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Assessment of glucose-6-phosphate dehydrogenase activity using CareStart G6PD rapid diagnostic test and associated genetic variants in Plasmodium vivax malaria endemic setting in Mauritania.
Djigo, Oum Kelthoum Mamadou; Bollahi, Mohamed Abdallahi; Hasni Ebou, Moina; Ould Ahmedou Salem, Mohamed Salem; Tahar, Rachida; Bogreau, Hervé; Basco, Leonardo; Ould Mohamed Salem Boukhary, Ali.
Afiliación
  • Djigo OKM; Unité de recherche Génomes et Milieux, Faculté des Sciences et Techniques, Université de Nouakchott Al-Aasriya, Nouveau Campus Universitaire, Nouakchott, Mauritania.
  • Bollahi MA; Centre National de Transfusion Sanguine, Ministère de la Santé, Nouakchott, Mauritania.
  • Hasni Ebou M; Unité de recherche Génomes et Milieux, Faculté des Sciences et Techniques, Université de Nouakchott Al-Aasriya, Nouveau Campus Universitaire, Nouakchott, Mauritania.
  • Ould Ahmedou Salem MS; Unité de recherche Génomes et Milieux, Faculté des Sciences et Techniques, Université de Nouakchott Al-Aasriya, Nouveau Campus Universitaire, Nouakchott, Mauritania.
  • Tahar R; UMR 216 MERIT, IRD, Faculté de Pharmacie, Univ. Paris Descartes, Paris, France.
  • Bogreau H; Unité de Parasitologie et d'Entomologie, Institut de Recherche Biomédicale des Armées, IHU-Méditerranée Infection, Marseille, France.
  • Basco L; Aix Marseille Univ, IRD, AP-HM, SSA, VITROME, Marseille, France.
  • Ould Mohamed Salem Boukhary A; IHU-Méditerranée Infection, Marseille, France.
PLoS One ; 14(9): e0220977, 2019.
Article en En | MEDLINE | ID: mdl-31525211
BACKGROUND: Primaquine is recommended by the World Health Organization (WHO) for radical treatment of Plasmodium vivax malaria. This drug is known to provoke acute hemolytic anemia in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency. Due to lack of data on G6PD deficiency, the use of primaquine has been limited in Africa. In the present study, G6PD deficiency was investigated in blood donors of various ethnic groups living in Nouakchott, a P. vivax endemic area in Mauritania. METHODOLOGY/PRINCIPAL FINDINGS: Venous blood samples from 443 healthy blood donors recruited at the National Transfusion Center in Nouakchott were screened for G6PD activity using the CareStart G6PD deficiency rapid diagnostic test. G6PD allelic variants were investigated using DiaPlexC G6PD genotyping kit that detects African (A-) and Mediterranean (B-) variants. Overall, 50 of 443 (11.3%) individuals (49 [11.8%] men and 1 [3.7%] woman) were phenotypically deficient. Amongst men, Black Africans had the highest prevalence of G6PD deficiency (15 of 100 [15%]) and White Moors the lowest (10 of 168, [5.9%]). The most commonly observed G6PD allelic variants among 44 tested G6PD-deficient men were the African variant A- (202A/376G) in 14 (31.8%), the Mediterranean variant B- (563T) in 13 (29.5%), and the Betica-Selma A- (376G/968C) allelic variant in 6 (13.6%). The Santamaria A- variant (376G/542T) and A variant (376G) were observed in only one and two individuals, respectively. None of the expected variants was observed in 8 (18.2%) of the tested phenotypically G6PD-deficient men. CONCLUSION: This is the first published data on G6PD deficiency in Mauritanians. The prevalence of phenotypic G6PD deficiency was relatively high (11.3%). It was mostly associated with either African or Mediterranean variants, in agreement with diverse Arab and Black African origins of the Mauritanian population.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Plasmodium vivax / Variación Genética / Malaria Vivax / Glucosafosfato Deshidrogenasa / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Mauritania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Plasmodium vivax / Variación Genética / Malaria Vivax / Glucosafosfato Deshidrogenasa / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Africa Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Mauritania