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| Title: | Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I. |
| Author(s): | Tamary, H. Shalev, H. Perez-Avraham, G. Zoldan, M. Levi, I. Swinkels, D.W. (074142771) Tanno, T. Miller, J.L. |
| Publication year: | 2008 |
| Document type: | Article / Letter to editor |
| Journal: | Blood |
| ISSN: | 0006-4971 |
| Volume: | vol. 112 |
| Issue: | iss. 13 |
| Start page: | p. 5241 |
| End page: | p. 5244 |
| 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. |
| Subject: | UMCN 5.1: Genetic defects of metabolism |
| Organization: | UMCN Extern Clinical Chemistry |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/70405
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