1999
DOI: 10.1002/(sici)1520-6661(199901/02)8:1<1::aid-mfm1>3.0.co;2-o
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Induction of fetal hemoglobin synthesis with recombinant human erythropoietin in anemic patients with heterozygous beta-thalassemia during pregnancy

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Cited by 17 publications
(6 citation statements)
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“…However, in these patients Epo stimulates thalassemic erythropoiesis with production of abnormal RBC having excess α -globin chains, membrane damage, and short survival. As for stimulation of fetal Hb, contradictory results were reported [ 8 , 42 , 43 ]. Our findings raise the possibility that Epo administration may benefit thalassemic patients also by reducing oxidative stress and thereby prolonging the survival of their RBC as well as lowering the state of activation of their platelets.…”
Section: Discussionmentioning
confidence: 99%
“…However, in these patients Epo stimulates thalassemic erythropoiesis with production of abnormal RBC having excess α -globin chains, membrane damage, and short survival. As for stimulation of fetal Hb, contradictory results were reported [ 8 , 42 , 43 ]. Our findings raise the possibility that Epo administration may benefit thalassemic patients also by reducing oxidative stress and thereby prolonging the survival of their RBC as well as lowering the state of activation of their platelets.…”
Section: Discussionmentioning
confidence: 99%
“…Inappropriately low serum erythropoietin levels may be found in SCD (de Klerk et al 1981) and erythropoietin increases fetal haemoglobin levels (Breymann et al 1999). The increase in both fetal and total haemoglobin makes erythropoietin therapy a useful treatment in SCD.…”
Section: Discussionmentioning
confidence: 99%
“…Current Protocols in Cytometry of therapies, such as hydroxyurea, having the specific therapeutic intent of raising F-cell levels (Atweh et al, 1999;Iyamu et al, 2000;. The increase in F-cell or HbF levels parallels an improved clinical course in both sickle cell disease and thalassemia (Breymann et al, 1999;Nagel et al, 1993); however, since the therapies that induce increased F cells and HbF all have toxic side effects, it follows that therapeutic monitoring by F-cell enumeration should facilitate more optimal dosing for these patients. Additionally, F-cell assays could identify patients not requiring such therapies by virtue of preexisting constitutive production of F cells due to their genetic constitution.…”
Section: Of 17mentioning
confidence: 99%