Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility

Several lines of evidence link glucose-6-phosphate dehydrogenase (G6PD) deficiency to protection from severe malaria. Early reports suggested most G6PD deficiency in sub-Saharan Africa was because of the 202A/376G G6PD A-allele, and recent association studies of G6PD deficiency have employed genotyp...

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Main Authors: Clark, T, Fry, A, Auburn, S, Campino, S, Diakite, M, Green, A, Richardson, A, Teo, Y, Small, K, Wilson, J, Jallow, M, Sisay-Joof, F, Pinder, M, Sabeti, P, Kwiatkowski, D, Rockett, K
Format: Journal article
Language:English
Published: Macmillan Publishers Ltd. 2009
Subjects:
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author Clark, T
Fry, A
Auburn, S
Campino, S
Diakite, M
Green, A
Richardson, A
Teo, Y
Small, K
Wilson, J
Jallow, M
Sisay-Joof, F
Pinder, M
Sabeti, P
Kwiatkowski, D
Rockett, K
author_facet Clark, T
Fry, A
Auburn, S
Campino, S
Diakite, M
Green, A
Richardson, A
Teo, Y
Small, K
Wilson, J
Jallow, M
Sisay-Joof, F
Pinder, M
Sabeti, P
Kwiatkowski, D
Rockett, K
author_sort Clark, T
collection OXFORD
description Several lines of evidence link glucose-6-phosphate dehydrogenase (G6PD) deficiency to protection from severe malaria. Early reports suggested most G6PD deficiency in sub-Saharan Africa was because of the 202A/376G G6PD A-allele, and recent association studies of G6PD deficiency have employed genotyping as a convenient way to determine enzyme status. However, further work has suggested that other G6PD deficiency alleles are relatively common in some regions of West Africa. To investigate the consequences of unrecognized allelic heterogeneity on association studies, in particular studies of G6PD deficiency and malaria, we carried out a case-control analysis of 2488 Gambian children with severe malaria and 3875 controls. No significant association was found between severe malaria and the 202A/376G G6PD A-allele when analyzed alone, but pooling 202A/376G with other deficiency alleles revealed the signal of protection (male odds ratio (OR) 0.77, 95% CI 0.62-0.95, P =0.016; female OR 0.71, 95% CI 0.56-0.89, P=-/004). We have identified the 968C mutation as the most common G6PD A-allele in The Gambia. Our results highlight some of the consequences of allelic heterogeneity, particularly the increased type 1 error. They also suggest that G6PD-deficient male hemizygotes and female heterozygotes are protected from severe malaria.
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spelling oxford-uuid:2deef271-4eee-4d89-9420-0d726f03573b2022-03-26T12:46:04ZAllelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibilityJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:2deef271-4eee-4d89-9420-0d726f03573bMalariaBiologyEnglishOxford University Research Archive - ValetMacmillan Publishers Ltd.2009Clark, TFry, AAuburn, SCampino, SDiakite, MGreen, ARichardson, ATeo, YSmall, KWilson, JJallow, MSisay-Joof, FPinder, MSabeti, PKwiatkowski, DRockett, KSeveral lines of evidence link glucose-6-phosphate dehydrogenase (G6PD) deficiency to protection from severe malaria. Early reports suggested most G6PD deficiency in sub-Saharan Africa was because of the 202A/376G G6PD A-allele, and recent association studies of G6PD deficiency have employed genotyping as a convenient way to determine enzyme status. However, further work has suggested that other G6PD deficiency alleles are relatively common in some regions of West Africa. To investigate the consequences of unrecognized allelic heterogeneity on association studies, in particular studies of G6PD deficiency and malaria, we carried out a case-control analysis of 2488 Gambian children with severe malaria and 3875 controls. No significant association was found between severe malaria and the 202A/376G G6PD A-allele when analyzed alone, but pooling 202A/376G with other deficiency alleles revealed the signal of protection (male odds ratio (OR) 0.77, 95% CI 0.62-0.95, P =0.016; female OR 0.71, 95% CI 0.56-0.89, P=-/004). We have identified the 968C mutation as the most common G6PD A-allele in The Gambia. Our results highlight some of the consequences of allelic heterogeneity, particularly the increased type 1 error. They also suggest that G6PD-deficient male hemizygotes and female heterozygotes are protected from severe malaria.
spellingShingle Malaria
Biology
Clark, T
Fry, A
Auburn, S
Campino, S
Diakite, M
Green, A
Richardson, A
Teo, Y
Small, K
Wilson, J
Jallow, M
Sisay-Joof, F
Pinder, M
Sabeti, P
Kwiatkowski, D
Rockett, K
Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title_full Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title_fullStr Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title_full_unstemmed Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title_short Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility
title_sort allelic heterogeneity of g6pd deficiency in west africa and severe malaria susceptibility
topic Malaria
Biology
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