The rostro-caudal gradient in the prefrontal cortex and its modulation by subthalamic deep brain stimulation in Parkinson's disease

• Published in: Scientific reports Vol. 11; no. 1; p. 2138
• Main Authors: Schumacher, F Konrad, Schumacher, Lena V, Amtage, Florian, Horn, Andreas, Egger, Karl, Piroth, Tobias, Weiller, Cornelius, Schelter, Björn O, Coenen, Volker A, Kaller, Christoph P
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 22.01.2021; Nature Publishing Group UK; Nature Portfolio
• Subjects: Cognitive ability; Deep brain stimulation; Electrical stimuli; Information processing; Infrared spectroscopy; Movement disorders; Neural networks; Neurodegenerative diseases; Parkinson's disease; Prefrontal cortex; Side effects; Solitary tract nucleus; Subthalamic nucleus
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-81535-7

Deep brain stimulation of the subthalamic nucleus (STN-DBS) alleviates motor symptoms in Parkinson's disease (PD) but also affects the prefrontal cortex (PFC), potentially leading to cognitive side effects. The present study tested alterations within the rostro-caudal hierarchy of neural processing in the PFC induced by STN-DBS in PD. Granger-causality analyses of fast functional near-infrared spectroscopy (fNIRS) measurements were used to infer directed functional connectivity from intrinsic PFC activity in 24 PD patients treated with STN-DBS. Functional connectivity was assessed ON stimulation, in steady-state OFF stimulation and immediately after the stimulator was switched ON again. Results revealed that STN-DBS significantly enhanced the rostro-caudal hierarchical organization of the PFC in patients who had undergone implantation early in the course of the disease, whereas it attenuated the rostro-caudal hierarchy in late-implanted patients. Most crucially, this systematic network effect of STN-DBS was reproducible in the second ON stimulation measurement. Supplemental analyses demonstrated the significance of prefrontal networks for cognitive functions in patients and matched healthy controls. These findings show that the modulation of prefrontal functional networks by STN-DBS is dependent on the disease duration before DBS implantation and suggest a neurophysiological mechanism underlying the side effects on prefrontally-guided cognitive functions observed under STN-DBS.