Simaan Naaem, Molad Jeremy, Honig Asaf, Filioglo Andrei, Shbat Fadi, Auriel Eitan, Barnea Rani, Hallevi Hen, Seyman Estelle, Mendel Rom, Leker Ronen R, Peretz Shlomi
Department of Neurology, Ziv Medical Center, Safed, Israel.
The Azrieli Faculty of Medicine, Bar Ilan University, Safed, Israel.
Acta Neurol Belg. 2023 Oct;123(5):1855-1859. doi: 10.1007/s13760-022-02077-x. Epub 2022 Sep 22.
Janus kinase 2 (JAK2-V617F) mutations can cause thrombocytosis, polycythemia and hyper viscosity leading to cerebral sinus venous thrombosis (CSVT). However, data regarding the characteristics and prevalence of JAK2-V617F mutation in patients with CSVT are currently lacking. We aimed to evaluate the characteristics of CSVT patients that carry the JAK2 mutation.
Data of consecutive patients with CSVT, admitted to three large academic medical centers between 2010 and 2020, were retrospectively studied. Demographics, clinical presentations, radiological and clinical outcome parameters were compared between carriers of the JAK2-V617F mutation and controls.
Out of 404 patients diagnosed with CSVT, 26 patients (6.5%) were carriers of the mutation. JAK2 mutation carriers more often had thrombocytosis (54% vs. 1%, p < 0.001). Furthermore, carriers of the JAK2 mutation less often had involvement of the transverse sinus (50% vs. 68%, p = 0.021). Finally, patients with the JAK2 mutation were more prone to have intracerebral hemorrhage (ICH, 31% vs. 17%, p = 0.044), but there was no significant difference between groups in terms of mortality nor functional outcome.
JAK2 mutation is not uncommon in patients with CSVT and should be routinely screened for in this population. CSVT in JAK2 mutation carriers may have a tendency toward involving specific venous sinuses and is associated with a higher rate of ICH but similar overall prognosis.
Janus激酶2(JAK2-V617F)突变可导致血小板增多、红细胞增多症和高黏滞血症,进而引发脑静脉窦血栓形成(CSVT)。然而,目前缺乏关于CSVT患者中JAK2-V617F突变特征和患病率的数据。我们旨在评估携带JAK2突变的CSVT患者的特征。
回顾性研究了2010年至2020年间入住三家大型学术医学中心的连续性CSVT患者的数据。比较了JAK2-V617F突变携带者与对照组之间的人口统计学、临床表现、影像学和临床结局参数。
在404例诊断为CSVT的患者中,26例(6.5%)为该突变携带者。JAK2突变携带者更常出现血小板增多症(54%对1%,p<0.001)。此外,JAK2突变携带者较少出现横窦受累(50%对68%,p=0.021)。最后,JAK2突变患者更容易发生脑出血(ICH,31%对17%,p=0.044),但两组在死亡率和功能结局方面无显著差异。
JAK2突变在CSVT患者中并不少见,应在该人群中进行常规筛查。JAK2突变携带者的CSVT可能倾向于累及特定静脉窦,并与较高的ICH发生率相关,但总体预后相似。