J Gómez-Soriano1,2, E Bravo-Esteban3,4, E Pérez-Rizo5, G Ávila-Martín2, I Galán-Arriero2, C Simón-Martinez2, J Taylor2,6,7. 1. Toledo Physiotherapy Research Group (GIFTO), Nursing and Physiotherapy School, Castilla La Mancha University, Toledo, Spain. 2. Sensorimotor Function Group, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain. 3. Neural Rehabilitation Group, Instituto Cajal, Council for Scientific Research (CSIC), Madrid, Spain. 4. Physiotherapy Faculty, Zaragoza University, Zaragoza, Spain. 5. Biomechanics Unit, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain. 6. Stoke Mandeville Spinal Research, National Spinal Injuries Centre, Buckinghamshire Healthcare Trust, NHS, Aylesbury, UK. 7. Harris Manchester College, Oxford University, Oxford, UK.
Abstract
STUDY DESIGN: Although abnormal cutaneous reflex (CR) activity has been identified during gait after incomplete spinal cord injury (SCI), this activity has not been directly compared in subjects with and without the spasticity syndrome. OBJECTIVES: Characterisation of CR activity during controlled rest and 'ramp and hold' phases of controlled plantarflexion in subjects with and without the SCI spasticity syndrome. DESIGN: Transverse descriptive study with non-parametric group analysis. SETTING: SCI rehabilitation hospital. METHODS: Tibialis Anterior (TA) reflexes were evoked by innocuous cutaneous plantar sole stimulation during rest and ramp and hold phases of plantarflexion torque in non-injured subjects (n=10) and after SCI with (n=9) and without (n=10) hypertonia and/or involuntary spasm activity. Integrated TA reflex responses were analysed as total (50-300 ms) or short (50-200 ms) and long-latency (200-300 ms) activity. RESULTS: Total and long-latency TA activity was inhibited in non-injured subjects and the SCI group without the spasticity syndrome during plantarflexion torque but not in the SCI spasticity group. Furthermore, loss of TA reflex inhibition during plantarflexion correlated with time after SCI (ρ=0.79, P=0.009). Moreover, TA reflex activity inversely correlated with maximum plantarflexion torque in the spasticity group (ρ=-0.75, P=0.02), despite similar non-reflex TA electromyographic activity during plantarflexion after SCI in subjects with (0.11, 0.08-0.13 mV) or without the spasticity syndrome (0.09, 0.07-0.12 mV). CONCLUSIONS: This reflex testing procedure supports previously published evidence for abnormal CR activity after SCI and may characterise the progressive disinhibition of TA reflex activity during controlled plantarflexion in subjects diagnosed with the spasticity syndrome.
STUDY DESIGN: Although abnormal cutaneous reflex (CR) activity has been identified during gait after incomplete spinal cord injury (SCI), this activity has not been directly compared in subjects with and without the spasticity syndrome. OBJECTIVES: Characterisation of CR activity during controlled rest and 'ramp and hold' phases of controlled plantarflexion in subjects with and without the SCI spasticity syndrome. DESIGN: Transverse descriptive study with non-parametric group analysis. SETTING: SCI rehabilitation hospital. METHODS: Tibialis Anterior (TA) reflexes were evoked by innocuous cutaneous plantar sole stimulation during rest and ramp and hold phases of plantarflexion torque in non-injured subjects (n=10) and after SCI with (n=9) and without (n=10) hypertonia and/or involuntary spasm activity. Integrated TA reflex responses were analysed as total (50-300 ms) or short (50-200 ms) and long-latency (200-300 ms) activity. RESULTS: Total and long-latency TA activity was inhibited in non-injured subjects and the SCI group without the spasticity syndrome during plantarflexion torque but not in the SCI spasticity group. Furthermore, loss of TA reflex inhibition during plantarflexion correlated with time after SCI (ρ=0.79, P=0.009). Moreover, TA reflex activity inversely correlated with maximum plantarflexion torque in the spasticity group (ρ=-0.75, P=0.02), despite similar non-reflex TA electromyographic activity during plantarflexion after SCI in subjects with (0.11, 0.08-0.13 mV) or without the spasticity syndrome (0.09, 0.07-0.12 mV). CONCLUSIONS: This reflex testing procedure supports previously published evidence for abnormal CR activity after SCI and may characterise the progressive disinhibition of TA reflex activity during controlled plantarflexion in subjects diagnosed with the spasticity syndrome.
Authors: Stefano Piazza; Diego Torricelli; Julio Gómez-Soriano; Diego Serrano-Muñoz; Gerardo Ávila-Martín; Iriana Galán-Arriero; José Luis Pons; Julian Taylor Journal: Med Biol Eng Comput Date: 2018-01-17 Impact factor: 2.602
Authors: Elisabeth Bravo-Esteban; Julian Taylor; Manuel Aleixandre; Cristina Simón-Martínez; Diego Torricelli; Jose Luis Pons; Gerardo Avila-Martín; Iriana Galán-Arriero; Julio Gómez-Soriano Journal: J Neuroeng Rehabil Date: 2017-06-15 Impact factor: 4.262
Authors: Gerardo Avila-Martin; Manuel Mata-Roig; Iriana Galán-Arriero; Julian S Taylor; Xavier Busquets; Pablo V Escribá Journal: PLoS One Date: 2017-12-15 Impact factor: 3.240