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African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania

X-linked Glucose-6-phosphate dehydrogenase (G6PD) A- deficiency is prevalent in sub-Saharan Africa populations, and has been associated with protection from severe malaria. Whether females and/or males are protected by G6PD deficiency is uncertain, due in part to G6PD and malaria phenotypic complexi...

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Autores principales: Manjurano, Alphaxard, Sepulveda, Nuno, Nadjm, Behzad, Mtove, George, Wangai, Hannah, Maxwell, Caroline, Olomi, Raimos, Reyburn, Hugh, Riley, Eleanor M., Drakeley, Christopher J., Clark, Taane G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335500/
https://www.ncbi.nlm.nih.gov/pubmed/25671784
http://dx.doi.org/10.1371/journal.pgen.1004960
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author Manjurano, Alphaxard
Sepulveda, Nuno
Nadjm, Behzad
Mtove, George
Wangai, Hannah
Maxwell, Caroline
Olomi, Raimos
Reyburn, Hugh
Riley, Eleanor M.
Drakeley, Christopher J.
Clark, Taane G.
author_facet Manjurano, Alphaxard
Sepulveda, Nuno
Nadjm, Behzad
Mtove, George
Wangai, Hannah
Maxwell, Caroline
Olomi, Raimos
Reyburn, Hugh
Riley, Eleanor M.
Drakeley, Christopher J.
Clark, Taane G.
author_sort Manjurano, Alphaxard
collection PubMed
description X-linked Glucose-6-phosphate dehydrogenase (G6PD) A- deficiency is prevalent in sub-Saharan Africa populations, and has been associated with protection from severe malaria. Whether females and/or males are protected by G6PD deficiency is uncertain, due in part to G6PD and malaria phenotypic complexity and misclassification. Almost all large association studies have genotyped a limited number of G6PD SNPs (e.g. G6PD202 / G6PD376), and this approach has been too blunt to capture the complete epidemiological picture. Here we have identified 68 G6PD polymorphisms and analysed 29 of these (i.e. those with a minor allele frequency greater than 1%) in 983 severe malaria cases and controls in Tanzania. We establish, across a number of SNPs including G6PD376, that only female heterozygotes are protected from severe malaria. Haplotype analysis reveals the G6PD locus to be under balancing selection, suggesting a mechanism of protection relying on alleles at modest frequency and avoiding fixation, where protection provided by G6PD deficiency against severe malaria is offset by increased risk of life-threatening complications. Our study also demonstrates that the much-needed large-scale studies of severe malaria and G6PD enzymatic function across African populations require the identification and analysis of the full repertoire of G6PD genetic markers.
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spelling pubmed-43355002015-03-04 African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania Manjurano, Alphaxard Sepulveda, Nuno Nadjm, Behzad Mtove, George Wangai, Hannah Maxwell, Caroline Olomi, Raimos Reyburn, Hugh Riley, Eleanor M. Drakeley, Christopher J. Clark, Taane G. PLoS Genet Research Article X-linked Glucose-6-phosphate dehydrogenase (G6PD) A- deficiency is prevalent in sub-Saharan Africa populations, and has been associated with protection from severe malaria. Whether females and/or males are protected by G6PD deficiency is uncertain, due in part to G6PD and malaria phenotypic complexity and misclassification. Almost all large association studies have genotyped a limited number of G6PD SNPs (e.g. G6PD202 / G6PD376), and this approach has been too blunt to capture the complete epidemiological picture. Here we have identified 68 G6PD polymorphisms and analysed 29 of these (i.e. those with a minor allele frequency greater than 1%) in 983 severe malaria cases and controls in Tanzania. We establish, across a number of SNPs including G6PD376, that only female heterozygotes are protected from severe malaria. Haplotype analysis reveals the G6PD locus to be under balancing selection, suggesting a mechanism of protection relying on alleles at modest frequency and avoiding fixation, where protection provided by G6PD deficiency against severe malaria is offset by increased risk of life-threatening complications. Our study also demonstrates that the much-needed large-scale studies of severe malaria and G6PD enzymatic function across African populations require the identification and analysis of the full repertoire of G6PD genetic markers. Public Library of Science 2015-02-11 /pmc/articles/PMC4335500/ /pubmed/25671784 http://dx.doi.org/10.1371/journal.pgen.1004960 Text en © 2015 Manjurano et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Manjurano, Alphaxard
Sepulveda, Nuno
Nadjm, Behzad
Mtove, George
Wangai, Hannah
Maxwell, Caroline
Olomi, Raimos
Reyburn, Hugh
Riley, Eleanor M.
Drakeley, Christopher J.
Clark, Taane G.
African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title_full African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title_fullStr African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title_full_unstemmed African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title_short African Glucose-6-Phosphate Dehydrogenase Alleles Associated with Protection from Severe Malaria in Heterozygous Females in Tanzania
title_sort african glucose-6-phosphate dehydrogenase alleles associated with protection from severe malaria in heterozygous females in tanzania
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335500/
https://www.ncbi.nlm.nih.gov/pubmed/25671784
http://dx.doi.org/10.1371/journal.pgen.1004960
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