癫痫的治疗效果:了解随时间变化的反应的数学框架。

Frontiers in network physiology Pub Date : 2024-06-26 eCollection Date: 2024-01-01 DOI:10.3389/fnetp.2024.1308501
Elanor G Harrington, Peter Kissack, John R Terry, Wessel Woldman, Leandro Junges
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引用次数: 0

摘要

癫痫是一种以反复发作为特征的神经系统疾病,全世界有超过 6500 万人患有癫痫。治疗通常从使用抗癫痫药物开始,包括单一疗法和综合疗法。如果药物治疗无效,通常会考虑采用手术、电刺激和病灶给药等侵入性更强的疗法,试图使患者摆脱癫痫发作。虽然很大一部分患者最终会从这些治疗方案中获益,但治疗反应往往会随着时间的推移而波动。人们对这些时间性变化背后的生理机制知之甚少,这使得预后成为治疗癫痫的一大挑战。在这里,我们使用癫痫发作转变的动态网络模型来了解癫痫发作倾向如何随着时间的推移而变化,这是兴奋性变化的结果。通过计算机模拟,我们探索了治疗对动态网络特性的影响与随着时间推移其脆弱性之间的关系,这种脆弱性允许癫痫发作倾向恢复到高发状态。对于小型网络,我们通过第一反式分量(FTC)的大小来说明其脆弱性。对于大型网络,我们发现网络效率、不一致性和异质性(度数方差)与网络对兴奋性增加的稳健性相关。这些结果为癫痫的治疗干预提供了一组潜在的预后标记。这些标记可用于支持个性化治疗策略的开发,最终有助于了解长期癫痫发作自由度。
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Treatment effects in epilepsy: a mathematical framework for understanding response over time.

Epilepsy is a neurological disorder characterized by recurrent seizures, affecting over 65 million people worldwide. Treatment typically commences with the use of anti-seizure medications, including both mono- and poly-therapy. Should these fail, more invasive therapies such as surgery, electrical stimulation and focal drug delivery are often considered in an attempt to render the person seizure free. Although a significant portion ultimately benefit from these treatment options, treatment responses often fluctuate over time. The physiological mechanisms underlying these temporal variations are poorly understood, making prognosis a significant challenge when treating epilepsy. Here we use a dynamic network model of seizure transition to understand how seizure propensity may vary over time as a consequence of changes in excitability. Through computer simulations, we explore the relationship between the impact of treatment on dynamic network properties and their vulnerability over time that permit a return to states of high seizure propensity. For small networks we show vulnerability can be fully characterised by the size of the first transitive component (FTC). For larger networks, we find measures of network efficiency, incoherence and heterogeneity (degree variance) correlate with robustness of networks to increasing excitability. These results provide a set of potential prognostic markers for therapeutic interventions in epilepsy. Such markers could be used to support the development of personalized treatment strategies, ultimately contributing to understanding of long-term seizure freedom.

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