α Thalassemia and the hematology of homozygous sickle cell disease in childhood
Stevens MCG., Maude GH., Beckford M., Grandison Y., Mason K., Taylor B., Serjeant BE., Higgs DR., Teal H., Weatherall DJ.
α Thalassemia modifies the hematologic expression of homozygous sickle cell (SS) disease, resulting in increased total hemoglobin and HbA2 and decreased HbF, mean cell volume, reticulocytes, irreversibly sickled cells, and bilirubin levels. The age at which these changes develop in children with SS disease is unknown. Ascertainment of globin gene status in a large representative sample of children with SS disease has afforded an opportunity to study the hematologic indices in nine children homozygous for α thalassemia 2 (two-gene group), 90 children heterozygous for α thalassemia 2 (three-gene group), and 167 children with a normal α globin gene complement (four-gene group). The two-gene group had significantly lower mean cell volumes from birth, higher red cell counts from one month, lower reticulocytes from three months, and higher HbA2 levels from one year, as compared with the four-gene group. Children with three genes had intermediate indices but resembled more closely the four-gene group. Differences in total hemoglobin or in fetal hemoglobin between the groups were not apparent by eight years of age. The most characteristic differences of the two-gene group were the raised proportional HbA2 level and low mean cell volume, the latter having some predictive value for α thalassemia status at birth.