Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell Anaemia. (5th July 2012)

• Record Type: Journal Article
• Authors: Tshilolo, L.; Summa, V.; Gregorj, C.; Kinsiama, C.; Bazeboso, J. A.; Avvisati, G.; Labie, D.
• Other Names: Pace Betty S. Academic Editor.
• Is Part Of: Anemia. Volume 2012(2012)
• Publication Date: 2012-07-05
• Subjects: Anemia -- Periodicals; 616.152005
• DOI: 10.1155/2012/105349
• Languages: English
• ISSNs: 2090-1267

Abstract

Abstract : High HbF levels and F cells are correlated with reduced morbidity and mortality in sickle cell disease (SCD). This paper was designed to determine the HbF and F cells levels in Congolese sickle cell anemia (SCA) patients in order to determine their impact on the expression of SCD. Population and Method . HbF levels were measured in 89 SCA patients (mean age 11.4 yrs) using a standard HPLC method. F cell quantitation was done in a second group of SCA patients (n = 42, mean age 8.9 yrs) and compared with a control group (n = 47, mean age 5 yrs). F cells were quantified by a cytofluorometric system (MoAb-HbF—FITC; cut off at 0.5%). Results . The mean value of HbF was 7.2% ± 5.0 with heterogeneous distribution, most patients (76%) having HbF < 8%. Mean values of F-cells in SCA patients and control group were 5.4% ± 7.6 (median: 2.19% ; range 0, 0–30, 3%) and 0.5% ± 1.6 (median 0.0, range 0–5.18), respectively. SCA patients with F cells >4.5% developed less painful crisis and had higher percentage of reticulocytes. Conclusion . Congolese SCA patients displayed low levels of HbF and F-cells that contribute to the severity of SCD.