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

Malaria Journal

Research

Joseph Okebe¹  Ebako N Takem¹  Sei Nishimura¹  Melissa Daswani¹  Alfred Amambua-Ngwa¹  Davis Nwakanma¹  Muna Affara¹  Serign J Ceesay¹  Umberto D’Alessandro²  Jason Parr³ 

[1] Medical Research Council Unit, Atlantic Boulevard, Fajara, The Gambia;Medical Research Council Unit, Atlantic Boulevard, Fajara, The Gambia;London school of Hygiene and Tropical Medicine, London, UK;Institute of Tropical Medicine, Antwerp, Belgium;University of Manchester, Manchester, UK;

关键词: Glucose-6-phosphate dehydrogenase deficiency;    Malaria;    Genotype;    Phenotype;    Prevalence;   

DOI  :  10.1186/1475-2875-13-148

 received in 2013-11-02, accepted in 2014-04-13,  发布年份 2014

来源: Springer

【 摘 要 】

BackgroundPrimaquine, 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.MethodsBlood 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.ResultsSamples 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).ConclusionsThere 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.

【 授权许可】

CC BY   
© Okebe et al.; licensee BioMed Central Ltd. 2014