“…Indeed, for particular muscles such as cBF an increase in response amplitude in some phases of the step cycle (second half of the contralateral step cycle) could be partly related to increased background EMG activity in PD subjects. This additional background activity is consistent with earlier findings since increased EMG activity patterns during parkinsonian gait have been reported for BF by several authors (Cioni et al 1997;Dietz et al 1997;Mitoma et al 2000). However, the changes in reflex amplitudes in cBF were not limited to the phases with increased background.…”
Section: Phase-dependent Increase In Cbf In Some Pd Patientssupporting
confidence: 93%
“…For example, under conditions that resemble limping, TA activity was observed during the stance phase of the more stable leg in both healthy subjects (Dietz et al 1994;Duysens et al 2004b) and patients with PD . Under stable conditions, however, there is usually no extra TA activity during the stance phase (Cioni et al 1997;Dietz et al 1981Dietz et al , 1995Dietz et al , 1997Lewis et al 2000;Mitoma et al 2000; for exceptions see Cioni et al 1997;Dietz et al 1995). This extra TA activity is not due to the slower speed since the TA does not show extra activity during the stance phase in slow gait (Den Otter et al 2004).…”
Section: Phase-dependent Increase In Cbf In Some Pd Patientsmentioning
“…Indeed, for particular muscles such as cBF an increase in response amplitude in some phases of the step cycle (second half of the contralateral step cycle) could be partly related to increased background EMG activity in PD subjects. This additional background activity is consistent with earlier findings since increased EMG activity patterns during parkinsonian gait have been reported for BF by several authors (Cioni et al 1997;Dietz et al 1997;Mitoma et al 2000). However, the changes in reflex amplitudes in cBF were not limited to the phases with increased background.…”
Section: Phase-dependent Increase In Cbf In Some Pd Patientssupporting
confidence: 93%
“…For example, under conditions that resemble limping, TA activity was observed during the stance phase of the more stable leg in both healthy subjects (Dietz et al 1994;Duysens et al 2004b) and patients with PD . Under stable conditions, however, there is usually no extra TA activity during the stance phase (Cioni et al 1997;Dietz et al 1981Dietz et al , 1995Dietz et al , 1997Lewis et al 2000;Mitoma et al 2000; for exceptions see Cioni et al 1997;Dietz et al 1995). This extra TA activity is not due to the slower speed since the TA does not show extra activity during the stance phase in slow gait (Den Otter et al 2004).…”
Section: Phase-dependent Increase In Cbf In Some Pd Patientsmentioning
Freezing of gait is a severely problem in people with Parkinson's disease. The purpose of this study was to investigate the muscle activities of adductor longus, gluteus medius, gluteus maximus, biceps femoris, rectus femoris, gastrocnemius, and tibialis anterior using Noraxon 8 channels EMG system during stop task in patients with Parkinson's disease. Seven parkinson's patients and age matched normal participants were recruited in the study. Filtered EMG signals were rectified, smoothed and integrated. To control for the altered timing and magnitude of activity, iEMG was normalized for time and peak value. The results indicated that the patients with Parkinson showed decreased gait cycle, stance phase, swing phase time, swing phase time ratio and increased stance phase time ratio than normal participants. The patients with Parkinson showed decreased gastrocnemius muscle activity time ratio, while increased tibialis anterior muscle activity time ratio than normal participants. During stance phase before stop, the patients with Parkinson showed relatively lower average and peak iEMG in anterior tibialis and gastrocnemius muscle than normal participants. During swing phase before stop, the patients with Parkinson showed relatively higher average iEMG in gastrocnemius muscle than normal participants. During stop phase, the patients with Parkinson showed relatively lower average and peak iEMG in anterior tibialis and gastrocnemius muscle than normal participants.
“…On the other hand, patients with vascular parkinsonism (VP) exhibit upright posture of the trunk and neck, stiff leg movements, short steps with frequent shuffling, slightly wide-based stance, and impaired postural reflexes that can lead to falls [4][5][6][7][8][9]. Patients with cerebellar ataxia (CA) walk with exaggerated swing of the trunk and wide-based stance; their gait cycles are slow and irregular [1,2,10]. Although gait disorder features have been defined clinically in each disease, the fundamental characteristics of various gait kinematic parameters have not yet been determined due to three methodological problems.…”
mentioning
confidence: 99%
“…However, walking with short stride, wide stance, slow speed, and prolonged double support period is the final common expression of any dysfunction of the gait control system, not the characteristic change [5,10]. Thus, in addition to these nonspecific and secondary changes, the gait cycle or the floor reaction forces, parameters that are directly determined and controlled by neural circuits, should also be examined [5,10].…”
For assessment of gait disorders, speed and stride are measured during 10m-walking test. However, changes in these two parameters are nonspecific since they are observed in various gait disorders. In addition, the10-m walking is short and reflects only one aspect of daily living and the results could be affected by emotional stress. To examine the step cycles and forces for step-in and kick off, which are directly controlled by a complex neural circuitry, during daily walking and over a long period of time, we developed a new wearing device, the portable gait rhythmogram (PGR), which monitors gait-induced accelerations for up to 70 hours. Quantitative analysis of the gait acceleration cycle and amplitude has allowed characterization of the bradykinematic features of gait disorders in patients with Parkinson's disease: 1) A decrease in amplitude of gait acceleration in the early stages of the disease, which is compensated by fast stepping. 2) Subjective motor fluctuation did not necessarily coincide with changes in gait parameters. The results suggest that the rhythms-force correlation is set by the basal ganglia, but can be modified by the cerebral cortex. Analysis of voluntary gait in daily life could enhance our understanding of the pathomechanisms of gait disorders.
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