Casula Elias Paolo, Stampanoni Bassi Mario, Pellicciari Maria Concetta, Ponzo Viviana, Veniero Domenica, Peppe Antonella, Brusa Livia, Stanzione Paolo, Caltagirone Carlo, Stefani Alessandro, Koch Giacomo
Non-Invasive Brain Stimulation Unit, Neurologia Clinica e Comportamentale, Fondazione Santa Lucia IRCCS, Rome, Italy.
Non-Invasive Brain Stimulation Unit, Neurologia Clinica e Comportamentale, Fondazione Santa Lucia IRCCS, Rome, Italy; Department of System Medicine, Policlinico di Tor Vergata, Rome, Italy.
Parkinsonism Relat Disord. 2017 Jan;34:31-37. doi: 10.1016/j.parkreldis.2016.10.009. Epub 2016 Oct 17.
The effects of deep brain stimulation of the subthalamic nucleus (DBS-STN) and L-dopa (LD) on cortical activity in Parkinson's disease (PD) are poorly understood.
By combining transcranial magnetic stimulation (TMS) and electroencephalography (EEG) we explored the effects of STN-DBS, either alone or in combination with L-Dopa (LD), on TMS-evoked cortical activity in a sample of implanted PD patients.
PD patients were tested in three clinical conditions: i) LD therapy with STN-DBS turned on (ON/ON condition); ii) without LD therapy with STN-DBS turned on (OFF/ON condition); iii) without LD therapy with STN-DBS turned off (OFF/OFF condition). TMS pulses were delivered over left M1 while simultaneously acquiring EEG. Eight age-matched healthy volunteers (HC) were tested as a control group.
STN-DBS enhanced early global TMS-evoked activity (∼45-80ms) and high-alpha TMS-evoked oscillations (11-13 Hz) as compared to OFF/OFF condition, independently from concomitant LD therapy. LD intake (ON/ON condition) produced a further increase of late TMS-evoked activity (∼80-130ms) and beta TMS-evoked oscillations (13-30 Hz), as compared to OFF/OFF and OFF/ON conditions, that normalized reactivity as compared to HC range of values.
Our data reveal that bilateral STN-DBS and LD therapy induce a modulation of specific cortical components and specific ranges of frequency. These findings demonstrate that STN-DBS and LD therapy may have synergistic effects on motor cortical activity.
丘脑底核深部脑刺激(DBS-STN)和左旋多巴(LD)对帕金森病(PD)皮质活动的影响尚不清楚。
通过结合经颅磁刺激(TMS)和脑电图(EEG),我们在植入的PD患者样本中探索了单独或与左旋多巴(LD)联合使用的STN-DBS对TMS诱发的皮质活动的影响。
PD患者在三种临床情况下进行测试:i)开启STN-DBS的LD治疗(开启/开启状态);ii)开启STN-DBS但不进行LD治疗(关闭/开启状态);iii)关闭STN-DBS且不进行LD治疗(关闭/关闭状态)。在经颅磁刺激左侧M1区的同时采集脑电图。八名年龄匹配的健康志愿者(HC)作为对照组进行测试。
与关闭/关闭状态相比,STN-DBS增强了早期整体TMS诱发的活动(约45-80毫秒)和高阿尔法TMS诱发的振荡(11-13赫兹),与同时进行的LD治疗无关。与关闭/关闭和关闭/开启状态相比,服用LD(开启/开启状态)使晚期TMS诱发的活动(约80-130毫秒)和贝塔TMS诱发的振荡(13-30赫兹)进一步增加,与HC值范围相比,反应性恢复正常。
我们的数据表明,双侧STN-DBS和LD治疗可诱导特定皮质成分和特定频率范围的调制。这些发现表明,STN-DBS和LD治疗可能对运动皮质活动具有协同作用。