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. 2018 Jan 22;17(1):42.
doi: 10.1186/s12936-018-2190-z.

Primaquine ineligibility in anti-relapse therapy of Plasmodium vivax malaria: the problem of G6PD deficiency and cytochrome P-450 2D6 polymorphisms

Affiliations

Primaquine ineligibility in anti-relapse therapy of Plasmodium vivax malaria: the problem of G6PD deficiency and cytochrome P-450 2D6 polymorphisms

J Kevin Baird et al. Malar J. .

Abstract

The hypnozoite reservoir of Plasmodium vivax represents both the greatest obstacle and opportunity for ultimately eradicating this species. It is silent and cannot be diagnosed until it awakens and provokes a clinical attack with attendant morbidity, risk of mortality, and opportunities for onward transmission. The only licensed drug that kills hypnozoites is primaquine, which attacks the hypnozoite reservoir but imposes serious obstacles in doing so-at hypnozoitocidal doses, it invariably causes a threatening acute haemolytic anaemia in patients having an inborn deficiency in glucose-6-phosphate dehydrogenase (G6PD), affecting about 8% of people living in malaria endemic nations. That problem excludes a large number of people from safe and effective treatment of the latent stage of vivax malaria: the G6PD deficient, pregnant or lactating women, and young infants. These groups were estimated to comprise 14.3% of populations resident in the 95 countries with endemic vivax malaria. Another important obstacle regarding primaquine in the business of killing hypnozoites is its apparent metabolism to an active metabolite exclusively via cytochrome P-450 isozyme 2D6 (CYP2D6). Natural polymorphisms of this allele create genotypes expressing impaired enzymes that occur in over 20% of people living in Southeast Asia, where more than half of P. vivax infections occur globally. Taken together, the estimated frequencies of these primaquine ineligibles due to G6PD toxicity or impaired CYP2D6 activity composed over 35% of the populations at risk of vivax malaria. Much more detailed work is needed to refine these estimates, derive probabilities of error for them, and improve their ethnographic granularity in order to inform control and elimination strategy and tactics.

Keywords: CYP2D6; Contraindications for anti-relapse therapy; G6PD deficiency; Plasmodium vivax; Primaquine therapy.

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Figures

Fig. 1
Fig. 1
Stepwise exclusions of population subsets ineligible for Plasmodium vivax radical cure by primaquine. Red boxes indicate excluded subsets, while green are eligible. AS activity score, G6PDd G6PD deficient, hemi hemizygote, hetero heterozygote, homo homozygote, PQ primaquine

References

    1. Baird JK, Maguire JD, Price RN. Diagnosis and treatment of Plasmodium vivax malaria. Adv Parasitol. 2012;80:203–270. doi: 10.1016/B978-0-12-397900-1.00004-9. - DOI - PubMed
    1. Carson PE, Flanagan CL, Ickes CE, Alving AS. Enzymatic deficiency in primaquine-sensitive erythrocytes. Science. 1956;124:484–485. doi: 10.1126/science.124.3220.484-a. - DOI - PubMed
    1. Howes RE, Piel FB, Patil AP, Nyangiri OA, Gething PW, Dewi M, et al. G6PD deficiency prevalence and estimates of affected populations in malaria endemic countries: a geostatistical model-based map. PLoS Med. 2012;9:e1001339. doi: 10.1371/journal.pmed.1001339. - DOI - PMC - PubMed
    1. Howes RE, Battle KE, Satyagraha AW, Baird JK, Hay SI. G6PD deficiency: global distribution, genetic variants and primaquine therapy. Adv Parasitol. 2013;81:133–201. doi: 10.1016/B978-0-12-407826-0.00004-7. - DOI - PubMed
    1. Institute for Health Metrics and Evaluation. Global Burden of Disease Study 2016 (GBD 2016) population estimates 1980–2016. In: Battle K, editor. Seattle, WA: IHME, University of Washington; 2017.

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