Precision functional MRI mapping reveals distinct connectivity patterns for depression associated with traumatic brain injury

Author:

Siddiqi Shan H.123ORCID,Kandala Sridhar3,Hacker Carl D.4ORCID,Bouchard Heather5ORCID,Leuthardt Eric C.4,Corbetta Maurizio67,Morey Rajendra A.5ORCID,Brody David L.68ORCID

Affiliation:

1. Department of Psychiatry, Harvard Medical School, Boston, MA, USA.

2. Center for Brain Circuit Therapeutics, Brigham and Women’s Hospital, Boston, MA, USA.

3. Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.

4. Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO, USA.

5. Department of Psychiatry, Duke University School of Medicine and Durham VA Medical Center, Durham, NC, USA.

6. Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

7. Department of Neuroscience, University of Padua, Padua, Italy.

8. Center for Neuroscience and Regenerative Medicine, Uniformed Services University of the Health Sciences and National Institute of Neurological Disorders and Stroke, Rockville, MD, USA.

Abstract

Depression associated with traumatic brain injury (TBI) is believed to be clinically distinct from primary major depressive disorder (MDD) and may be less responsive to conventional treatments. Brain connectivity differences between the dorsal attention network (DAN), default mode network (DMN), and subgenual cingulate have been implicated in TBI and MDD. To characterize these distinctions, we applied precision functional mapping of brain network connectivity to resting-state functional magnetic resonance imaging data from five published patient cohorts, four discovery cohorts ( n = 93), and one replication cohort ( n = 180). We identified a distinct brain connectivity profile in TBI-associated depression that was independent of TBI, MDD, posttraumatic stress disorder (PTSD), depression severity, and cohort. TBI-associated depression was independently associated with decreased DAN–subgenual cingulate connectivity, increased DAN-DMN connectivity, and the combined effect of both. This effect was stronger when using precision functional mapping relative to group-level network maps. Our results support the possibility of a physiologically distinct “TBI affective syndrome,” which may benefit from individualized neuromodulation approaches to target its distinct neural circuitry.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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