Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors

Abstract

The single base molecular substitution characterizing sickle cell haemoglobin, β⁶glu→val, might be expected to result in predictable haematological and clinical features. However, the disease manifests remarkable diversity believed to reflect the interaction with other genetic and environmental factors. Some of the genetic modifiers include the beta globin haplotypes, alpha thalassaemia, factors influencing the persistence of fetal haemoglobin and the effects of the environment are addressed in this review. It is concluded that much of the genetic data present conflicting results. Environmental factors such as climate and infections, and psychological, educational and social support mechanisms also influence expression of the disease. These interactions illustrate how the expression of a 'single gene' disorder may be influenced by a variety of other genetic and environmental factors.

Keywords: Alpha thalassaemia; Beta globin haplotypes; Environmental factors; Fetal haemoglobin; Sickle cell disease.