Increased Fetal Hemoglobin in Patients Receiving Sodium 4-Phenylbutyrate
- 20 August 1992
- journal article
- letter
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 327 (8) , 569-570
- https://doi.org/10.1056/nejm199208203270818
Abstract
Increases in the production of fetal hemoglobin can ameliorate the severity of both sickle cell disease and β-thalassemia. Three groups of agents are known to increase the production of fetal hemoglobin in humans: cytotoxic drugs,1 , 2 growth factors,3 and agents that induce differentiation, such as butyrate.4 The clinical application of these drugs has been hindered by dose-limiting myelotoxicity or the requirement for continuous intravenous infusion. These difficulties may now be overcome through the exploitation of the recent discovery of sodium phenylacetate as a nontoxic inducer of differentiation affecting fetal hemoglobin production.5Keywords
This publication has 4 references indexed in Scilit:
- Prospective treatment of urea cycle disordersThe Journal of Pediatrics, 1991
- Diamond-Blackfan anemia: heterogenous response of hematopoietic progenitor cells in vitro to the protein product of the steel locusBlood, 1991
- Stimulation of F-Cell Production in Patients with Sickle-Cell Anemia Treated with Cytarabine or HydroxyureaNew England Journal of Medicine, 1985
- Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.Proceedings of the National Academy of Sciences, 1983