دورية أكاديمية
Erythroferrone and hepcidin as mediators between erythropoiesis and iron metabolism during allogeneic hematopoietic stem cell transplant.
| العنوان: | Erythroferrone and hepcidin as mediators between erythropoiesis and iron metabolism during allogeneic hematopoietic stem cell transplant. |
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| المؤلفون: | PIROTTE, Michelle, Fillet, Marianne, SEIDEL, Laurence, JASPERS, Aurélie, Baron, Frédéric, Beguin, Yves |
| المصدر: | American Journal of Hematology, 96 (10), 1275-1286 (2021) |
| بيانات النشر: | John Wiley & Sons, 2021. |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | Adult, Aged, Erythropoiesis/drug effects, Erythropoietin/therapeutic use, Female, Hematopoietic Stem Cell Transplantation, Hepcidins/blood/metabolism, Humans, Iron/blood/metabolism, Male, Middle Aged, Peptide Hormones/blood/metabolism, Transplantation, Homologous, Human health sciences, Hematology, Sciences de la santé humaine, Hématologie |
| الوصف: | Hematopoietic cell transplantation (HCT) brings important alterations in erythropoiesis and iron metabolism. Hepcidin, which regulates iron metabolism, increases in iron overload or inflammation and decreases with iron deficiency or activated erythropoiesis. Erythroferrone (ERFE) is the erythroid regulator of hepcidin. We investigated erythropoiesis and iron metabolism after allogeneic HCT in 70 patients randomized between erythropoietin (EPO) treatment or no EPO, by serially measuring hepcidin, ERFE, CRP (inflammation), soluble transferrin receptor (sTfR, erythropoiesis), serum iron and transferrin saturation (Tsat; iron for erythropoiesis) and ferritin (iron stores). We identified biological and clinical factors associated with serum hepcidin and ERFE levels. Serum ERFE correlated overall with sTfR and reticulocytes and inversely with hepcidin. Erythroferrone paralleled sTfR levels, dropping during conditioning and recovering with engraftment. Inversely, hepcidin peaked after conditioning and decreased during engraftment. Erythroferrone and hepcidin were not significantly different with or without EPO. Multivariate analyses showed that the major determinant of ERFE was erythropoiesis (sTfR, reticulocytes or serum Epo). Pretransplant hepcidin was associated with previous RBC transfusions and ferritin. After transplantation, the major determinants of hepcidin were iron status (ferritin at all time points and Tsat at day 56) and erythropoiesis (sTfR or reticulocytes or ERFE), while the impact of inflammation was less clear and clinical parameters had no detectable influence. Hepcidin remained significantly higher in patients with high compared to low pretransplant ferritin. After allogeneic HCT with or without EPO therapy, significant alterations of hepcidin occur between pretransplant and day 180, in correlation with iron status and inversely with erythroid ERFE. |
| نوع الوثيقة: | journal article http://purl.org/coar/resource_type/c_6501Test article peer reviewed |
| اللغة: | English |
| العلاقة: | urn:issn:0361-8609; urn:issn:1096-8652 |
| DOI: | 10.1002/ajh.26300 |
| الوصول الحر: | https://orbi.uliege.be/handle/2268/265879Test |
| حقوق: | open access http://purl.org/coar/access_right/c_abf2Test info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsorb.265879 |
| قاعدة البيانات: | ORBi |
| DOI: | 10.1002/ajh.26300 |
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