NORMAL-LOAD · NORmalize MusculoskeletAL LOadings to Avoid bony Deformities in children with cerebral palsy
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2018-03-01 → 2020-02-29
- EU contribution
- €160,800
- Participants
- 1
- Scheme
- MSCA-IF-EF-RI
Lines connect the coordinator with its partners.
Results in brief
NORmalize MusculoskeletAL LOadings to Avoid bony Deformities in children with cerebral palsy
Cerebral palsy is a collection of clinical syndromes caused by a non-progressive lesion in the immature brain. This lesion alters neural patterns of muscle activation leading to progressive deterioration of the musculoskeletal system. Muscle contractions in children with cerebral palsy cause abnormal musculoskeletal loading, which can lead to bony deformities. Femoral deformities, e.g. increased neck-shaft angle and increased anteversion angle, are very common in children with cerebral palsy and can lead to pathological gait pattern due to abnormal muscle-moment arms. These deformities are usually corrected by de-rotation osteotomies, which are severe invasive orthopedic intervention. Growing bone is extremely responsive to mechanical loading. Hence, in children early clinical interventions, which aim to normalize the loading of the musculoskeletal system, could influence bone growth and prevent the development of bony deformities. Muscle and joint contact force cannot be measured in a non-invasive way but musculoskeletal simulations based on a person’s gait pattern can be used to calculate these forces. To investigate if clinical interventions have an impact on bone growth in children with cerebral palsy, a multi-scale modelling approach was developed and used to predict femoral growth trends before and after clinical interventions. The overall objective of this project was to evaluate if early clinical interventions have the potential to alter musculoskeletal loading conditions and therefore prevent femoral deformities in children with cerebral palsy. Importance for society Cerebral palsy is the most common pediatric neurologic disorder with a prevalence of 2-3 cases per 1,000 live births in Europe and has estimated healthcare and socio-economic lifetime costs of €800,000 to €860,000 for each affected person. This project aimed to develop a workflow to calculate femoral loadings and predict femoral growth trends in children with cerebral palsy. The promising results from this project (described below) are likely to have an influence on clinical decision-making in children with cerebral palsy in the future. If early load-modifying clinical interventions can be used to reduce the number of surgical corrections, it will decrease the burden on the child as well as decrease the socio-economic costs related to the treatment of children with cerebral palsy.
Data: CORDIS, © European Union
Project objective
Muscle contractions in children with cerebral palsy (CP) cause abnormal musculoskeletal loading, which can lead to bony deformities. Deformities of the femur are commonly corrected by de-rotation osteotomies. In children, early clinical interventions, which aim to normalize the loading of the musculoskeletal system, could influence bone growth and prevent the development of bony deformities. To investigate this assumption, I will use musculoskeletal (MSK) models to calculate the loading conditions of the femur before and after Botulinum Toxin-A injections (BTI) in lower limb muscles. The obtained loading conditions will then be used as input for a mechanobiological finite element analysis (FEA) model to assess the impact of altered loading conditions on femoral bone growth. With this simulation platform, I will use the patient’s gait pattern and BTI treatment history to relate the loading conditions to the femoral deformities and compare these to the measured deformities from medical images. If BTI or similar load-modifying clinical interventions can be used to reduce the number of surgical corrections, it will decrease the burden on the child as well as decrease the socio-economic costs related to the treatment of children with CP.During my PhD at Griffith University (Australia), I compared different methods and models for clinical gait analysis and showed that MSK models can be confidentially used in children with CP. With this project, I strive to go one-step further and show that MSK loadings in combination with a mechanobiological model can be used to enhance our understanding of the impact of clinical interventions and, therefore, improve the treatment planning in children with CP. I am highly motivated to take on the challenge and acquire the new scientific and transferable skills, which will strengthen my profile for future grant proposals and increase my opportunities for a permanent position after the fellowship.
Original text from CORDIS.
Participants
- KATHOLIEKE UNIVERSITEIT LEUVEN · LeuvenCoordinatorBelgium
Links
Data: CORDIS, © European Union
