-Sep;61(3):371-374. doi: 10.4103/IJPM.IJPM_781_17.
: It is still a matter of debate regarding the association of JAK2V617F mutation with thrombosis in BCR-ABL negative CMPN patients. The role of JAK2V617F mutation in increasing the thrombotic risk in CMPNs is yet unequivocal.
: To clarify the contribution of JAK2V617F mutation in thrombosis in CMPN patients.
This retrospective study was done to evaluate role of JAK2V617F mutation in thrombosis in CMPNs.
65 CMPN patients (PV, ET and PMF) were analyzed for JAK2V617F mutation using ARMS-PCR and detailed history of thrombosis was recorded in these patients.
P values were 2 tailed, and statistical significance was set at P < 0.05.
: 46/65 were males and 19/65 were females [M: F: 2.4:1] with median age 46 years [range, 14-80 years]. Patients had median Hb 15.6 g/dl [range, 5.1-20.3], median TLC 10.7 × 10/l [range 2.4-216] and platelet count 360 × 10/l [range, 20-1859]. 32 were JAK2V617F positive and 33 were negative for this mutation. On comparing the prevalence of thrombosis in JAK2V617F positive patients with JAK2V617F negative patients, we observed that 20/32 (62.5%) JAK2V617F positive patients had thrombosis as compared to 16/33 (48%) in JAK2V617F negative patients (P = 0.04). We observed significant association of JAK2V617F mutation with thrombosis, however no association of this mutation with thrombosis was observed among the JAK2V617F negative patients.
Our study suggests that JAK2V617F mutation may increase the risk of thrombosis in CMPNs. This finding could lead to risk stratification, setting up the treatment strategy in CMPNs.
JAK2V617F突变与BCR-ABL阴性慢性髓性增殖性肿瘤(CMPN)患者血栓形成之间的关联仍存在争议。JAK2V617F突变在增加CMPNs患者血栓形成风险中的作用尚不明确。
阐明JAK2V617F突变在CMPN患者血栓形成中的作用。
本回顾性研究旨在评估JAK2V617F突变在CMPNs患者血栓形成中的作用。
采用ARMS-PCR对65例CMPN患者(真性红细胞增多症、原发性血小板增多症和原发性骨髓纤维化)进行JAK2V617F突变分析,并记录这些患者详细的血栓形成病史。
P值采用双侧检验,设定统计学显著性为P < 0.05。
65例患者中,46例为男性,19例为女性[男:女 = 2.4:1],中位年龄46岁[范围14 - 80岁]。患者的血红蛋白(Hb)中位数为15.6 g/dl[范围5.1 - 20.3],白细胞计数(TLC)中位数为10.7×10⁹/L[范围2.4 - 216],血小板计数为360×10⁹/L[范围20 - 1859]。32例患者JAK2V617F突变阳性,33例为阴性。比较JAK2V617F阳性患者与JAK2V617F阴性患者的血栓形成患病率发现,JAK2V617F阳性患者中有20/32(62.5%)发生血栓,而JAK2V617F阴性患者中有16/33(48%)发生血栓(P = 0.)。我们观察到JAK2V617F突变与血栓形成之间存在显著关联,然而在JAK2V617F阴性患者中未观察到该突变与血栓形成有关联。
我们的研究表明,JAK2V617F突变可能增加CMPNs患者的血栓形成风险。这一发现可能有助于进行风险分层,并制定CMPNs的治疗策略。