Gametocytocidal clearance by artemether–lumefantrine versus artesunate–amodiaquine in North-Central Nigeria

D. Shwe, S. Pitmang, J. Abba, Mark Akindigh, D. Egah, S. Oguche
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Abstract

Background: The deployed artemether–lumefantrine (AL) and artesunate–amodiaquine (AA) medicines are known to be gametocytocidal. Continuous monitoring of their efficacies is imperative for malaria elimination interventions. To compare gametocytocidal clearance by AL versus AA. Materials and Methods: Data on demographics, anthropometry measures and gametocytes densities of 111 of 114 Human Immunodeficiency Virus (HIV) sero-negative children aged 6–59 months with uncomplicated Plasmodium falciparum malaria mono-infection, who participated in a drug therapeutic efficacy testing, were extracted. Patients who had severe malnutrition, other causes of common childhood fevers and use of antimalarial medicines in the preceding 1 week were excluded from the study. Study participants who met the enrolment criteria and gave written informed parental consent were randomized to receive AL or AA according to the manufacturer’s instructions. Clinical and parasitological evaluations were performed on D0, D1, D2, D3, D7, D14, D21 and D28. Analysis was restricted to 111 participants who completed the study. Results: Twelve (10.8%) patients had gametocytes on D0. Six (5.4%) study participants were in the AL treatment arm and 6 (5.4%) participants were in the AA treatment arm (P = 0.32). Gametocyte clearance time (GCT)AL was 104 h and (GCT)AA was 152 h (P = 0.44). Conclusion: AL and AA demonstrated comparable gametocytocidal activity in North-Central Nigeria. There is a need for continuous monitoring of the efficacies of these artemisinin-based combination therapies to keep track with the emergence of resistant Plasmodium gametocyte isolates in Nigeria.
尼日利亚中北部地区蒿甲醚-甲苯胺与青蒿琥酯-阿莫地喹的杀配子细胞效果比较
背景:已知已部署的蒿甲醚-甲苯芳碱(AL)和青蒿琥酯-阿莫地喹(AA)药物具有杀配子体作用。持续监测其效力对于消除疟疾的干预措施至关重要。比较AL与AA的杀配子体清除能力。材料与方法:提取114例6-59月龄单纯恶性疟原虫感染的人类免疫缺陷病毒(HIV)血清阴性儿童中111例参加药物疗效试验的人口统计学、人体测量和配子体密度数据。患有严重营养不良、其他原因的常见儿童发烧和在前一周使用抗疟疾药物的患者被排除在研究之外。符合入组标准并给予书面知情父母同意的研究参与者根据制造商的说明随机接受AL或AA。对D0、D1、D2、D3、D7、D14、D21和D28进行临床和寄生虫学评价。分析仅限于111名完成研究的参与者。结果:12例(10.8%)患者在D0时出现配子体。AL治疗组6名(5.4%),AA治疗组6名(5.4%)(P = 0.32)。配子细胞清除时间(GCT)AL为104 h, AA为152 h (P = 0.44)。结论:AL和AA在尼日利亚中北部具有相当的杀配子体活性。有必要持续监测这些以青蒿素为基础的联合疗法的疗效,以便跟踪尼日利亚出现的耐药疟原虫配子细胞分离株。
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