Pulsed-dosing with oral sodium phenylbutyrate increases hemoglobin F in a patient with sickle cell anemia |
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Authors: | Hines Patrick Dover George J Resar Linda M S |
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Affiliation: | Hematology Division, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. |
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Abstract: | Increasing hemoglobin F (HbF) appears to be beneficial for patients with sickle cell anemia. We previously demonstrated that daily, oral sodium phenylbutyrate (OSPB) induces HbF synthesis in pediatric and adult patients with hemoglobin SS (HbSS). The high doses and need for daily therapy, however, have limited its use. Here, we report a patient treated with pulsed-dosing of OSPB for over 3 years. This patient developed a modest, but sustained elevation in HbF over the course of therapy without side effects. Although larger studies are needed, this case demonstrates that pulsed-dosing with OSPB enhances HbF synthesis. |
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Keywords: | hemoglobin F pulsed‐dosing sickle cell anemia sodium phenylbutyrate |
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