Literature DB >> 36136222

Characteristics of patients with cerebral sinus venous thrombosis and JAK2 V617F mutation.

Naaem Simaan1,2, Jeremy Molad3, Asaf Honig4, Andrei Filioglo4, Fadi Shbat1,2, Eitan Auriel5,6, Rani Barnea5,6, Hen Hallevi3,6, Estelle Seyman4, Rom Mendel5,6, Ronen R Leker7, Shlomi Peretz5,6.   

Abstract

OBJECTIVES: 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.
MATERIALS AND METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.
© 2022. The Author(s) under exclusive licence to Belgian Neurological Society.

Entities:  

Keywords:  Cerebral sinus venous thrombosis; Intracerebral hemorrhage; Mutation; Stroke

Year:  2022        PMID: 36136222     DOI: 10.1007/s13760-022-02077-x

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN: 0300-9009            Impact factor:   2.471


  16 in total

Review 1.  The role of JAK2 V617F mutation, spontaneous erythropoiesis and megakaryocytopoiesis, hypersensitive platelets, activated leukocytes, and endothelial cells in the etiology of thrombotic manifestations in polycythemia vera and essential thrombocythemia.

Authors:  Sylvia Bellucci; Jan J Michiels
Journal:  Semin Thromb Hemost       Date:  2006-06       Impact factor: 4.180

Review 2.  Implications of Janus Kinase 2 Mutation in Embolic Stroke of Unknown Source.

Authors:  Gabriela Trifan; Neelofer Shafi; Fernando D Testai
Journal:  J Stroke Cerebrovasc Dis       Date:  2018-07-26       Impact factor: 2.136

3.  Features of intracranial hemorrhage in cerebral venous thrombosis.

Authors:  K Afifi; G Bellanger; P J Buyck; S M Zuurbier; C G Esperon; M A Barboza; P Costa; I Escudero; D Renard; R Lemmens; N Hinteregger; F Fazekas; J Jimenez Conde; E Giralt-Steinhauer; S Hiltunen; A Arauz; A Pezzini; J Montaner; J Putaala; C Weimar; Marc Schlamann; T Gattringer; T Tatlisumak; J M Coutinho; P Demaerel; V Thijs
Journal:  J Neurol       Date:  2020-06-22       Impact factor: 4.849

4.  The JAK2 V617F mutation in patients with cerebral venous thrombosis.

Authors:  S M Passamonti; E Biguzzi; M Cazzola; F Franchi; F Gianniello; P Bucciarelli; D Pietra; P M Mannucci; I Martinelli
Journal:  J Thromb Haemost       Date:  2012-06       Impact factor: 5.824

5.  Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders.

Authors:  V De Stefano; A Fiorini; E Rossi; T Za; G Farina; P Chiusolo; S Sica; G Leone
Journal:  J Thromb Haemost       Date:  2007-01-29       Impact factor: 5.824

6.  Should We Screen for Janus Kinase 2 V617F Mutation in Cerebral Venous Thrombosis?

Authors:  Matthias Lamy; Paola Palazzo; Pierre Agius; Jean Claude Chomel; Jonathan Ciron; Aline Berthomet; Paul Cantagrel; Julia Prigent; Pierre Ingrand; Mathieu Puyade; Jean-Philippe Neau
Journal:  Cerebrovasc Dis       Date:  2017-06-14       Impact factor: 2.762

7.  JAK2 mutations across a spectrum of venous thrombosis cases.

Authors:  Shrimati Shetty; Bipin Kulkarni; Navin Pai; Preeti Mukundan; Priyanka Kasatkar; Kanjaksha Ghosh
Journal:  Am J Clin Pathol       Date:  2010-07       Impact factor: 2.493

Review 8.  Clinical and laboratory features, pathobiology of platelet-mediated thrombosis and bleeding complications, and the molecular etiology of essential thrombocythemia and polycythemia vera: therapeutic implications.

Authors:  Jan J Michiels; Zwi Berneman; Dirk Van Bockstaele; Marc van der Planken; Hendrik De Raeve; Wilfried Schroyens
Journal:  Semin Thromb Hemost       Date:  2006-04       Impact factor: 4.180

Review 9.  Leukocytosis, JAK2V617F mutation, and hemostasis in myeloproliferative disorders.

Authors:  Marina Marchetti; Anna Falanga
Journal:  Pathophysiol Haemost Thromb       Date:  2009-01-27

10.  Low prevalence of JAK2 V617F mutation in patients with thrombosis and normal blood counts: a retrospective impact study.

Authors:  Michaël Levraut; Laurence Legros; Charles Drappier; Marie C Béné; Viviane Queyrel; Sophie Raynaud; Nihal Martis
Journal:  J Thromb Thrombolysis       Date:  2020-04-07       Impact factor: 2.300

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