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Kainz, H.

Publications and source records attributed to Kainz, H..

6 recordsLinked to original sources

A Female Population-Averaged Musculoskeletal Model Outperforms Conventional Male-Based Generic Models in Simulating Female Gait

Most widely used lower-limb musculoskeletal models are derived from male anatomy and adapted to female participants solely by linear scaling, which may not capture sex-specific differences in pelvic and hip geometry. We developed a population-averaged, female lower-limb musculoskeletal model, built from MRI-based models of a cohort of 25 adult women using thin-plate-spline muscle-path mapping, bilateral symmetrisation, and wrapping-surface optimisation. We hypothesised that this average model, adapted to a new individual by standard linear scaling alone, would reproduce that individual's MRI-based model's walking biomechanics more closely than a linearly scaled generic male-based model. We also expected that this advantage would be concentrated in pelvis- and hip-dependent outputs rather than distributed evenly across all joints. Using 5-fold cross-validation, the scaled average-female model and the scaled male model were each compared against the held-out individual's MRI-based model across gait kinematics, joint moments, muscle moment arms, muscle forces/activations, and joint reaction forces. The average-female model outperformed the male model in every output category (Holm-corrected p [≤] *10-5), supporting our primary hypothesis. Consistent with our secondary hypothesis, differences were largest and most sustained for pelvis tilt, hip flexion, and gluteal/adductor moment arms and forces, and smaller for knee and ankle kinematics. Some divergence remained localised to early-stance knee kinematics and patellofemoral loading. The population-averaged female musculoskeletal model is freely available on SimTK https://simtk.org/projects/aver_fem and is recommended for studies involving female participants, particularly when pelvic and hip biomechanics are the primary outcomes.

biophysics↗

A Workflow to Create Personalised Musculoskeletal Models Based on Magnetic Resonance Images

Musculoskeletal simulations typically rely on generic models that may not accurately represent individual anatomy. While personalisation based on medical images can improve model accuracy, current approaches often require time-consuming workflows to create these models. We present a semi-automatic workflow for creating personalised musculoskeletal models based on magnetic resonance imaging (MRI) that does not require bone segmentation. Our workflow uses 3D Slicer and Python scripts employing Thin-Plate Spline transformation to map 106 homologous landmarks from generic models onto participants anatomy. Generic-scaled and MRI-based models were created for eight healthy participants, and simulations were performed using the participants 3D motion capture data. MRI-based models were compared with generic-scaled models through principal component analysis, and joint kinematics and joint contact forces were analysed between both modelling approaches. Clear geometric differences existed between model types, with MRI-based models showing wider pelvises and different femur/tibia proportions. Unlike generic models, MRI-based male and female models displayed systematic differences. Despite anatomical discrepancies, joint kinematics were similar between models of the same individual, except for pelvis tilt. Muscle moment arms were generally aligned with published data from cadaver studies. MRI-based models consistently produced higher joint contact forces with greater inter-individual variation, particularly at knee joints, compared to generic-scaled models. The proposed workflow simplifies MRI-based model creation while revealing significant sensitivity of joint contact forces to individual morphology, highlighting the importance of personalisation for biomechanical analyses. Author SummaryQuestions about healthy or pathological movement patterns in humans--critical for injury prevention, rehabilitation, and sports performance--are often explored with the help of musculoskeletal modelling. This approach uses a priori defined generic models of the human musculoskeletal system to study joint moments, muscle activation patterns and joint contact forces. Typically, a generic model is scaled to match the participants dimensions linearly, which does not allow for an accurate representation of their bone and muscle morphology. We developed a semi-automatic workflow to creating magnetic resonance imaging-based personalisation that does not require bone segmentation but closely matches individual geometry with the help of a non-linear fitting function. By comparing magnetic resonance imaging-based and generic-scaled models in eight individuals, we show systematic bias inherent to one of the most popular musculoskeletal models and demonstrate the importance of model personalisation for healthy adults. Our personalisation pipeline is openly available and easy to set up, which will facilitate musculoskeletal modelling studies based on highly personalised models in clinical and research settings, potentially improving treatment planning and biomechanical assessments in the future.

biophysics↗

Femoral bone growth predictions based on personalized multi-scale simulations: Validation and sensitivity analysis of a mechanobiological model

Musculoskeletal function is pivotal to long-term health. However, various patient groups develop torsional deformities, leading to clinical, functional problems. Understanding the interplay between movement pattern, bone loading and growth is crucial for improving the functional mobility of these patients and preserving long-term health. Multi-scale simulations in combination with a mechanobiological bone growth model have been used to estimate bone loads and predict femoral growth trends based on cross-sectional data. The lack of longitudinal data in previous studies hindered refinements of the mechanobiological model and validation of subject-specific growth predictions, thereby limiting clinical applications. This study aimed to validate the growth predictions using magnetic resonance images and motion capture data - collected longitudinally - from ten growing children. Additionally, a sensitivity analysis was conducted to refine model parameters. A linear regression model based on physical activity information, anthropometric data, and predictions from the refined mechanobiological model explained 70% of femoral anteversion development. Notably, the direction of femoral development was accurately predicted in 18 out of 20 femurs, suggesting that growth predictions could help to revolutionize treatment strategies for torsional deformities. Statements and DeclarationsThe authors have no relevant financial or non-financial interests to disclose.

pathology↗

Did Energy Costs of Walking Limit the Evolution of a Larger Human Birth Canal?

Energetic disadvantages of a wider pelvis have long been central to explanations of the small human birth canal and the relatively risky birth process, iconic for antagonistic selection in evolution. While static mechanics predict such effects, recent empirical studies question this view. By altering a generic musculoskeletal model beyond modern human variation one parameter at a time and applying predictive forward modelling of human gait, we examined how body dimensions impact locomotion efficiency and inferred selective pressures on past morphologies. Our findings confirm that a wider pelvis increases abductor muscle demands, as lever mechanics suggest. However, dynamic walking compensates via other muscles, minimizing the total transport cost. Moreover, slightly longer legs easily offset the modest energetic costs of a larger birth canal. We propose that other factors, such as pelvic floor stability, likely constrained the evolution of the human birth canal, rather than energetic disadvantages alone.

evolutionary biology↗

Trial-to-trial similarity and distinctness of muscle synergy activation coefficients increases during learning and with a higher level of movement proficiency

Muscle synergy analyses are used to increase our understanding of motor control. Spatially fixed synergy vectors coordinate multiple co-active muscles through activation commands, known as activation coefficients. To better understand motor learning, it is crucial to know how synergy recruitment varies during a learning task and different levels of movement proficiency. Within one session participants walked on a line, a beam, and learned to walk on a tightrope - tasks that represent different levels of proficiency. Muscle synergies were extracted over all conditions and the number of synergies was determined through the knee-point of the total variance accounted for (tVAF) curve. We found that the tVAF of one synergy decreased with task proficiency (line < beam < tightrope). Additionally, trial-to-trial similarity and distinctness of synergy activation coefficients increased with proficiency and after a learning process. We conclude that precise adjustment and refinement of synergy activation coefficients play a crucial role in motor learning.

neuroscience↗

Physics-based predictive simulations to explore the differential effects of motor control and musculoskeletal deficits on gait dysfunction in cerebral palsy: a retrospective case study

Model-based simulations of walking have the theoretical potential to support clinical decision making by predicting the functional outcome of treatments in terms of walking performance. Yet before using such simulations in clinical practice, their ability to identify the main treatment targets in specific patients needs to be demonstrated. In this study, we generated predictive simulations of walking with a medical imaging based neuro-musculoskeletal model of a child with cerebral palsy presenting crouch gait. We explored the influence of altered muscle-tendon properties, reduced neuromuscular control complexity, and spasticity on gait function in terms of joint kinematics, kinetics, muscle activity, and metabolic cost of transport. We modeled altered muscle-tendon properties by personalizing Hill-type muscle-tendon parameters based on data collected during functional movements, simpler neuromuscular control by reducing the number of independent muscle synergies, and spasticity through delayed muscle activity feedback from muscle force and force rate. Our simulations revealed that, in the presence of aberrant musculoskeletal geometries, altered muscle-tendon properties rather than reduced neuromuscular control complexity and spasticity were the primary cause of the crouch gait pattern observed for this child, which is in agreement with the clinical examination. These results suggest that muscle-tendon properties should be the primary target of interventions aiming to restore a more upright gait pattern for this child. This suggestion is in line with the gait analysis following muscle-tendon property and bone deformity corrections. The ability of our simulations to distinguish the contribution of different impairments on walking performance opens the door for identifying targeted treatment strategies with the aim of designing optimized interventions for neuro-musculoskeletal disorders.

bioengineering↗