Modeling the synergistic interplay between malaria dynamics, economic growth, and transient events

Abstract

The mosquito-borne disease (malaria) imposes significant challenges on human health, healthcare systems, and economic growth/productivity. This study develops and analyzes a model to understand the interplay between malaria dynamics, economic growth, and transient events. The study uncovers varied effects of disease and economic parameters on model outcomes, highlighting the interdependence of the reproduction number (R0) on both disease and economic factors, and a reciprocal relationship where malaria diminishes economic productivity, while higher economic output is associated with reduced malaria prevalence. This emphasizes the intricate interplay between malaria dynamics and socio-economic factors. Also, the study offers insights into malaria control and underscores the significance of optimizing external aid allocation, especially favoring an even distribution strategy, with the most significant reduction observed in the equal monthly distribution strategy compared to longer distribution intervals. Furthermore, the study shows that controlling malaria in high mosquito biting areas with limited aid, low technology, inadequate treatment, or low economic investment is challenging. The model exhibits a backward bifurcation implying that sustainability of control and mitigation measures is essential even when R0 is slightly less than one. Additionally, there is a parameter regime for which long transients are feasible. Long transients are critical for predicting the behavior of dynamic systems and identifying factors influencing transitions; they reveal reservoirs of infection, vital for disease control. Policy recommendations include prioritizing sustained control measures, optimizing external aid allocation, and reducing mosquito biting for effective disease control.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

CNN acknowledges the support of the National Science Foundation (Grant Number: DMS #2151870). OP is supported by the National Science Foundation (Grant Number: DMS #2151871), and RZ and HE are supported by the National Science Foundation (Grant Number: DMS #2151872).

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I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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