Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen-sensing pathway from primary familial and congenital polycythaemia
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
37246471
DOI
10.1111/bjh.18891
Knihovny.cz E-resources
- Keywords
- EPOR, VHL, erythrocytosis, erythroferrone, hepcidin,
- MeSH
- Hepcidins genetics MeSH
- Ion Channels genetics MeSH
- Oxygen metabolism MeSH
- Humans MeSH
- Mutation MeSH
- Polycythemia * genetics congenital MeSH
- Receptors, Erythropoietin genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Hepcidins MeSH
- Ion Channels MeSH
- Oxygen MeSH
- PIEZO1 protein, human MeSH Browser
- Receptors, Erythropoietin MeSH
Congenital erythrocytoses represent a heterogenous group of rare defects of erythropoiesis characterized by elevated erythrocyte mass. We performed molecular-genetic analysis of 21 Czech patients with congenital erythrocytosis and assessed the mutual link between chronic erythrocyte overproduction and iron homoeostasis. Causative mutations in erythropoietin receptor (EPOR), hypoxia-inducible factor 2 alpha (HIF2A) or Von Hippel-Lindau (VHL) genes were detected in nine patients, including a novel p.A421Cfs*4 EPOR and a homozygous intronic c.340+770T>C VHL mutation. The association and possible cooperation of five identified missense germline EPOR or Janus kinase 2 (JAK2) variants with other genetic/non-genetic factors in erythrocytosis manifestation may involve variants of Piezo-type mechanosensitive ion channel component 1 (PIEZO1) or Ten-eleven translocation 2 (TET2), but this requires further research. In two families, hepcidin levels appeared to prevent or promote phenotypic expression of the disease. No major contribution of heterozygous haemochromatosis gene (HFE) mutations to the erythrocytic phenotype or hepcidin levels was observed in our cohort. VHL- and HIF2A-mutant erythrocytosis showed increased erythroferrone and suppressed hepcidin, whereas no overproduction of erythroferrone was detected in other patients regardless of molecular defect, age or therapy. Understanding the interplay between iron metabolism and erythropoiesis in different subgroups of congenital erythrocytosis may improve current treatment options.
Department of Biology Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic
Department of Haemato Oncology University Hospital Olomouc Olomouc Czech Republic
Department of Immunology Faculty of Medicine and Dentistry Palacky University Olomouc Czech Republic
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