Off-Equilibrium Fluctuation-Dissipation Theorem Paves the Way in Alzheimer's Disease Research

Gustavo A. Patow, Juan Manuel Monti, Irene Acero-Pous, Sebastian Idesis, Anira Escrichs, Yonatan Sanz Perl, Petra Ritter, Morten L Kringelbach, Gustavo Deco
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Abstract

INTRODUCTION: Alzheimer's disease (AD) is a neurodegenerative disorder characterized by progressive cognitive decline. Although traditional methods have provided insights into brain dynamics in AD, they have limitations in capturing non-equilibrium dynamics across disease stages. Recent studies suggest that dynamic functional connectivity in resting-state networks (RSNs) may serve as a biomarker for AD, but the role of deviations from dynamical equilibrium remains underexplored. OBJECTIVE: This study applies the off-equilibrium fluctuation-dissipation theorem (FDT) [Monti2024] to analyze brain dynamics in AD, aiming to compare deviations from equilibrium in healthy controls, patients with mild cognitive impairment (MCI), and those with AD. The goal is to identify potential biomarkers for early AD detection and understand disease progression's mechanisms. METHODS: We employed a model-free approach based on FDT to analyze functional magnetic resonance imaging (fMRI) data, including healthy controls, MCI patients, and AD patients. Deviations from equilibrium in resting-state brain activity were quantified using fMRI scans. In addition, we performed model-based simulations incorporating Amyloid-Beta (ABeta), tau burdens, and Generative Effective Connectivity (GEC) for each subject. RESULTS: Our findings show that deviations from equilibrium increase during the MCI stage, indicating hyperexcitability, followed by a significant decline in later stages of AD, reflecting neuronal damage. Model-based simulations incorporating ABeta and tau burdens closely replicated these dynamics, especially in AD patients, highlighting their role in disease progression. Healthy controls exhibited lower deviations, while AD patients showed the most significant disruptions in brain dynamics. DISCUSSION: The study demonstrates that the off-equilibrium FDT framework can accurately characterize brain dynamics in AD, providing a potential biomarker for early detection. The increase in non-equilibrium deviations during the MCI stage followed by their decline in AD offers a mechanistic explanation for disease progression. Future research should explore how combining this framework with other dynamic brain measures could further refine diagnostic tools and therapeutic strategies for AD and other neurodegenerative diseases.
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非平衡波动-消散定理为阿尔茨海默病研究铺平道路
简介:阿尔茨海默病(AD)是一种神经退行性疾病,其特征是认知能力逐渐下降。虽然传统方法可以深入了解阿尔茨海默病的大脑动态变化,但在捕捉疾病不同阶段的非平衡动态变化方面存在局限性。最近的研究表明,静息态网络(RSN)中的动态功能连通性可作为AD的生物标志物,但偏离动态平衡的作用仍未得到充分探索。目的:本研究应用非平衡波动-耗散定理(FDT)[Monti2024]分析AD的大脑动态,旨在比较健康对照组、轻度认知障碍(MCI)患者和AD患者偏离平衡的情况。方法:我们采用基于 FDT 的无模型方法分析功能磁共振成像(fMRI)数据,包括健康对照组、MCI 患者和 AD 患者。利用 fMRI 扫描量化静息态大脑活动的平衡偏差。结果:我们的研究结果表明,偏离平衡的情况在 MCI 阶段会增加,表明神经兴奋性过高,随后在 AD 后期会显著下降,反映出神经元损伤。基于模型的模拟结合了 ABeta 和 tau 负担,密切复制了这些动态,尤其是在 AD 患者中,突出了它们在疾病进展中的作用。健康对照组表现出较低的偏差,而注意力缺失症患者的大脑动力学则表现出最显著的破坏。讨论:该研究表明,非平衡FDT框架能准确描述注意力缺失症患者的大脑动力学特征,为早期检测提供了潜在的生物标记。非平衡偏差在 MCI 阶段增加,随后在 AD 阶段下降,这为疾病的进展提供了机理解释。未来的研究应探索如何将这一框架与其他大脑动态测量相结合,进一步完善针对AD和其他神经退行性疾病的诊断工具和治疗策略。
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