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Published on: December 4, 2015
The role of red blood cell polymorphisms in resistance and susceptibility to malaria
B Lell1, J May, R J Schmidt-Ott
1Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Germany.
Insights
Red cell polymorphisms like sickle cell trait and blood group A influence malaria severity in children. Sickle cell trait is linked to milder malaria, while blood group A is associated with severe cases.
Area of Science:
- Malariology
- Human Genetics
- Epidemiology
Background:
- Regions endemic for Plasmodium falciparum malaria exhibit widespread red cell polymorphisms conferring resistance to severe disease.
- Understanding these genetic factors is crucial for managing malaria's public health impact.
Purpose of the Study:
- To investigate the association between specific red cell polymorphisms and the severity of Plasmodium falciparum malaria in Gabonese children.
- To evaluate the impact of these polymorphisms on reinfection rates and disease presentation.
Main Methods:
- Determined sickle cell trait, alpha-thalassemia, glucose-6-phosphate dehydrogenase deficiency, and blood groups in 100 children with severe malaria and 100 with mild malaria.
- Matched cases and controls, followed up for reinfections, parasitemia, and hematocrit levels.
Main Results:
- Sickle cell trait was significantly associated with mild malaria; blood group A was linked to severe malaria.
- Children with severe malaria experienced higher reinfection rates, higher parasitemia, and lower hematocrit levels upon follow-up.
- Sickle cell trait correlated with lower parasitemia levels, irrespective of reinfection incidence.
Conclusions:
- Malaria severity is partly determined by the presence of blood group A and sickle cell trait.
- Differential reinfection patterns suggest varying host susceptibility to malaria based on prior disease severity and red cell polymorphisms.
Abstract:
In regions highly endemic for Plasmodium falciparum malaria, red cell polymorphisms that confer resistance to severe disease are widespread. Sickle cell trait, alpha-thalassemia, glucose-6-phosphate dehydrogenase deficiency, and blood groups were determined in 100 children from Gabon with severe malaria who were matched with 100 children with mild malaria and followed up for evaluation of reinfections. The sickle cell trait was significantly associated with mild malaria and blood group A with severe malaria. During follow-up, the original severe cases had significantly higher rates of reinfection than the original mild cases, with higher parasitemia and lower hematocrit values. Incidence rates did not differ in the context of erythrocyte polymorphisms, but patients with sickle cell trait presented with markedly lower levels of parasitemia than those without. Thus, the severity of malaria is partly determined by the presence of blood group A and the sickle cell trait. The different presentation of reinfections in severe versus mild cases probably reflects different susceptibility to malaria.
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