Canali P, Casarotto S, Rosanova M, Sferrazza-Papa G, Casali A G, Gosseries O, Massimini M, Smeraldi E, Colombo C, Benedetti F
Department of clinical neurosciences, scientific institute Ospedale San Raffaele, university Vita-Salute San Raffaele, San Raffaele Turro, 20, via Stamira d'Ancona, 20127 Milano, Italy.
Department of biomedical and clinical sciences "L. Sacco", università degli Studi di Milano, Milano, Italy.
Eur Psychiatry. 2017 Mar;41:10-15. doi: 10.1016/j.eurpsy.2016.10.005. Epub 2017 Feb 3.
When directly perturbed in healthy subjects, premotor cortical areas generate electrical oscillations in the beta range (20-40Hz). In schizophrenia, major depressive disorder and bipolar disorder (BD), these oscillations are markedly reduced, in terms of amplitude and frequency. However, it still remains unclear whether these abnormalities can be modulated over time, or if they can be still observed after treatment. Here, we employed transcranial magnetic stimulation (TMS) combined with EEG to assess the frontal oscillatory activity in eighteen BD patients before/after antidepressant treatments (sleep deprivation and light therapy), relative to nine healthy controls. In order to detect dominant frequencies, event related spectral perturbations (ERSP) were computed for each TMS/EEG session in all participants, using wavelet decomposition. The natural frequency at which the cortical circuit oscillates was calculated as the frequency value with the largest power across 300ms post-stimulus time interval. Severity of depression markedly decreased after treatment with 12 patients achieving response and nine patients achieving remission. TMS/EEG resulted in a significant activation of the beta/gamma band response (21-50Hz) in healthy controls. In patients, the main frequencies of premotor EEG responses to TMS did not significantly change before/after treatment and were always significantly lower than those of controls (11-27Hz) and comparable in patients achieving remission and in those not responding to treatment. These results suggest that the reduction of natural frequencies is a trait marker of BD, independent from the clinical status of the patients. The present findings shed light on the neurobiological underpinning of severe psychiatric disorders and demonstrate that TMS/EEG represents a unique tool to develop biomarkers in psychiatry.
在健康受试者受到直接扰动时,运动前皮质区域会产生β波段(20 - 40Hz)的电振荡。在精神分裂症、重度抑郁症和双相情感障碍(BD)中,这些振荡在幅度和频率方面均显著降低。然而,目前仍不清楚这些异常是否会随时间变化,或者在治疗后是否仍可观察到。在此,我们采用经颅磁刺激(TMS)结合脑电图(EEG)来评估18例BD患者在抗抑郁治疗(睡眠剥夺和光照疗法)前后相对于9名健康对照者的额叶振荡活动。为了检测主导频率,使用小波分解对所有参与者的每个TMS/EEG会话计算事件相关频谱扰动(ERSP)。将皮质回路振荡的固有频率计算为刺激后300毫秒时间间隔内功率最大的频率值。治疗后抑郁严重程度显著降低,12例患者有反应,9例患者缓解。TMS/EEG在健康对照者中导致β/γ波段反应(21 - 50Hz)显著激活。在患者中,运动前EEG对TMS反应的主要频率在治疗前后没有显著变化,并且始终显著低于对照者(11 - 27Hz),在缓解的患者和未对治疗有反应的患者中相当。这些结果表明,固有频率的降低是BD的一个特质标记,与患者的临床状态无关。本研究结果揭示了严重精神疾病的神经生物学基础,并证明TMS/EEG是开发精神病学生物标志物的独特工具。