A computational model of Alzheimer's disease at the nano, micro, and macroscales

Front Neuroinform. 2024 Mar 22:18:1348113. doi: 10.3389/fninf.2024.1348113. eCollection 2024.

Abstract

Introduction: Mathematical models play a crucial role in investigating complex biological systems, enabling a comprehensive understanding of interactions among various components and facilitating in silico testing of intervention strategies. Alzheimer's disease (AD) is characterized by multifactorial causes and intricate interactions among biological entities, necessitating a personalized approach due to the lack of effective treatments. Therefore, mathematical models offer promise as indispensable tools in combating AD. However, existing models in this emerging field often suffer from limitations such as inadequate validation or a narrow focus on single proteins or pathways.

Methods: In this paper, we present a multiscale mathematical model that describes the progression of AD through a system of 19 ordinary differential equations. The equations describe the evolution of proteins (nanoscale), cell populations (microscale), and organ-level structures (macroscale) over a 50-year lifespan, as they relate to amyloid and tau accumulation, inflammation, and neuronal death.

Results: Distinguishing our model is a robust foundation in biological principles, ensuring improved justification for the included equations, and rigorous parameter justification derived from published experimental literature.

Conclusion: This model represents an essential initial step toward constructing a predictive framework, which holds significant potential for identifying effective therapeutic targets in the fight against AD.

Keywords: APOE; Alzheimer's disease; amyloid beta; complex biological systems; mathematical models; ordinary differential equations; personalized approach; tau proteins.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. ÉC was supported by student scholarships from the Institute of Mathematical Sciences and from the Consortium Pour l'Identification Précoce de la Maladie d'Alzheimer (CIMA-Q) in collaboration with the Fondation famille Lemaire. SM was supported by student scholarships from an operating grant (PJT-180465) from the Canadian Institutes for Health Research awarded to SD as primary investigator.