A novel method for discrimination of dynamic muscle contractions between patients with Parkinson's disease (PD) and healthy controls on the basis of surface electromyography (EMG) and acceleration measurements is presented. In this method, dynamic EMG and acceleration measurements are analyzed using nonlinear methods and wavelets. Ten parameters capturing Parkinson's disease (PD) characteristic features in the measured signals are extracted. Each parameter is computed as time-varying, and for elbow flexion and extension movements separately. For discrimination between subjects, the dimensionality of the feature vectors formed from these parameters is reduced using a principal component approach. The cluster analysis of the low-dimensional feature vectors is then performed for flexion and extension movements separately. The EMG and acceleration data measured from 49 patients with PD and 59 healthy controls are used for analysis. According to clustering results, the method could discriminate 80 % of patient extension movements from 87 % of control extension movements, and 73 % of patient flexion movements from 82 % of control flexion movements. The results show that dynamic EMG and acceleration measurements can be informative for assessing neuromuscular dysfunction in PD, and furthermore, they may help in the objective clinical assessment of the disease.
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http://dx.doi.org/10.1109/TBME.2009.2023795 | DOI Listing |
Drug Saf
January 2025
Department of Public Health Pharmacy and Management, Sefako Makgatho Health Sciences University, Pretoria, South Africa.
Introduction: The COVID-19 pandemic accelerated new vaccine development. Limited safety data necessitated robust global safety surveillance to accurately identify and promptly communicate potential safety issues. The African Union Smart Safety Surveillance (AU-3S) program established the Joint Signal Management (JSM) group to support identification of potential vaccine safety concerns in five pilot countries (Ethiopia, Ghana, Kenya, Nigeria, South Africa), accounting for approximately 35% of the African population.
View Article and Find Full Text PDFInt J Exerc Sci
December 2024
Longwood University, Farmville, Virginia, USA.
Unlabelled: To investigate the effects of differing treadmills on impact acceleration and muscle activation.
Methods: 15 males and 7 females (27.8 ± 7.
J Neuroeng Rehabil
January 2025
Department of Biomedical Engineering, Faculty of Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Background: Motion complexity is necessary for adapting to external changes, but little is known about trunk motion complexity during seated perturbation in individuals with spinal cord injury (SCI). We aimed to investigate changes following SCI in trunk segmental motion complexity across different perturbation directions and how they affect postural control ability in individuals with SCI.
Methods: A total of 17 individuals with SCI and 18 healthy controls participated in challenging sagittal-seated perturbations with hand protection.
Sci Rep
January 2025
Department of Rehabilitation, University Hospital Olomouc, Olomouc, Czech Republic.
Motor imagery (MI) is a mental simulation of a movement without its actual execution. Our study aimed to assess how MI of two modalities of gait (normal gait and much more posturally challenging slackline gait) affects muscle activity and lower body kinematics. Electromyography (biceps femoris, gastrocnemius medialis, rectus femoris and tibialis anterior muscles) as well as acceleration and angular velocity (shank, thigh and pelvis segments) data were collected in three tasks for both MI modalities of gait (rest, gait imagery before and after the real execution of gait) in quiet bipedal stance in 26 healthy young adults.
View Article and Find Full Text PDFElife
December 2024
Department of Bioengineering, Faculty of Engineering, Imperial College London, London, United Kingdom.
Movements are performed by motoneurons transforming synaptic inputs into an activation signal that controls muscle force. The control signal emerges from interactions between ionotropic and neuromodulatory inputs to motoneurons. Critically, these interactions vary across motoneuron pools and differ between muscles.
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