Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)

Congenital erythrocytosis can be classified as primary, when the defect is intrinsic to the RBC progenitors and independent of the serum erythropoietin ( E po) concentration, or secondary, when the erythrocytosis is the result of an upregulation of E po production. Primary erythrocytosis is associated with mutations in the EPOR gene, secondary CE can de due to mutations that stabilize the hemoglobin in the oxygenated form or to mutations in the genes that control the transcriptional activation of the EPO gene – VHL , EGLN1 , EPAS1 . Chuvash polycythemia, caused by mutations in VHL gene, shares features of both primary and secondary erythrocytosis, with increased E po production but also hypersensitivity of progenitors to E po. Material and Methods With the main objective of describing the etiology and molecular basis of CE , we have studied 70 consecutive unrelated patients presenting with idiopathic erythrocytosis from our hematology clinic or referred from other centers. According to a study algorithm, we have sequenced all the genes described as associated with CE . Results and Discussion Erythrocytosis molecular etiology was identify in 25 (36%) of the 70 subjects. High‐affinity H b variants were the most common cause, present in 20% of the cases. New mutations were identified in the JAK2 , EPOR , VHL , and EGLN1 genes. Conclusions High‐affinity hemoglobin variants are a very rare cause of secondary CE , but it seems likely that their incidence may be underestimated. Our experience shows that in erythrocytosis with a dominant inheritance and normal or inappropriate high Epo levels, the HBB and HBA genes should be the first to be studied. In spite of the seven genes known to be involved in CE , the majority of the cases have unknown etiology.