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G6PD deficiency alleles in a malaria-endemic region in the Western Brazilian Amazon

Authors :
Susana Campino
Lynn Grignard
Ana Rita Gomes
Chris Drakeley
Lígia Antunes Gonçalves
Jamille Gregório Dombrowski
Jim F. Huggett
Rodrigo Medeiros de Souza
Laura Hinton
Jonathan Curry
Claudio Romero Farias Marinho
Sabrina Epiphanio
Natércia Regina Mendes Silva
Taane G. Clark
Source :
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual), Universidade de São Paulo (USP), instacron:USP, Malaria Journal, Malaria Journal, Vol 16, Iss 1, Pp 1-9 (2017)
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Background Plasmodium vivax parasites are the predominant cause of malaria infections in the Brazilian Amazon. Infected individuals are treated with primaquine, which can induce haemolytic anaemia in glucose-6-phosphate dehydrogenase (G6PD)-deficient individuals and may lead to severe and fatal complications. This X-linked disorder is distributed globally and is caused by allelic variants with a geographical distribution that closely reflects populations exposed historically to endemic malaria. In Brazil, few studies have reported the frequency of G6PD deficiency (G6PDd) present in malaria-endemic areas. This is particularly important, as G6PDd screening is not currently performed before primaquine treatment. The aim of this study was to determine the prevalence of G6PDd in the region of Alto do Juruá, in the Western Brazilian Amazon, an area characterized by a high prevalence of P. vivax infection. Methods Five-hundred and sixteen male volunteers were screened for G6PDd using the fluorescence spot test (Beutler test) and CareStart™ G6PD Biosensor system. Demographic and clinical-epidemiological data were acquired through an individual interview. To assess the genetic basis of G6PDd, 24 SNPs were genotyped using the Kompetitive Allele Specific PCR assay. Results Twenty-three (4.5%) individuals were G6PDd. No association was found between G6PDd and the number of malaria cases. An increased risk of reported haemolysis symptoms and blood transfusions was evident among the G6PDd individuals. Twenty-two individuals had the G6PDd A(−) variant and one the G6PD A(+) variant. The Mediterranean variant was not present. Apart from one polymorphism, almost all SNPs were monomorphic or with low frequencies (0–0.04%). No differences were detected among ethnic groups. Conclusions The data indicates that ~1/23 males from the Alto do Juruá could be G6PD deficient and at risk of haemolytic anaemia if treated with primaquine. G6PD A(−) is the most frequent deficiency allele in this population. These results concur with reported G6PDd in other regions in Brazil. Routine G6PDd screening to personalize primaquine administration should be considered, particularly as complete treatment of patients with vivax malaria using chloroquine and primaquine, is crucial for malaria elimination. Electronic supplementary material The online version of this article (doi:10.1186/s12936-017-1889-6) contains supplementary material, which is available to authorized users.

Details

ISSN :
14752875
Volume :
16
Database :
OpenAIRE
Journal :
Malaria Journal
Accession number :
edsair.doi.dedup.....33ce2faff137dd543778ce53461df0bb
Full Text :
https://doi.org/10.1186/s12936-017-1889-6