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Brain stimulation and brain lesions converge on common causal circuits in neuropsychiatric disease.

Authors :
Siddiqi SH
Schaper FLWVJ
Horn A
Hsu J
Padmanabhan JL
Brodtmann A
Cash RFH
Corbetta M
Choi KS
Dougherty DD
Egorova N
Fitzgerald PB
George MS
Gozzi SA
Irmen F
Kuhn AA
Johnson KA
Naidech AM
Pascual-Leone A
Phan TG
Rouhl RPW
Taylor SF
Voss JL
Zalesky A
Grafman JH
Mayberg HS
Fox MD
Source :
Nature human behaviour [Nat Hum Behav] 2021 Dec; Vol. 5 (12), pp. 1707-1716. Date of Electronic Publication: 2021 Jul 08.
Publication Year :
2021

Abstract

Damage to specific brain circuits can cause specific neuropsychiatric symptoms. Therapeutic stimulation to these same circuits may modulate these symptoms. To determine whether these circuits converge, we studied depression severity after brain lesions (n = 461, five datasets), transcranial magnetic stimulation (n = 151, four datasets) and deep brain stimulation (n = 101, five datasets). Lesions and stimulation sites most associated with depression severity were connected to a similar brain circuit across all 14 datasets (P < 0.001). Circuits derived from lesions, deep brain stimulation and transcranial magnetic stimulation were similar (P < 0.0005), as were circuits derived from patients with major depression versus other diagnoses (P < 0.001). Connectivity to this circuit predicted out-of-sample antidepressant efficacy of transcranial magnetic stimulation and deep brain stimulation sites (P < 0.0001). In an independent analysis, 29 lesions and 95 stimulation sites converged on a distinct circuit for motor symptoms of Parkinson's disease (P < 0.05). We conclude that lesions, transcranial magnetic stimulation and DBS converge on common brain circuitry that may represent improved neurostimulation targets for depression and other disorders.<br /> (© 2021. The Author(s), under exclusive licence to Springer Nature Limited.)

Details

Language :
English
ISSN :
2397-3374
Volume :
5
Issue :
12
Database :
MEDLINE
Journal :
Nature human behaviour
Publication Type :
Academic Journal
Accession number :
34239076
Full Text :
https://doi.org/10.1038/s41562-021-01161-1