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H‐coil repetitive transcranial magnetic stimulation for pain relief in patients with diabetic neuropathy

磁刺激 医学 刺激 麻醉 伤害 运动皮层 止痛药 糖尿病神经病变 交叉研究 反射 神经病理性疼痛 神经可塑性 可视模拟标度 心理学 物理医学与康复 神经科学 内科学 糖尿病 安慰剂 内分泌学 病理 受体 替代医学
作者
Emanuela Onesti,M. Gabriele,Chiara Cambieri,Marco Ceccanti,Ruggero Raccah,Giulia Di Stefano,A. Biasiotta,Andrea Truini,Abraham Zangen,Maurizio Inghilleri
出处
期刊:European Journal of Pain [Wiley]
卷期号:17 (9): 1347-1356 被引量:104
标识
DOI:10.1002/j.1532-2149.2013.00320.x
摘要

BACKGROUND: Painful neuropathy is associated with plasticity changes in the nervous system. Standard repetitive transcranial magnetic stimulation (rTMS) is a non-invasive technique used to study changes in cortical excitability and to inhibit pain perception. Deep rTMS is a newer development that allows direct activation of deeper neuronal populations, by a unique coil design termed the H-coil. This study was designed to assess whether deep rTMS applied over the motor cortical lower-limb representation relieves pain in patients with diabetic neuropathy. METHODS: Patients were randomly assigned to receive daily real or sham H-coil rTMS for 5 consecutive days. After a 5-week washout period, they crossed over to the alternative treatment for additional 5 days (according to a crossover study design). Outcome measures were changes in the visual analogue scale (VAS) for pain and in area and threshold of RIII nociceptive flexion reflex (RIII reflex). RESULTS: Of the 25 patients randomized, 23 completed the study. After real rTMS, the VAS scores decreased significantly (p=0.01), and so did RIII reflex area (p<0.01), while no significant effects in these variables were induced by the sham rTMS treatment. The rTMS-induced changes in the outcome measures disappeared about 3 weeks after stimulation. All patients tolerated stimulation well. CONCLUSIONS: Deep H-coil rTMS provides pain relief in patients with diabetic neuropathy. This innovative technique can induce a therapeutic effect on brain areas that otherwise remain difficult to target. rTMS may produce its analgesic effects, inducing motor cortex plasticity and activating descending inhibitory pain control systems.
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