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Decreased prevalence of Plasmodium falciparum resistance markers to amodiaquine despite its wide scale use as ACT partner drug in Zanzibar

机译:尽管恶性疟原虫耐药标记物已广泛用作桑给巴尔的ACT伙伴药物但其对阿莫地喹的耐药性降低

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摘要

BackgroundZanzibar has recently undergone a rapid decline in Plasmodium falciparum transmission following combined malaria control interventions with artemisinin-based combination therapy (ACT) and integrated vector control. Artesunate-amodiaquine (ASAQ) was implemented as first-line treatment for uncomplicated P. falciparum malaria in Zanzibar in 2003. Resistance to amodiaquine has been associated with the single nucleotide polymorphism (SNP) alleles pfcrt 76T, pfmdr1 86Y, 184Y and 1246Y. An accumulation of these SNP alleles in the parasite population over time might threaten ASAQ efficacy.The aim of this study was to assess whether prolonged use of ASAQ as first-line anti-malarial treatment selects for P. falciparum SNPs associated with resistance to the ACT partner drug amodiaquine.
机译:背景:在结合疟疾控制干预措施和基于青蒿素的联合治疗(ACT)以及综合病媒控制之后,桑给巴尔恶性疟原虫的传播迅速减少。青蒿琥酯-阿马二醌(ASAQ)于2003年在桑给巴尔被用作一例简单的恶性疟原虫疟疾的一线治疗。对阿莫地喹的抗性与单核苷酸多态性(SNP)等位基因pfcrt 76T,pfmdr1 86Y,184Y和1246Y相关。随着时间的推移,这些SNP等位基因在寄生虫种群中的积累可能会威胁ASAQ的效力。本研究的目的是评估长期使用ASAQ作为一线抗疟疾治疗是否会选择恶性疟原虫SNP与ACT耐药相关伙伴药物阿莫地喹。

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