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抗疟药耐药性:在印度尼西亚传播的简要历史。

Antimalarial Drug Resistance: A Brief History of Its Spread in Indonesia.

机构信息

Department of Parasitology Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.

AIDS, Toxoplasma, Opportunistic Disease and Malaria Research Group, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.

出版信息

Drug Des Devel Ther. 2023 Jul 5;17:1995-2010. doi: 10.2147/DDDT.S403672. eCollection 2023.

Abstract

Malaria remains to be a national and global challenge and priority, as stated in the strategic plan of the Indonesian Ministry of Health and Sustainable Development Goals. In Indonesia, it is targeted that malaria elimination can be achieved by 2030. Unfortunately, the development and spread of antimalarial resistance inflicts a significant risk to the national malaria control programs which can lead to increased malaria morbidity and mortality. In Indonesia, resistance to widely used antimalarial drugs has been reported in two human species, and . With the exception of artemisinin, resistance has surfaced towards all classes of antimalarial drugs. Initially, chloroquine, sulfadoxine-pyrimethamine, and primaquine were the most widely used antimalarial drugs. Regrettably, improper use has supported the robust spread of their resistance. Chloroquine resistance was first reported in 1974, while sulfadoxine-pyrimethamine emerged in 1979. Twenty years later, most provinces had declared treatment failures of both drugs. Molecular epidemiology suggested that variations in and genes were associated with chloroquine resistance, while and genes were correlated with sulfadoxine-pyrimethamine resistance. Additionally, and of genes appeared to be early warning sign to artemisinin resistance. Here, we reported mechanisms of antimalarial drugs and their development of resistance. This insight could provide awareness toward designing future treatment guidelines and control programs in Indonesia.

摘要

疟疾仍然是一个国家和全球的挑战和优先事项,正如印度尼西亚卫生部的战略计划和可持续发展目标所指出的那样。在印度尼西亚,目标是到 2030 年实现消除疟疾。不幸的是,抗疟药物的开发和传播给国家疟疾控制计划带来了重大风险,这可能导致疟疾发病率和死亡率的增加。在印度尼西亚,已经在两种人类物种[和]中报告了对广泛使用的抗疟药物的耐药性。除了青蒿素外,所有类别的抗疟药物都出现了耐药性。最初,氯喹、磺胺多辛-乙胺嘧啶和伯氨喹是最广泛使用的抗疟药物。遗憾的是,不当使用支持了它们的耐药性的强劲传播。1974 年首次报告了氯喹耐药性,而磺胺多辛-乙胺嘧啶耐药性则出现在 1979 年。20 年后,大多数省份宣布这两种药物的治疗失败。分子流行病学表明,和基因的变异与氯喹耐药性有关,而和基因与磺胺多辛-乙胺嘧啶耐药性有关。此外,和基因的变异似乎是青蒿素耐药性的早期预警信号。在这里,我们报告了抗疟药物的作用机制及其耐药性的发展。这一认识可以为印度尼西亚未来的治疗指南和控制计划的设计提供意识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f0f/10329833/d31a74173ebd/DDDT-17-1995-g0001.jpg

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