Hepcidin and Erythropoietin Level in Sickle Cell Disease.
Br J Med Med Res
;
2015; 8(3): 261-265
Artículo
en Inglés
| IMSEAR
| ID: sea-180601
ABSTRACT
Background:
Sickle cell anaemia is an inherited disorder in which the red blood cells become rigid and sticky, and change from being disc-shaped to being crescent-shaped. The change in shape is as a result of an abnormal form of haemoglobin which leads to damage of some organs.Aim:
The study was carried out to determine the levels of hepcidin and erythropoietin in sickle cell anemia. Materials andMethods:
Thirty confirmed sickle cell patients in steady state (HbSS-SS) and thirty persons with normal hemoglobin (HbAA) between the ages of 15 to 30 years were selected in this study.Results:
The results obtained showed that the levels of hepcidinin sickle cell anaemia patients were significantly elevated when compared with normal haemoglobin (HbAA) (P<0.05). However, the levels of erythropoietin were significantly decreased in sickle cell anaemia stable state when compared to HbAA subjects (P<0.05).Conclusion:
This could probably imply that the elevation in hepcidin affect level of erythropoietin negatively. Therefore, it is possible that an antihepcidin could be developed as a therapeutic tool in sickle cell anaemia.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Idioma:
Inglés
Revista:
Br J Med Med Res
Año:
2015
Tipo del documento:
Artículo
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