Averna Alberto, Marceglia Sara, Arlotti Mattia, Locatelli Marco, Rampini Paolo, Priori Alberto, Bocci Tommaso
Aldo Ravelli" Research Center for Neurotechnology and Experimental Neurotherapeutics, Department of Health Sciences, University of Milan, 20142 Milan, Italy.
Department of Engineering and Architecture, University of Trieste, 34127 Trieste, Italy.
Clin Neurophysiol. 2022 Jan;133:29-38. doi: 10.1016/j.clinph.2021.10.003. Epub 2021 Oct 25.
To evaluate spectra and their correlations with clinical symptoms of local field potentials (LFP) acquired from wide- and close-spaced contacts (i.e. between contacts 0-3 or LFP03, and contacts 1-2 or LFP12 respectively) on the same DBS electrode within the subthalamus (STN) in Parkinson's disease (PD), before and after levodopa administration.
LFP12 and LFP03 were recorded from 20 PD patients. We evaluated oscillatory power, local and switched phase-amplitude coupling (l- and Sw-PAC) and correlation with motor symptoms (UPDRSIII).
Before levodopa, both LFP03 and LFP12 power in the α band inversely correlated with UPDRSIII. Differences between contacts were found in the low-frequency bands power. After levodopa, differences in UPDRSIII were associated to changes in LFP03 low-β and LFP12 HFO (high frequency oscillations, 250-350 Hz) power, while a modulation of the low-β power and an increased β-LFO (low frequency oscillations, 15-45 Hz) PAC was found only for LFP12.
This study reveals differences in spectral pattern between LFP12 and LFP03 before and after levodopa administration, as well as different correlations with PD motor symptoms.
Differences between LFP12 and LFP03 may offer an opportunity for optimizing adaptive deep brain stimulation (aDBS) protocols for PD. LFP12 can be used to detect β-HFO coupling and β power (i.e. bradykinesia), while LFP03 are optimal for low frequency oscillations (dyskinesias).
评估帕金森病(PD)患者丘脑底核(STN)同一脑深部电刺激(DBS)电极上宽间距和窄间距触点(即分别为触点0 - 3或LFP03,以及触点1 - 2或LFP12)所采集的局部场电位(LFP)的频谱及其与临床症状的相关性,以及左旋多巴给药前后的情况。
记录了20例PD患者的LFP12和LFP03。我们评估了振荡功率、局部和转换的相位 - 幅度耦合(l - 和Sw - PAC)以及与运动症状(UPDRSIII)的相关性。
左旋多巴治疗前,α波段的LFP03和LFP12功率均与UPDRSIII呈负相关。在低频段功率方面发现了触点之间的差异。左旋多巴治疗后,UPDRSIII的差异与LFP03低频β和LFP12高频振荡(HFO,250 - 350Hz)功率的变化相关,而仅在LFP12中发现了低频β功率的调制和β - 低频振荡(LFO,15 - 45Hz)PAC的增加。
本研究揭示了左旋多巴给药前后LFP12和LFP03频谱模式的差异,以及与PD运动症状的不同相关性。
LFP12和LFP03之间的差异可能为优化PD的适应性脑深部电刺激(aDBS)方案提供机会。LFP12可用于检测β - HFO耦合和β功率(即运动迟缓),而LFP03最适合检测低频振荡(异动症)。