Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I

被引:105
作者
Tamary, Hannah [1 ]
Shalev, Hanna [2 ]
Perez-Avraham, Galit [2 ]
Zoldan, Meira [1 ]
Levi, Itai [2 ]
Swinkels, Dorine W. [3 ]
Tanno, Toshihiko [4 ]
Miller, Jeffery L. [4 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Schneider Childrens Med Ctr Israel Petah Tikva, Hematol Oncol Ctr, IL-69978 Tel Aviv, Israel
[2] Ben Gurion Univ Negev, Hematol Soroka Med Ctr, Fac Med, IL-84105 Beer Sheva, Israel
[3] Radboud Univ Nijmegen, Dept Clin Chem, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[4] NIDDK, Mol Med Branch, NIH, Bethesda, MD USA
关键词
D O I
10.1182/blood-2008-06-165738
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (Blood. 2008; 112: 5241-5244)
引用
收藏
页码:5241 / 5244
页数:4
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