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A translational platform for prototyping closed-loop neuromodulation systems

机译:用于闭环神经调节系统原型的翻译平台

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摘要

While modulating neural activity through stimulation is an effective treatment for neurological diseases such as Parkinson's disease and essential tremor, an opportunity for improving neuromodulation therapy remains in automatically adjusting therapy to continuously optimize patient outcomes. Practical issues associated with achieving this include the paucity of human data related to disease states, poorly validated estimators of patient state, and unknown dynamic mappings of optimal stimulation parameters based on estimated states. To overcome these challenges, we present an investigational platform including: an implanted sensing and stimulation device to collect data and run automated closed-loop algorithms; an external tool to prototype classifier and control-policy algorithms; and real-time telemetry to update the implanted device firmware and monitor its state. The prototyping system was demonstrated in a chronic large animal model studying hippocampal dynamics. We used the platform to find biomarkers of the observed states and transfer functions of different stimulation amplitudes. Data showed that moderate levels of stimulation suppress hippocampal beta activity, while high levels of stimulation produce seizure-like after-discharge activity. The biomarker and transfer function observations were mapped into classifier and control-policy algorithms, which were downloaded to the implanted device to continuously titrate stimulation amplitude for the desired network effect. The platform is designed to be a flexible prototyping tool and could be used to develop improved mechanistic models and automated closed-loop systems for a variety of neurological disorders.
机译:尽管通过刺激调节神经活动是治疗帕金森氏病和原发性震颤等神经系统疾病的有效方法,但改善神经调节疗法的机会仍然存在于自动调整疗法以不断优化患者预后的过程中。与实现此目标相关的实际问题包括与疾病状态相关的人类数据的匮乏,患者状态估计的验证不充分以及基于估计状态的最佳刺激参数的未知动态映射。为了克服这些挑战,我们提出了一个研究平台,包括:植入式传感和刺激设备,用于收集数据并运行自动闭环算法;用于分类器和控制策略算法原型的外部工具;实时遥测以更新植入的设备固件并监视其状态。该原型系统在研究海马动力学的慢性大型动物模型中得到了证明。我们使用该平台查找观察到的状态的生物标志物以及不同刺激幅度的传递函数。数据显示,中等水平的刺激会抑制海马β活性,而高水平的刺激会产生癫痫样的放电后活性。将生物标记和传递函数的观察结果映射到分类器和控制策略算法中,然后将其下载到植入设备中,以连续滴定刺激幅度以获得所需的网络效果。该平台被设计为一种灵活的原型制作工具,可用于针对各种神经系统疾病开发改进的机械模型和自动闭环系统。

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