Positive-DAT and autoimmune manifestations in patients with JAK2V617F mutation

R. Akoum, Rita Chidiac, Joseph Yammine, M. Saade, E. Brihi
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Abstract

Objective: Myeloproliferative neoplasms (MPN) are occasionally associated with autoimmune manifestations. The prevalence of positive direct antiglobulin test (DAT) in patients with JAK2V617F mutation is not yet known. Methods: We conducted a cohort study of all consecutive patients with JAK2V617F mutation who underwent DAT at presentation from 2010 to 2022. We also looked for the prevalence of autoimmune diseases (AIDs) and relation to thrombosis. Results: Fifty nine patients formed the cohort, 22 females and 37 males, with a mean age of 65 years. The median follow-up time was 90 months. A positive-DAT was found in 6 to 7% of essential thrombocythemia (ET) and polycythemia vera (PV) patients, 60% of primary myelofibrosis (PMF) patients and 50% of myelodysplasia/myeloproliferation (MDS/MPN) patients with or without anemia. Autoimmune manifestations were present in 13% of patients with PV and 50% of those with MDS/MPN features. Overall, 25% of patients had autoimmune phenomena including the 15% with positive-DAT. Conclusion: In patients with JAK2V617F mutation, those with PMF and MDS/MPN subtypes are most likely to display a positive-DAT results and autoimmune manifestations (≥ 50%). Patients with PV and ET are less likely to exhibit autoimmune manifestations (≤ 10%). No correlation with the occurrence of thrombosis was seen.
JAK2V617F突变患者的DAT阳性和自身免疫表现
目的:骨髓增生性肿瘤(MPN)偶尔会伴有自身免疫表现。JAK2V617F突变患者中直接抗球蛋白试验(DAT)阳性的发生率尚不清楚。 研究方法我们对2010年至2022年期间所有在发病时接受DAT检测的连续JAK2V617F突变患者进行了一项队列研究。我们还调查了自身免疫性疾病(AID)的发病率以及与血栓形成的关系。 结果队列中有59名患者,其中女性22名,男性37名,平均年龄65岁。随访时间中位数为 90 个月。6%至7%的原发性血小板增多症(ET)和真性红细胞增多症(PV)患者、60%的原发性骨髓纤维化(PMF)患者和50%的骨髓增生异常/骨髓增生症(MDS/MPN)患者伴有或不伴有贫血,均发现DAT阳性。13%的骨髓纤维化患者和50%具有MDS/MPN特征的患者存在自身免疫表现。总体而言,25%的患者有自身免疫现象,其中包括15%的DAT阳性患者。 结论在JAK2V617F突变患者中,PMF和MDS/MPN亚型患者最有可能出现DAT阳性结果和自身免疫表现(≥50%)。PV和ET患者出现自身免疫表现的可能性较低(≤10%)。与血栓形成的发生没有相关性。
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