The impact of malaria-protective red blood cell polymorphisms on parasite biomass in children with severe <i>Plasmodium falciparum</i> malaria

Abstract Severe falciparum malaria is a major cause of preventable child mortality in sub-Saharan Africa. The sequestration of parasitized erythrocytes in the microvasculature of vital organs is a central pathophysiological feature. The plasma concentration of the parasite protein P. falciparum Histidine-Rich Protein 2 ( Pf HRP2) has diagnostic and prognostic value in severe malaria. In the current study we investigate the potential use of plasma Pf HRP2 and the sequestration index (the ratio of plasma Pf HRP2 to circulating parasites) as quantitative traits in the conduct of case-only genetic association studies of severe malaria. We demonstrate the utility of this approach using data from over 2,000 Kenyan children with severe malaria, genotyped for 14 major candidate genes that were found to be associated with protection against severe malaria in previous studies. We show that Pf HRP2 is a more informative quantitative trait than peripheral parasite density, and that polymorphisms in four major red cell genes (the β S sickle mutation in HBB , the blood group mutation O in ABO , the α-thalassaemia mutation in HBA , and the Dantu blood group mutation in GYP ) are associated with substantially lower concentrations of plasma Pf HRP2 at admission. Further, the effect sizes we observed were considerably larger than those relating to peripheral parasite density. An unexpected outlier was the rs1541255 A&gt;G polymorphism in ATP2B4 for which we saw higher plasma Pf HRP2 concentrations, lower parasite densities and a higher sequestration index. We provide testable hypotheses for how this might be explained in the context of this specific protective allele.