Back to Search Start Over

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

Authors :
Geraldine M Clarke
Kirk Rockett
Katja Kivinen
Christina Hubbart
Anna E Jeffreys
Kate Rowlands
Muminatou Jallow
David J Conway
Kalifa A Bojang
Margaret Pinder
Stanley Usen
Fatoumatta Sisay-Joof
Giorgio Sirugo
Ousmane Toure
Mahamadou A Thera
Salimata Konate
Sibiry Sissoko
Amadou Niangaly
Belco Poudiougou
Valentina D Mangano
Edith C Bougouma
Sodiomon B Sirima
David Modiano
Lucas N Amenga-Etego
Anita Ghansah
Kwadwo A Koram
Michael D Wilson
Anthony Enimil
Jennifer Evans
Olukemi K Amodu
Subulade Olaniyan
Tobias Apinjoh
Regina Mugri
Andre Ndi
Carolyne M Ndila
Sophie Uyoga
Alexander Macharia
Norbert Peshu
Thomas N Williams
Alphaxard Manjurano
Nuno Sepúlveda
Taane G Clark
Eleanor Riley
Chris Drakeley
Hugh Reyburn
Vysaul Nyirongo
David Kachala
Malcolm Molyneux
Sarah J Dunstan
Nguyen Hoan Phu
Nguyen Ngoc Quyen
Cao Quang Thai
Tran Tinh Hien
Laurens Manning
Moses Laman
Peter Siba
Harin Karunajeewa
Steve Allen
Angela Allen
Timothy ME Davis
Pascal Michon
Ivo Mueller
Síle F Molloy
Susana Campino
Angeliki Kerasidou
Victoria J Cornelius
Lee Hart
Shivang S Shah
Gavin Band
Chris CA Spencer
Tsiri Agbenyega
Eric Achidi
Ogobara K Doumbo
Jeremy Farrar
Kevin Marsh
Terrie Taylor
Dominic P Kwiatkowski
MalariaGEN Consortium
Source :
eLife, Vol 6 (2017)
Publication Year :
2017
Publisher :
eLife Sciences Publications Ltd, 2017.

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is believed to confer protection against Plasmodium falciparum malaria, but the precise nature of the protective effect has 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.

Details

Language :
English
ISSN :
2050084X
Volume :
6
Database :
Directory of Open Access Journals
Journal :
eLife
Publication Type :
Academic Journal
Accession number :
edsdoj.f05449c1a20b4490b6413ada919611ca
Document Type :
article
Full Text :
https://doi.org/10.7554/eLife.15085