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Association between JAK2V617F mutation and thrombotic complication in patients with classical Ph-negative chronic myeloproliferative diseases

https://doi.org/10.25789/YMJ.2020.69.04

Abstract

The study was conducted with aim to assess the effect of clinical and laboratory parameters and JAK2V617F mutation on the incidence of thrombotic complications in patients with classical Ph-negative chronic myeloproliferative diseases. JAK2V617F mutation was detected in patients with polycythemia vera, essential thrombocythemia and patients with primary myelofibrosis. Thrombotic complications were significantly more often observed in carriers of the JAK2V617F mutation and in patients with cardiovascular risk factors.

About the Authors

T. N. Aleksandrova
Yakut Science Centre of complex medical problems; National Centre of Medicine
Russian Federation

ALEKSANDROVA Tuiara Nikonovna – junior researcher of the laboratory of heritable pathology Yakut Science Centre of complex medical problems, hematologist of National Centre of Medicine



I. I. Mulina
National centre of Medicine
Russian Federation

MULINA Inna Ivanovna – Head of the Department of hematology 



K. A. Kurtanov
Yakut Science Centre of complex medical problems
Russian Federation

KURTANOV Khariton Alekseevich – Candidate of medical sciences, chief researcher – Head of department of molecular genetics



I. E. Solovieva
National centre of Medicine
Russian Federation

SOLOVIEVA Irina Eremeevna – hematologist



L. D. Terekhova
National centre of Medicine
Russian Federation


N. I. Pavlova
Yakut Science Centre of complex medical problems
Russian Federation

PAVLOVA Nadezhda Ivanovna – Candidate of Biological Sciences, leading researcher, Head of hereditary pathology laboratory



V. N. Yadrikinskaya
North-Eastern Federal University
Russian Federation

YADRIKHINSKAYA Vera Nikolaevna – candidate of medical sciences, associate professor of department «Hospital therapy, professional diseases, clinical pharmacology» Medical Institute



N. A. Solovieva
Yakut Science Centre of complex medical problems
Russian Federation

SOLOVIEVA Natalya Alekseevna – researcher of the Laboratory of Population Genetics



A. T. Dyakonova
Yakut Science Centre of complex medical problems
Russian Federation

DYAKONOVA Aleksandra Timofeevna – junior researcher of the laboratory of heritable pathology



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Review

For citations:


Aleksandrova T.N., Mulina I.I., Kurtanov K.A., Solovieva I.E., Terekhova L.D., Pavlova N.I., Yadrikinskaya V.N., Solovieva N.A., Dyakonova A.T. Association between JAK2V617F mutation and thrombotic complication in patients with classical Ph-negative chronic myeloproliferative diseases. Yakut Medical Journal. 2020;(1):21-23. https://doi.org/10.25789/YMJ.2020.69.04

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ISSN 1813-1905 (Print)
ISSN 2312-1017 (Online)