Polycythemia risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
There are no established risk factors for | There are no established risk factors for Polycythemia vera except for the genetic abnormality JAK2V617F. | ||
==Risk Factors== | ==Risk Factors== |
Revision as of 21:41, 10 December 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Debduti Mukhopadhyay, M.B.B.S[2]
Overview
There are no established risk factors for Polycythemia vera except for the genetic abnormality JAK2V617F.
Risk Factors
- One of the most common and most dangerous complications of polycythemia vera is thrombus formation. The risk factors are as follows:
- Women- usually younger at the time of diagnosis, have a higher risk of arterio-venous thrombosis.
- Mutation- higher burden of JAK2V617F allele
- Inflammatory markers- Pentraxins play an important role: increased hs-CRP and a lower PTX3 have a higher risk of thrombosis
- Presence of microparticles- responsible for decreased thrombin inhibition, increased CD41, and an increased chance of splenomegaly
- Neutrophil Extracellular Trap formations- NETosis and apoptosis [1]