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Characterisation of the opposing effects of G6PD deficiency on cerebral malaria and severe malarial anaemia.

Geraldine M ClarkeKirk A RockettKatja KivinenChristina HubbartAnna E JeffreysKate RowlandsMuminatou JallowDavid J ConwayKalifa A BojangMargaret PinderStanley UsenFatoumatta Sisay-JoofGiorgio SirugoOusmane ToureMahamadou Ali TheraSalimata KonateSibiry SissokoAmadou NiangalyBelco PoudiougouValentina D ManganoEdith C BougoumaSodiomon B SirimaDavid ModianoLucas N Amenga-EtegoAnita GhansahKwadwo A KoramMichael D WilsonAnthony EnimilJennifer EvansOlukemi K AmoduSubulade OlaniyanTobias ApinjohRegina MugriAndre NdiCarolyne M NdilaSophie UyogaAlexander MachariaNorbert PeshuThomas N WilliamsAlphaxard ManjuranoNuno SepúlvedaTaane Gregory ClarkEleanor RileyChris DrakeleyHugh ReyburnVysaul NyirongoDavid KachalaMalcolm MolyneuxSarah J DunstanNguyen Hoan PhuNguyen Ngoc QuyenCao Quang ThaiTran Tinh HienLaurens ManningMoses LamanPeter SibaHarin KarunajeewaSteve AllenAngela AllenTimothy Me DavisPascal MichonIvo MuellerSíle F MolloySusana CampinoAngeliki KerasidouVictoria J CorneliusLee HartShivang S ShahGavin BandChris Ca SpencerTsiri AgbenyegaEric AchidiOgobara K DoumboJeremy FarrarKevin MarshTerrie TaylorDominic P Kwiatkowskinull null
Published in: eLife (2017)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is believed to confer protection against Plasmodium falciparum malaria, but the precise nature of the protective effecthas proved difficult to define as G6PD deficiency has multiple allelic variants with different effects in males and females, and it has heterogeneous effects on the clinical outcome of P. falciparum infection. Here we report an analysis of multiple allelic forms of G6PD deficiency in a large multi-centre case-control study of severe malaria, using the WHO classification of G6PD mutations to estimate each individual's level of enzyme activity from their genotype. Aggregated across all genotypes, we find that increasing levels of G6PD deficiency are associated with decreasing risk of cerebral malaria, but with increased risk of severe malarial anaemia. Models of balancing selection based on these findings indicate that an evolutionary trade-off between different clinical outcomes of P. falciparum infection could have been a major cause of the high levels of G6PD polymorphism seen in human populations.
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