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Saradhi, S.

Publications and source records attributed to Saradhi, S..

2 recordsLinked to original sources

Using a Deep Learning Approach for Model-based Control of Deep Brain Stimulation

Deep brain stimulation (DBS) has been developed as a treatment method for various neurological disorders, including Parkinsons disease, essential tremor and depression. Although DBS is effective, it often loses efficacy over sustained periods because a constant stimulation is applied without adapting to the patients current clinical state. In contrast, an adaptive closed-loop DBS system can offer more tailored stimulation in real-time based on a feedback biomarker. In early 2024, we developed a model-based DBS control framework that consists of three main functions: (1) a biophysically reasonable encoding model, (2) a simple decoding model, and (3) a controller. We used a polynomial fit function in the decoding model to approximate the neural-motor relationship, from DBS-induced Vim neural activity to muscle fiber electromyography (EMG). Despite promising results, the polynomial method is inaccurate in capturing the full representation of the neural-motor (EMG) function across different DBS frequencies. In this work, to capture the nonlinear intricate relationship between the neural and EMG patterns, we developed a one-dimensional convolutional neural network (1-D CNN) as a decoding model to predict the EMG signal directly from the DBS-induced Vim neural activity. The 1-D CNN network outputted a high R2 value of 0.997 which significantly outperformed the polynomial method (R2 = 0.277) and a deep learning approach based on long short-term memory (R2 = 0.296). We anticipate that our work highlights the need for a data-driven approach that can reliably map neural activities to symptomatic signals like EMG for better adjusting DBS parameters.

neuroscience↗

Model-Based Closed-Loop Control of Thalamic Deep Brain Stimulation

Closed-loop control of deep brain stimulation (DBS) is crucial for effective and automatic treatments of various neurological disorders like Parkinsons disease (PD) and essential tremor (ET). Manual (open-loop) DBS programming solely based on clinical observations relies on neurologists expertise and patients experience. The continuous stimulation in open-loop DBS may decrease battery life and cause side effects. On the contrary, a closed-loop DBS system utilizes a feedback biomarker/signal to track worsening (or improving) patients symptoms and offers several advantages compared to open-loop DBS. Existing closed-loop DBS control systems do not incorporate physiological mechanisms underlying the DBS or symptoms, for example how DBS modulates dynamics of synaptic plasticity. In this work, we proposed a computational framework for development of a model-based DBS controller where a biophysically-reasonable model can describe the relationship between DBS and neural activity, and a polynomial-based approximation can estimate the relationship between the neural and behavioral activity. A controller is utilized in our model in a quasi-real-time manner to find DBS patterns that significantly reduce the worsening of symptoms. These DBS patterns can be tested clinically by predicting the effect of DBS before delivering it to the patient. We applied this framework to the problem of finding optimal DBS frequencies for essential tremor given EMG recordings solely. Building on our recent network model of ventral intermediate nuclei (Vim), the main surgical target of the tremor, in response to DBS, we developed a biophysically-reasonable simulation in which physiological mechanisms underlying Vim-DBS are linked to symptomatic changes in EMG signals. By utilizing a PID controller, we showed that a closed-loop system can track EMG signals and adjusts the stimulation frequency of Vim-DBS so that the power of EMG in [2, 200] Hz reaches a desired target. We demonstrated that our model-based closed-loop control system of Vim-DBS finds an appropriate DBS frequency that aligns well with clinical studies. Our model-based closed-loop system is adaptable to different control targets, highlighting its potential usability for different diseases and personalized systems.

neuroscience↗