Computational prediction of muscle synergy using a finite element framework for a musculoskeletal model on lower limb

Front Bioeng Biotechnol. 2023 Jul 18:11:1130219. doi: 10.3389/fbioe.2023.1130219. eCollection 2023.

Abstract

Previous studies have demonstrated that the central nervous system activates muscles in module patterns to reduce the complexity needed to control each muscle while producing a movement, which is referred to as muscle synergy. In previous musculoskeletal modeling-based muscle synergy analysis studies, as a result of simplification of the joints, a conventional rigid-body link musculoskeletal model failed to represent the physiological interactions of muscle activation and joint kinematics. However, the interaction between the muscle level and joint level that exists in vivo is an important relationship that influences the biomechanics and neurophysiology of the musculoskeletal system. In the present, a lower limb musculoskeletal model coupling a detailed representation of a joint including complex contact behavior and material representations was used for muscle synergy analysis using a decomposition method of non-negative matrix factorization (NMF). The complexity of the representation of a joint in a musculoskeletal system allows for the investigation of the physiological interactions in vivo on the musculoskeletal system, thereby facilitating the decomposition of the muscle synergy. Results indicated that, the activities of the 20 muscles on the lower limb during the stance phase of gait could be controlled by three muscle synergies, and total variance accounted for by synergies was 86.42%. The characterization of muscle synergy and musculoskeletal biomechanics is consistent with the results, thus explaining the formational mechanism of lower limb motions during gait through the reduction of the dimensions of control issues by muscle synergy and the central nervous system.

Keywords: knee; muscle activity; muscle synergy; musculoskeletal model; non-negative matrix factorization.

Grants and funding

The present research was supported in part by the Japan Society for the Promotion of Science (Grant-in-Aid for Scientific Research on Innovative Areas 19H05728) (No. 40512869; Funder ID: 10.13039/501100001691) and by the Japan Society for the Promotion of Science (Grant-in-Aid for Research Activity Start-up 22K20503) (No. 20964076; Funder ID: 10.13039/501100001691).