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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
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. |
format | Online Article Text |
id | pubmed-3999733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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