Institute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi 100000, Vietnam.
Department of Biotechnology, Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Hanoi 100000, Vietnam.
Medicina (Kaunas). 2024 Jun 20;60(6):1013. doi: 10.3390/medicina60061013.
: Malaria continues to be a significant global health challenge. The efficacy of artemisinin-based combination therapies (ACTs) has declined in many parts of the Greater Mekong Subregion, including Vietnam, due to the spread of resistant malaria strains. This study was conducted to assess the efficacy of the Dihydroartemisinin (DHA)-Piperaquine (PPQ) regimen in treating uncomplicated malaria and to conduct molecular surveillance of antimalarial drug resistance in Binh Phuoc and Dak Nong provinces. : The study included 63 uncomplicated malaria falciparum patients from therapeutic efficacy studies (TES) treated following the WHO treatment guidelines (2009). Molecular marker analysis was performed on all 63 patients. Methods encompassed Sanger sequencing for mutations and quantitative real-time PCR for the gene. : This study found a marked decrease in the efficacy of the DHA-PPQ regimen, with an increased rate of treatment failures at two study sites. Genetic analysis revealed a significant presence of mutations and amplifications, indicating emerging resistance to artemisinin and its partner drug. : The effectiveness of the standard DHA-PPQ regimen has sharply declined, with rising treatment failure rates. This decline necessitates a review and possible revision of national malaria treatment guidelines. Importantly, molecular monitoring and clinical efficacy assessments together provide a robust framework for understanding and addressing detection drug resistance in malaria.
疟疾仍然是一个重大的全球健康挑战。由于抗疟菌株的传播,大湄公河次区域的许多地方,包括越南,青蒿素为基础的联合疗法(ACTs)的疗效已经下降。本研究旨在评估二氢青蒿素(DHA)-哌喹(PPQ)方案治疗无并发症疟疾的疗效,并对平定省和得农省的抗疟药物耐药性进行分子监测。
该研究包括来自疗效研究(TES)的 63 例无并发症恶性疟原虫患者,按照世界卫生组织的治疗指南(2009 年)进行治疗。对所有 63 例患者进行分子标记物分析。方法包括突变的 Sanger 测序和基因的实时定量 PCR。
本研究发现,DHA-PPQ 方案的疗效明显下降,两个研究地点的治疗失败率增加。遗传分析显示,存在明显的突变和扩增,表明对青蒿素及其联合用药出现了耐药性。
标准的 DHA-PPQ 方案的有效性急剧下降,治疗失败率上升。这一下降需要对国家疟疾治疗指南进行审查和可能的修订。重要的是,分子监测和临床疗效评估共同为了解和应对疟疾中的耐药性检测提供了一个强有力的框架。