Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2020
Transcutaneous magnetic spinal cord stimulation for freezing of gait in Parkinson's disease.
Клиническое исследованиеСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Reis Menezes Janaína, Bernhart Carra Rafael, Aline Nunes Glaucia, da Silva Simões Juliana, Jacobsen Teixeira Manoel, Paiva Duarte Kleber, Ciampi de Andrade Daniel, Barbosa Egberto Reis, Antônio Marcolin Marco, Cury Rubens Gisbert
Аннотация
Dopaminergic drugs partially alleviate gait problems in Parkinson's disease, but the effects are not sustained in the long-term. Particularly, the freezing of gait directly impacts patients' quality of life. Experimental epidural spinal cord stimulation (SCS) studies have suggested positive effects on locomotion among PD patients, but the effects of non-invasive stimulation have never been explored. Here, we investigated in a prospective, open-label, pilot study the efficacy and safety of non-invasive magnetic stimulation of the spinal cord in five patients with PD who experienced gait problems, including freezing of gait. A trial of transcutaneous magnetic SCS was performed at the level of the fifth thoracic vertebra. The primary outcome was the change in freezing of gait 7 days after stimulation. Secondary outcome measures included changes in gait speed and UPDRS part III. After non-invasive spinal cord stimulation, patients experienced a 22% improvement in freezing of gait (p = 0.040) and 17.4% improvement in the UPDRS part III (p = 0.042). Timed up and go times improved by 48.2%, although this did not reach statistical significance (p = 0.06). Patients' global impression of change was 'much improved' for four patients. Improvement in gait after stimulation was reversible, since it returned to baseline scores 4 weeks after stimulation. No severe side effects were recorded. This pilot study suggests that transcutaneous magnetic spinal cord stimulation is feasible and can potentially improve gait problems in PD, without severe adverse effects. Large scale phase II trials are needed to test this hypothesis.