Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesis

被引:47
作者
Cazzola, M [1 ]
Beguin, Y
Bergamaschi, G
Guarnone, R
Cerani, P
Barella, S
Cao, A
Galanello, R
机构
[1] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[2] Univ Pavia, Sch Med, Dept Internal Med & Med Therapy, Anaemia Unit, I-27100 Pavia, Italy
[3] Univ Liege, Dept Med, Div Haematol, Liege, Belgium
[4] Univ Cagliari, Ist Clin & Biol Eta Evolut, I-09100 Cagliari, Italy
关键词
anaemia; erythropoiesis; erythropoietin; iron overload; soluble transferrin receptor;
D O I
10.1046/j.1365-2141.1999.01600.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital anaemias due to ineffective erythropoiesis may be associated with excessive iron absorption and progressive iron loading. We investigated whether the soluble transferrin receptor (TfR) level was related to the degree of iron overload in 20 patients with thalassaemia intermedia, six patients with congenital dyserythropoietic anaemia type II (CDA II) and four patients with X-linked congenital sideroblastic anaemia (XLSA). All but two patients had increased serum ferritin levels (median 601 mu g/l, range 105-2855 mu g/l). Multiple regression analysis showed that 62% (P<0.0001) of the variation in serum ferritin was explained by age and by changes in soluble TfR.
引用
收藏
页码:752 / 755
页数:4
相关论文
共 12 条
  • [1] BAYNES RD, 1995, P SOC EXP BIOL MED, V209, P286
  • [2] IRON LOADING IN CONGENITAL DYSERYTHROPOIETIC ANEMIAS AND CONGENITAL SIDEROBLASTIC ANEMIAS
    CAZZOLA, M
    BAROSI, G
    BERGAMASCHI, G
    DEZZA, L
    PALESTRA, P
    POLINO, G
    RAMELLA, S
    SPRIANO, P
    ASCARI, E
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1983, 54 (04) : 649 - 654
  • [3] The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
    Feder, JN
    Penny, DM
    Irrinki, A
    Lee, VK
    Lebrón, JA
    Watson, N
    Tsuchihashi, Z
    Sigal, E
    Bjorkman, PJ
    Schatzman, RC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) : 1472 - 1477
  • [4] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    Feder, JN
    Gnirke, A
    Thomas, W
    Tsuchihashi, Z
    Ruddy, DA
    Basava, A
    Dormishian, F
    Domingo, R
    Ellis, MC
    Fullan, A
    Hinton, LM
    Jones, NL
    Kimmel, BE
    Kronmal, GS
    Lauer, P
    Lee, VK
    Loeb, DB
    Mapa, FA
    McClelland, E
    Meyer, NC
    Mintier, GA
    Moeller, N
    Moore, T
    Morikang, E
    Prass, CE
    Quintana, L
    Starnes, SM
    Schatzman, RC
    Brunke, KJ
    Drayna, DT
    Risch, NJ
    Bacon, BR
    Wolff, RK
    [J]. NATURE GENETICS, 1996, 13 (04) : 399 - 408
  • [5] FINCH C, 1994, BLOOD, V84, P1697
  • [6] HUEBERS HA, 1990, BLOOD, V75, P102
  • [7] Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor
    Lebrón, JA
    Bennett, MJ
    Vaughn, DE
    Chirino, AJ
    Snow, PM
    Mintier, GA
    Feder, JN
    Bjorkman, PJ
    [J]. CELL, 1998, 93 (01) : 111 - 123
  • [8] PETO TEA, 1983, LANCET, V1, P375
  • [9] PIPPARD MJ, 1979, LANCET, V2, P819
  • [10] POOTRAKUL P, 1988, BLOOD, V71, P1124