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The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children

BACKGROUND: Primaquine, the only available drug effective against Plasmodium falciparum sexual stages, induces also a dose-dependent haemolysis, especially in glucose-6-phosphate dehydrogenase deficient (G6PDd) individuals. Therefore, it is important to determine the prevalence of this deficiency in...

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Autores principales: Okebe, Joseph, Amambua-Ngwa, Alfred, Parr, Jason, Nishimura, Sei, Daswani, Melissa, Takem, Ebako N, Affara, Muna, Ceesay, Serign J, Nwakanma, Davis, D’Alessandro, Umberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999733/
https://www.ncbi.nlm.nih.gov/pubmed/24742291
http://dx.doi.org/10.1186/1475-2875-13-148
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author Okebe, Joseph
Amambua-Ngwa, Alfred
Parr, Jason
Nishimura, Sei
Daswani, Melissa
Takem, Ebako N
Affara, Muna
Ceesay, Serign J
Nwakanma, Davis
D’Alessandro, Umberto
author_facet Okebe, Joseph
Amambua-Ngwa, Alfred
Parr, Jason
Nishimura, Sei
Daswani, Melissa
Takem, Ebako N
Affara, Muna
Ceesay, Serign J
Nwakanma, Davis
D’Alessandro, Umberto
author_sort Okebe, Joseph
collection PubMed
description BACKGROUND: Primaquine, the only available drug effective against Plasmodium falciparum sexual stages, induces also a dose-dependent haemolysis, especially in glucose-6-phosphate dehydrogenase deficient (G6PDd) individuals. Therefore, it is important to determine the prevalence of this deficiency in areas that would potentially benefit from its use. The prevalence of G6PD deficiency by genotype and enzyme activity was determined in healthy school children in The Gambia. METHODS: Blood samples from primary school children collected during a dry season malaria survey were screened for G6PDd and malaria infection. Genotypes for allele mutations reported in the country; 376, 202A-, 968A- and 542 were analysed while enzyme activity (phenotype) was assayed using a semi-quantitative commercial test kit. Enzyme activity values were fitted in a finite mixture model to determine the distribution and calculate a cut-off for deficiency. The association between genotype and phenotype for boys and girls as well as the association between mutant genotype and deficient phenotype was analysed. RESULTS: Samples from 1,437 children; 51% boys were analysed. The prevalence of P. falciparum malaria infection was 14%. The prevalence of the 202A-, 968 and 542 mutations was 1.8%, 2.1% and 1.0%, respectively, and higher in boys than in girls. The prevalence of G6PDd phenotype was 6.4% (92/1,437), 7.8% (57/728) in boys and 4.9% (35/709) in girls with significantly higher odds in the former (OR 1.64, 95% CI 1.05, 2.53, p = 0.026). The deficient phenotype was associated with reduced odds of malaria infection (OR 0.77, 95% CI 0.36, 1.62, p = 0.49). CONCLUSIONS: There is a weak association between genotype and phenotype estimates of G6PDd prevalence. The phenotype expression of deficiency represents combinations of mutant alleles rather than specific mutations. Genotype studies in individuals with a deficient phenotype would help identify alleles responsible for haemolysis.
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spelling pubmed-39997332014-04-26 The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children Okebe, Joseph Amambua-Ngwa, Alfred Parr, Jason Nishimura, Sei Daswani, Melissa Takem, Ebako N Affara, Muna Ceesay, Serign J Nwakanma, Davis D’Alessandro, Umberto Malar J Research BACKGROUND: Primaquine, the only available drug effective against Plasmodium falciparum sexual stages, induces also a dose-dependent haemolysis, especially in glucose-6-phosphate dehydrogenase deficient (G6PDd) individuals. Therefore, it is important to determine the prevalence of this deficiency in areas that would potentially benefit from its use. The prevalence of G6PD deficiency by genotype and enzyme activity was determined in healthy school children in The Gambia. METHODS: Blood samples from primary school children collected during a dry season malaria survey were screened for G6PDd and malaria infection. Genotypes for allele mutations reported in the country; 376, 202A-, 968A- and 542 were analysed while enzyme activity (phenotype) was assayed using a semi-quantitative commercial test kit. Enzyme activity values were fitted in a finite mixture model to determine the distribution and calculate a cut-off for deficiency. The association between genotype and phenotype for boys and girls as well as the association between mutant genotype and deficient phenotype was analysed. RESULTS: Samples from 1,437 children; 51% boys were analysed. The prevalence of P. falciparum malaria infection was 14%. The prevalence of the 202A-, 968 and 542 mutations was 1.8%, 2.1% and 1.0%, respectively, and higher in boys than in girls. The prevalence of G6PDd phenotype was 6.4% (92/1,437), 7.8% (57/728) in boys and 4.9% (35/709) in girls with significantly higher odds in the former (OR 1.64, 95% CI 1.05, 2.53, p = 0.026). The deficient phenotype was associated with reduced odds of malaria infection (OR 0.77, 95% CI 0.36, 1.62, p = 0.49). CONCLUSIONS: There is a weak association between genotype and phenotype estimates of G6PDd prevalence. The phenotype expression of deficiency represents combinations of mutant alleles rather than specific mutations. Genotype studies in individuals with a deficient phenotype would help identify alleles responsible for haemolysis. BioMed Central 2014-04-17 /pmc/articles/PMC3999733/ /pubmed/24742291 http://dx.doi.org/10.1186/1475-2875-13-148 Text en Copyright © 2014 Okebe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Okebe, Joseph
Amambua-Ngwa, Alfred
Parr, Jason
Nishimura, Sei
Daswani, Melissa
Takem, Ebako N
Affara, Muna
Ceesay, Serign J
Nwakanma, Davis
D’Alessandro, Umberto
The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title_full The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title_fullStr The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title_full_unstemmed The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title_short The prevalence of glucose-6-phosphate dehydrogenase deficiency in Gambian school children
title_sort prevalence of glucose-6-phosphate dehydrogenase deficiency in gambian school children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999733/
https://www.ncbi.nlm.nih.gov/pubmed/24742291
http://dx.doi.org/10.1186/1475-2875-13-148
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