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Published on: December 4, 2015
[Morbidity and severity of malaria attacks in carriers of sickle-cell trait]
J P Chippaux1, A Massougbodji, J C Boulard
1ORSTOM, Antenne OCCGE de Cotonou, Bénin.
Insights
Children with sickle cell trait experience fewer malaria attacks and lower mortality rates compared to those with HbAA haemoglobin. This suggests sickle cell trait offers protection against Plasmodium falciparum malaria.
Area of Science:
- Medical Research
- Genetics
- Infectious Diseases
Context:
- High Plasmodium falciparum transmission area
- Pediatric outpatients (infirmary and hospital)
- Comparison of malaria frequency and severity across hemoglobin types
Purpose:
- To compare malaria attack frequency and severity in children with different hemoglobin types (HbAA vs. sickle cell trait).
- To investigate the role of hemoglobin type in malaria susceptibility and mortality.
- To determine the pathogenic parasitemia threshold in various hemoglobin types.
Summary:
- Malaria diagnosis was based on clinical, parasitological, and evolutionary criteria.
- A parasitemia threshold of approximately 3,000 infected red cells/mm³ was observed across all hemoglobin types.
- Malaria was diagnosed more frequently in HbAA children, who also had a higher mortality rate (>3%).
- Sickle cell trait carriers showed significantly lower S gene rates (5%) among malaria patients and no malaria-attributable deaths.
Impact:
- Sickle cell trait carriers exhibit reduced susceptibility to Plasmodium falciparum malaria.
- The S gene may confer a protective advantage against severe malaria outcomes.
- Findings contribute to understanding malaria epidemiology and host-parasite interactions in endemic regions.
Abstract:
The authors made a survey in a permanent high Plasmodium falciparum transmission area to compare frequency and severity of malaria attacks in children belonging to different haemoglobin types before 15 years; 291 young out-patients of the local infirmary and 467 outpatients of the hospital were examined. Diagnosis of malaria was inferred from clinical and parasitological criteria and subsequent evolution of the disease. Pathogenic threshold of parasitaemia was similar in all haemoglobin type groups of children and was about 3,000 parasite-infected red cells per mm3. Malaria was diagnosed more often among HbAA patients, than among other patients. Mortality rate in AA haemoglobin children was higher than 3% whereas in sickle cell trait carriers no death could be certainly attributed to malaria. The S gene rate was significantly weaker (p < 0.05) in subjects attacked by Malaria (5%) than in all other groups of children. In the endemic malaria areas the susceptibility of S gene carriers appears to be lesser than in AA haemoglobin children and could explain the paradoxically lower rate of mortality in this group.
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