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Biology subjects

Uchida, T. K.

Publications and source records attributed to Uchida, T. K..

3 recordsLinked to original sources

Synergy-informed bilevel optimization reveals joint-specific benefits for realistic exoskeleton torque prediction

Simulation-driven optimization can guide exoskeleton control design, but its utility is limited by the accuracy with which muscle coordination is predicted. Strict effort-minimization formulations predict non-physiological muscle shutdown under high exoskeleton assistance, leading to peak assistive torques that exceed values reported in human-in-the-loop experiments. We evaluated the accuracy of synergy-informed simulations at predicting assistance across four single-joint exoskeleton configurations: ankle plantarflexion, knee extension, hip flexion, and hip abduction. We implemented a bilevel optimization to predict a parameterized assistive torque that minimizes metabolic cost, with assisted muscle dynamics estimated via either effort-minimization simulations (minimizing muscle effort only) or synergy-informed simulations (minimizing muscle effort constrained to a synergy structure). We used experimental data from five unimpaired adults walking at their preferred speed and compared results descriptively between the two formulations within each subject. Assistance based on effort-minimization simulations shut down agonist muscle activations and overestimated peak assistive torque compared with experimental values. In contrast, constraining muscle controls to a synergy structure prevented non-physiological muscle shutdown and yielded assistive torques closer to those measured in human-in-the-loop experiments. This benefit was not observed equally across all assisted degrees of freedom or subjects, emerging only where no single synergy could be suppressed to unload the assisted muscles. Synergy weights can therefore be interpreted as joint-specific predictors of when simulations can reliably inform wearable robot design.

bioengineering↗

Hindmarsh-Rose neuronal network with spike-timing-dependent plasticity demonstrates coordinated reset neuromodulation

Computational models of brain structures impacted by Parkinson's disease are useful for studying pathological synchronization and exploring potential therapies. We use the Hindmarsh-Rose neuronal model to simulate synchronized activity in the subthalamic nucleus, capturing key features of the pathological rhythms observed in Parkinson's disease. Our model incorporates chemical synapses whose strengths evolve according to a spike-timing-dependent plasticity (STDP) rule. We apply coordinated reset stimulation with rapidly varying sequences (RVS CR) and examine its ability to weaken synaptic weights, thereby reducing neuronal synchrony. This stimulation technique delivers phase-shifted stimuli to distinct sites in a random sequence. We explore how stimulation frequency and the number of stimulation sites affect the efficacy of RVS CR at desynchronizing the network and observe good agreement with previous studies. We demonstrate that RVS CR efficacy is sensitive to the depression-to-potentiation ratio in the STDP rule, which may be an important parameter to tune when reconciling simulations with experimental data. Numerical simulation of neuronal networks is constrained by computational resources when models demand large networks. This work proposes a model that demonstrates similar utility with a relatively small network, enabling researchers to study pathological neuronal activity and treatments more efficiently.

neuroscience↗

Smartwatch-based prediction of single-stride and stride-to-stride gait outcomes using regression-based machine learning

2.Abstract and key termsSpatiotemporal variability during gait is linked to fall risk and could be monitored using wearable sensors. Although many users prefer wrist-worn sensors, most applications position at other sites. We developed and evaluated an application using a consumer-grade smartwatch inertial measurement unit (IMU). Young adults (N = 41) completed seven-minute conditions of treadmill gait at three different speeds. Single-stride outcomes (stride time, length, width, and speed) and spatiotemporal variability (coefficient of variation of each single-stride outcome) were recorded using an optoelectronic system, while 232 single- and multi-stride IMU metrics were recorded using an Apple Watch Series 5. These metrics were input to train linear, ridge, support vector machine (SVM), random forest, and extreme gradient boosting (xGB) models of each spatiotemporal outcome. We conducted Model x Condition ANOVAs to explore model sensitivity to speed-related responses. xGB models were best for single-stride outcomes (relative mean absolute error [% error]: 7-11%; intraclass correlation coefficient [ICC2,1]: 0.60-0.86) and SVM models were best for spatiotemporal variability (% error: 18-22%; ICC2,1 = 0.47-0.64). Spatiotemporal changes with speed were captured by these models (Condition: p < 0.00625). Results support the feasibility of monitoring multi-stride spatiotemporal parameters using a smartwatch IMU and machine learning.

bioengineering↗