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ANGIOLELLI, M.

Publications and source records attributed to ANGIOLELLI, M..

2 recordsLinked to original sources

Data-driven gait cycle decomposition based on whole-body coordination dynamics

The study of human locomotion has long relied on descriptive frameworks of the gait cycle, which have provided essential insights into the functional phases of walking and their underlying biomechanical demands. While these models remain highly informative, they are largely based on observational analyses and may not fully capture the continuous, global coordination that characterizes human movement. The present study proposes an integrated framework to study whole-body coordination. This framework combines network theory with non-negative matrix factorization (NNMF) to treat gait as a dynamic system of coordinated joint interactions. Using three-dimensional kinematic data from 60 healthy subjects, we constructed a representation of whole-body coordination across time, named "dynamic kinectome". It was then decomposed using NNMF to extract spatial patterns of joint coordination and their corresponding temporal activations, allowing for an interpretable characterization of locomotor organization while preserving physiological meaning. Our analysis extracted six robust, highly consistent, and symmetrical coordination patterns across participants, effectively capturing the primary functional subtasks of locomotion. Rather than challenging classical phase descriptions, these findings enrich them by showing how coordination emerges as a continuous, often proactive process that can extend across conventional phase boundaries and systematically integrates the upper limbs for dynamic stability. Overall, this study provides a holistic, data-driven perspective on human locomotion, offering a promising basis for future investigations in motor control and may contribute to the development of sensitive biomarkers for clinical and rehabilitative applications.

bioengineering↗

Modularity-dependent storage of dynamic spiking patterns: bridging micro- and mesoscopic representations

Biological systems rely on asynchronous and temporally overlapping dynamics, allowing for the concurrent activation of multiple processes. This principle is particularly evident in brain function, where cognitive tasks engage distributed, interacting regions rather than sequentially isolated ones. To investigate the mechanisms enabling such coordination, we study a modular spiking neural network composed of leaky integrate-and-fire neurons and governed by spike-timing-dependent plasticity (STDP). Our model stores modular spatiotemporal patterns both at the mesoscopic level (sequences of modules) and at the microscopic level (precise spike timings) and includes a parameter, , which regulates the degree of temporal overlap between modules activations. By tuning , the network transitions from sequential to overlapping regimes, ranging from synfire chain-like dynamics to fully co-activated modules. We investigate how the temporal structure influences the networks capacity to encode and selectively retrieve multiple dynamical patterns, while considering biological constraints such as the cost of long-range connectivity. Our results offer insight into how spatiotemporal coding and network organisation support robust, large-scale memory storage and replay.

neuroscience↗