G. Nisli et al., SERUM ERYTHROPOIETIN LEVELS IN PATIENTS WITH BETA-THALASSEMIA MAJOR AND INTERMEDIA, Pediatric hematology and oncology, 14(2), 1997, pp. 161-167
Serum etythropoietin (EPO) levels were determined by radioimmunoassay
in 37 beta-thalassemia patients, the phenotype being thalassemia major
(TM) in 30 and thalassemia intermedia (TI) in 7. The control group co
nsisted of 37 healthy children. The mean serum EPO levels were signifi
cantly higher in patients with both TM (215.1+/-144.5) and TI (53.8+/-
40.2) compared with the control group (9.3 +/- 4.6). Although the mean
hemoglobin (Hb) concentrations in the patients with TM and TI were si
milar (8.6+/-0.9 and 8.7+/-1.1, respectively), the mean serum EPO leve
l was significantly higher in TM patients than the patients with TI (P
<.01). This finding may indicate that some other factors contributing
to the metabolic adaptation to low oxygen concentration or improvement
of the tissue oxygenation are as effective as the Hb concentration in
EPO production. It is also suggestive of the fact that some amount of
tissue hypoxia cannot be prevented in spite of polytransfusion regime
ns in TM patients. Serum EPO levels of TM patients were not found to b
e age related or correlated with the mean pretransfusional Hb levels.
In the TM patients, the serum EPO concentration was not consistently c
orrelated with clinical signs of erythropoietic activity. This may be
indicative of personal differences with respect to the sensitivities o
f erythroid precursors to the increasing EPO levels in TM patients.