Related Experiment Video
Updated: Mar 12, 2026

Optimized Griess Reaction for UV-Vis and Naked-eye Determination of Anti-malarial Primaquine
Published on: October 11, 2019
Does antimalarial mass drug administration increase or decrease the risk of resistance?
1Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
Abstract:
All antimalarial drugs developed so far have eventually succumbed to resistance. There is a general belief that the more people that are exposed to an antimalarial drug, the more likely it is that resistance will emerge. Mass drug administration (MDA) is therefore considered a potent cause of antimalarial drug resistance. In this Personal View, I discuss the circumstances under which antimalarial MDA increases or decreases the risk of resistance. It is the total number of parasites exposed and their individual probabilities of survival and spread that determine the risk, not the number of people that contain them. In malaria-endemic areas, a substantial proportion of the community carries malaria parasites in their blood without being ill. Although many more people have asymptomatic than symptomatic malaria at any time, their parasite burdens are several orders of magnitude lower, and their host defence mechanisms are substantially more effective. Symptomatic infections with high parasite numbers are the most likely source of resistance emergence, so effective mass treatment that reduces the number of symptomatic cases of malaria and its transmission can reduce the threat of antimalarial resistance emerging and spreading in treated populations.
Insights
Mass drug administration (MDA) for malaria can reduce drug resistance by targeting symptomatic infections. Effective treatment lowers parasite numbers and transmission, mitigating resistance emergence in populations.
Area of Science:
- Malariology
- Infectious Disease Epidemiology
- Drug Resistance Studies
Background:
- Antimalarial drug resistance is a persistent challenge, leading to treatment failures.
- Mass drug administration (MDA) is often perceived as a primary driver of antimalarial drug resistance.
- Understanding the dynamics of resistance emergence is crucial for effective malaria control.
Purpose of the Study:
- To analyze the conditions under which antimalarial MDA influences the risk of drug resistance.
- To differentiate the impact of parasite burden versus population exposure on resistance.
- To inform strategies for mitigating antimalarial drug resistance.
Main Methods:
- Conceptual analysis of parasite survival and spread dynamics.
- Evaluation of asymptomatic versus symptomatic malaria infections.
- Review of factors influencing resistance emergence in malaria-endemic regions.
Main Results:
- Resistance risk is determined by the total number of parasites and their survival/spread probability, not solely by the number of people treated.
- Symptomatic malaria cases with high parasite loads are the primary source for resistance emergence.
- Asymptomatic infections, while common, harbor lower parasite burdens and are less likely to drive resistance.
Conclusions:
- Antimalarial MDA can decrease resistance risk if it effectively reduces symptomatic cases and overall transmission.
- Targeted mass treatment strategies focusing on high-parasite-burden infections are key.
- Reducing transmission through effective treatment is a viable approach to combat antimalarial drug resistance.
More Related Videos
Related Concept Videos
Therapeutic Drug Monitoring: Affecting Factors
Drug Toxicity: Risk factors
Factors Affecting Drug Response: Overview
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions
Desensitization and Tachyphylaxis
Pharmacodynamic Models: Additive and Proportional Drug Effect Model

