Title |
Hydroxyurea treatment in β-thalassemia patients: to respond or not to respond?
|
---|---|
Published in |
Annals of Hematology, January 2013
|
DOI | 10.1007/s00277-012-1671-3 |
Pubmed ID | |
Authors |
Mehdi Banan |
Abstract |
Hydroxyurea (HU) is a drug that induces fetal hemoglobin production. As a result, HU is widely used to treat β-thalassemia (β-thal) patients. However, the response of these patients to HU varies. Some β-thal patients respond favorably to treatment while others do not respond at all. HU has a number of side-effects and therefore its targeted prescription is beneficial. Hence, identifying the genetic determinants which lead to the differential HU response is important. This review summarizes recent findings which have shed light on this topic. Special emphasis is given to the mechanisms and genetic loci which may govern these differences. These findings have helped identify several single nucleotide polymorphisms which associate with the response to HU in both β-thal and sickle cell disease patients. |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 48 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Master | 6 | 13% |
Other | 5 | 10% |
Student > Doctoral Student | 5 | 10% |
Student > Ph. D. Student | 5 | 10% |
Student > Bachelor | 4 | 8% |
Other | 8 | 17% |
Unknown | 15 | 31% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 11 | 23% |
Biochemistry, Genetics and Molecular Biology | 10 | 21% |
Agricultural and Biological Sciences | 4 | 8% |
Nursing and Health Professions | 2 | 4% |
Pharmacology, Toxicology and Pharmaceutical Science | 2 | 4% |
Other | 3 | 6% |
Unknown | 16 | 33% |