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Protective Effect of Sickle Cell Trait Against Malaria- Associated Mortality And Morbidity

It is well known that only in some individuals malaria episodes progress to severe life-threatening disease, while in the majority the episodes are self-limiting. This is partly because of the host genetic factors such as sickle cell gene.

Sickle cell gene is caused by a single amino acid mutation (valine instead of glutamate at the 6th position) in the beta chain of hemoglobin gene. Inheritance of this mutated gene from both parents leads to sickle cell disease and people with this disease have shorter life expectancy. On the contrary, individuals who are carriers for the sickle cell disease (with one sickle gene and one normal hemoglobin gene, also known as sickle cell trait) have some protective advantage against malaria. As a result, the frequencies of sickle cell carriers are high in malaria endemic areas.

Most of the earlier studies that have addressed the relationship between sickle cell trait and malaria were cross sectional and therefore some important data relevant to the protective effects of sickle cell trait were missing. Our birth cohort studies (Asembo Bay Cohort Project in western Kenya ) conducted in collaboration with the Kenya Medical Research Institute allowed us to investigate this issue in depth. This study allowed us to determine that sickle cell trait provides 60% protection against overall mortality and most of this protection occurs between 2-16 months of life before the on set of clinical immunity in areas with intense transmission of malaria.

Graph of survival curves ("survival function estimates") of children HbAA, HbAS or HbSS. Those who were HbAS had a slight survival advantage over HbAA, with HbSS faring the worst. Sickle cell trait confers protection against mortality between 2-16 months of life in western Kenya.

Related Sources: Protective Effects of the Sickle Cell Gene Against Malaria Morbidity and Mortality. Aidoo M, Terlouw DJ, Kolczak MS, McElroy PD, ter Kuile FO, Kariuki S, Nahlen BL, Lal AA, Udhayakumar V. Lancet 2002; 359:1311-1312.