A refined diagnostic algorithm for polycythemia vera that incorporates mutation screening for JAK2(V617F)

Curr Hematol Malig Rep. 2006 Jun;1(2):81-6. doi: 10.1007/s11899-006-0027-2.

Abstract

Historically, red cell mass (RCM) measurement has been promoted as an accurate indicator of the body's red cell content. Both the Polycythemia Vera Study Group and a committee sponsored by the World Health Organization have endorsed its inclusion in their diagnostic criteria without supporting evidence of diagnostic accuracy from a systematic study. Over the years, it has become evident that RCM measurement is a cumbersome and costly test and, as a result, it has been abandoned by many hematologists in practice. The recent discovery that a somatic JAK2-activating mutation, JAK2(V617F), is almost invariably associated with polycythemia vera further supports the use of diagnostic algorithms that are based on biologic parameters in place of traditional diagnostic criteria that are based on RCM measurement. Therefore, a contemporary approach to the diagnosis of polycythemia vera starts with peripheral blood mutation screening for JAK2(V617F) as well as measurement of serum erythropoietin. The results of these tests, along with the clinical scenario, determine the need for further investigation, including bone marrow examination.

Publication types

  • Review

MeSH terms

  • Algorithms*
  • Amino Acid Substitution
  • Bone Marrow Examination
  • Diagnosis, Differential
  • Erythrocyte Volume
  • Erythropoietin / blood*
  • Hematocrit
  • Humans
  • Janus Kinase 2 / chemistry
  • Janus Kinase 2 / genetics*
  • Janus Kinase 2 / physiology
  • Mutation, Missense*
  • Point Mutation*
  • Polycythemia Vera / blood
  • Polycythemia Vera / diagnosis*
  • Polycythemia Vera / enzymology
  • Polycythemia Vera / genetics
  • Predictive Value of Tests
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Erythropoietin
  • JAK2 protein, human
  • Janus Kinase 2