Open AccessEffects of DBS on auditory and somatosensory processing in Parkinson's disease
Author(s) -
Airaksinen Katja,
Mäkelä Jyrki P.,
Taulu Samu,
Ahonen Antti,
Nurminen Jussi,
Schnitzler Alfons,
Pekkonen Eero
Publication year - 2011
Publication title -
human brain mapping
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.005
H-Index - 191
eISSN - 1097-0193
pISSN - 1065-9471
DOI - 10.1002/hbm.21096
Subject(s) - magnetoencephalography , deep brain stimulation , somatosensory system , neuroscience , subthalamic nucleus , parkinson's disease , psychology , motor symptoms , audiology , medicine , electroencephalography , disease , pathology
Motor symptoms of Parkinson's disease (PD) can be relieved by deep brain stimulation (DBS). The mechanism of action of DBS is largely unclear. Magnetoencephalography (MEG) studies on DBS patients have been unfeasible because of strong magnetic artifacts. An artifact suppression method known as spatiotemporal signal space separation (tSSS) has mainly overcome these difficulties. We wanted to clarify whether tSSS enables noninvasive measurement of the modulation of cortical activity caused by DBS. We have studied auditory and somatosensory‐evoked fields (AEFs and SEFs) of advanced PD patients with bilateral subthalamic nucleus (STN) DBS using MEG. AEFs were elicited by 1‐kHz tones and SEFs by electrical pulses to the median nerve with DBS on and off. Data could be successfully acquired and analyzed from 12 out of 16 measured patients. The motor symptoms were significantly relieved by DBS, which clearly enhanced the ipsilateral auditory N100m responses in the right hemisphere. Contralateral N100m responses and somatosensory P60m responses also had a tendency to increase when bilateral DBS was on. MEG with tSSS offers a novel and powerful tool to investigate DBS modulation of the evoked cortical activity in PD with high temporal and spatial resolution. The results suggest that STN‐DBS modulates auditory processing in advanced PD. Hum Brain Mapp, 2011. © 2010 Wiley‐Liss, Inc.