脑岛
磁刺激
医学
随机对照试验
深部经颅磁刺激
慢性疼痛
物理疗法
物理医学与康复
帕金森病
刺激
疾病
神经科学
心理学
内科学
作者
Victor Rossetto Barboza,Gabriel Taricani Kubota,Valquíria Aparecida da Silva,Luciana Mendonça Barbosa,Débora Arnaut,Antônia Lilian de Lima Rodrigues,Ricardo Galhardoni,Egberto Reis Barbosa,André R. Brunoni,Manoel Jacobsen Teixeira,Rubens Gisbert Cury,Daniel Ciampi de Andrade
标识
DOI:10.1016/j.neucli.2024.102994
摘要
Objectives Altered somatosensory processing in the posterior insula may play a role in chronic pain development and contribute to Parkinson disease (PD)-related pain. Posterior-superior insula (PSI) repetitive transcranial magnetic stimulation (rTMS) has been demonstrated to have analgesic effects among patients with some chronic pain conditions. This study aimed at assessing the efficacy of PSI-rTMS for treating PD-related pain. Methods This was a double-blinded, randomized, sham-controlled, parallel-arm trial (NCT03504748). People with PD (PwP)-related chronic pain underwent five daily PSI-rTMS sessions for a week, followed by once weekly maintenance stimulations for seven weeks. rTMS was delivered at 10 Hz and 80% of the resting motor threshold. The primary outcome was a ≥ 30% pain intensity reduction at 8 weeks compared to baseline. Functionality, mood, cognitive, motor status, and somatosensory thresholds were also assessed. Results Twenty-five patients were enrolled. Mean age was 55.2 ± 9.5 years-old, and 56% were female. Nociceptive pain accounted for 60%, and neuropathic and nociplastic for 20% each. No significant difference was found for 30% pain reduction response rates between active (42.7%) and sham groups (14.6%, p = 0.26). Secondary clinical outcomes and sensory thresholds also did not differ significantly. In a post hoc analysis, PwP with nociceptive pain sub-type experienced more pain relief after active (85.7%) compared to sham PSI-rTMS (25%, p = 0.032). Conclusion Our preliminary results suggest that different types of PD-related pain may respond differently to treatment, and therefore people with PD may benefit from having PD-related pain well characterized in research trials and in clinical practice.
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