Bayesian modelling of amyloid-beta dynamics and astrocyte influence in Alzheimer’s disease

BACKGROUND: Alzheimer's disease (AD) is a complicated neurological condition defined by the deposition of amyloid-beta (Aβ) plaques. Despite extensive research, the dynamics of Aβ growth, particularly the role of astrocytes, remain poorly understood, limiting the development of effective treatments. NEW METHOD: This study addresses this gap by introducing a Bayesian inference framework for modelling Aβ dynamics, incorporating both strong and weak astrocyte effects utilizing Alzheimer's Disease Neuroimaging Initiative (ADNI) clinical data. RESULTS: Through a combination of stochastic growth models and approximate Bayesian computation (ABC), we evaluate how astrocyte concentrations influence Aβ accumulation in different disease stages. Our findings show that higher astrocyte levels can suppress Aβ growth, while lower levels promote it, suggesting that astrocyte-targeted interventions may alter disease progression. COMPARISON WITH EXISTING METHODS: This data-driven probabilistic approach not only captures the inherent biological variability but also provides a tractable method to estimate uncertain parameters. CONCLUSIONS: The present research offers a valuable tool for therapeutic modelling and prediction in AD.

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Publication Details

Journal
Journal of Neuroscience Methods
Published
2026-05-01
DOI
https://doi.org/10.1016/j.jneumeth.2026.110785
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
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article

Bayesian modelling of amyloid-beta dynamics and astrocyte influence in Alzheimer’s disease

Hina Shaheen, Roderick Melnik
Journal of Neuroscience Methods
Alzheimer's disease research and treatments
article

Bayesian modelling of amyloid-beta dynamics and astrocyte influence in Alzheimer’s disease

Hina Shaheen, Roderick Melnik
article en

Abstract

BACKGROUND: Alzheimer's disease (AD) is a complicated neurological condition defined by the deposition of amyloid-beta (Aβ) plaques. Despite extensive research, the dynamics of Aβ growth, particularly the role of astrocytes, remain poorly understood, limiting the development of effective treatments. NEW METHOD: This study addresses this gap by introducing a Bayesian inference framework for modelling Aβ dynamics, incorporating both strong and weak astrocyte effects utilizing Alzheimer's Disease Neuroimaging Initiative (ADNI) clinical data. RESULTS: Through a combination of stochastic growth models and approximate Bayesian computation (ABC), we evaluate how astrocyte concentrations influence Aβ accumulation in different disease stages. Our findings show that higher astrocyte levels can suppress Aβ growth, while lower levels promote it, suggesting that astrocyte-targeted interventions may alter disease progression. COMPARISON WITH EXISTING METHODS: This data-driven probabilistic approach not only captures the inherent biological variability but also provides a tractable method to estimate uncertain parameters. CONCLUSIONS: The present research offers a valuable tool for therapeutic modelling and prediction in AD.

Journal of Neuroscience Methods
University of Manitoba (CA), Wilfrid Laurier University (CA)
Openalex Percentile: Top 8%
Alzheimer's disease research and treatments
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