Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I
- 15 December 2008
- journal article
- Published by American Society of Hematology in Blood
- Vol. 112 (13) , 5241-5244
- https://doi.org/10.1182/blood-2008-06-165738
Abstract
Congenital dyserythropoietic anemia (CDA) is a rare group of red blood cell disorders characterized by ineffective erythropoiesis and increased iron absorption. To determine whether growth differentation factor 15 (GDF15) hyper-expression is associated with the ineffective erythropoiesis and iron-loading complications of CDA type I (CDA I), GDF15 levels and other markers of erythropoiesis and iron overload were studied in blood from 17 CDA I patients. Significantly higher levels of GDF15 were detected among the CDA I patients (10 239 ± 3049 pg/mL) compared with healthy volunteers (269 ± 238 pg/mL). In addition, GDF15 correlated significantly with several erythropoietic and iron parameters including Hepcidin-25, Ferritin, and Hepcidin-25/Ferritin ratios. These novel results suggest that CDA I patients express very high levels of serum GDF15, and that GDF15 contributes to the inappropriate suppression of hepcidin with subsequent secondary hemochromatosis.Keywords
This publication has 17 references indexed in Scilit:
- Advances in Quantitative Hepcidin Measurements by Time-of-Flight Mass SpectrometryPLOS ONE, 2008
- Erythropoietin mediates hepcidin expression in hepatocytes through EPOR signaling and regulation of C/EBPαBlood, 2008
- Regulation of hepcidin: Insights from biochemical analyses on human serum samplesBlood Cells, Molecules, and Diseases, 2008
- Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)European Journal of Haematology, 2007
- Liver iron concentrations and urinary hepcidin in -thalassemiaHaematologica, 2007
- Hypocholesterolemia in chronic anemias with increased erythropoietic activityAmerican Journal of Hematology, 2006
- Clinical and molecular variability in congenital dyserythropoietic anaemia type IBritish Journal of Haematology, 2005
- Hepcidin in iron overload disordersBlood, 2005
- Hepcidin is decreased in TFR2 hemochromatosisBlood, 2005
- Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1American Journal of Human Genetics, 2002