Subthalamic and pallidal deep brain stimulation: are we modulating the same network?

Author:

Sobesky Leon1ORCID,Goede Lukas1,Odekerken Vincent J J2,Wang Qiang1,Li Ningfei1ORCID,Neudorfer Clemens1ORCID,Rajamani Nanditha1,Al-Fatly Bassam1ORCID,Reich Martin3,Volkmann Jens3,de Bie Rob M A2,Kühn Andrea A1,Horn Andreas145ORCID

Affiliation:

1. Movement Disorder and Neuromodulation Unit, Department of Neurology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt- Universität zu Berlin, Department of Neurology, 10117 Berlin, Germany

2. Department of Neurology, Amsterdam University Medical Center, Amsterdam, The Netherlands

3. Department of Neurology, University Clinic of Würzburg, 97080 Würzburg, Germany

4. Center for Brain Circuit Therapeutics, Department of Neurology, Brigham & Women’s Hospital, Harvard Medical School, Boston MA 02115, USA

5. MGH Neurosurgery & Center for Neurotechnology and Neurorecovery (CNTR) at MGH Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA

Abstract

Abstract The subthalamic nucleus and internal pallidum are main target sites for deep brain stimulation in Parkinson’s disease. Multiple trials that investigated subthalamic versus pallidal stimulation were unable to settle on a definitive optimal target between the two. One reason could be that the effect is mediated via a common functional network. To test this hypothesis, we calculated connectivity profiles seeding from deep brain stimulation electrodes in 94 patients that underwent subthalamic and 28 patients with pallidal treatment based on a normative connectome atlas calculated from 1000 healthy subjects. In each cohort, we calculated connectivity profiles that were associated with optimal clinical improvements. The two maps showed striking similarity and were able to cross-predict outcomes in the respective other cohort (R = 0.37 at P < 0.001; R = 0.34 at P = 0.032). Next, we calculated an agreement map, which retained regions common to both target sites. Crucially, this map was able to explain an additional amount of variance in clinical improvements of either cohort when compared to the maps calculated on each cohort alone. Finally, we tested profiles and predictive utility of connectivity maps calculated from different motor symptom subscores with a specific focus on bradykinesia and rigidity. While our study is based on retrospective data and indirect connectivity metrics, it may deliver empirical data to support the hypothesis of a largely overlapping network associated with effective deep brain stimulation in Parkinson’s disease irrespective of the specific target.

Funder

German Research Foundation

Deutsche Forschungsgemeinschaft, Emmy Noether Stipend

Deutsche Forschungsgemeinschaft

EU Joint Programme—Neurodegenerative Disease Research (JPND), Deutsches Zentrum für Luft- und Raumfahrt

Foundation for OCD Research

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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