Evidence map›Paper›PMID 36181425›Full record

ArticleBrain : a journal of neurology2023

Large-scale lesion symptom mapping of depression identifies brain regions for risk and resilience.

Nicholas T Trapp, Joel E Bruss, Kenneth Manzel, Jordan Grafman, Daniel Tranel, Aaron D Boes

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  8. Network localization of brain functional effects of ketamine treatment for major depression.European psychiatry : the journal of the Association of European Psychiatrists · 2026
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  13. Brain Network Signature of Autoscopic Phenomena in Humans.CNS neuroscience & therapeutics · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Nicholas T TrappDepartment of Psychiatry, University of Iowa, Iowa City, IA, USA.ORCID 0000-0003-0287-2964
Joel E BrussDepartment of Neurology, University of Iowa, Iowa City, IA, USA.
Kenneth ManzelDepartment of Neurology, University of Iowa, Iowa City, IA, USA.
Jordan GrafmanShirley Ryan AbilityLab, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Daniel TranelIowa Neuroscience Institute, University of Iowa, Iowa City, IA, USA.
Aaron D BoesDepartment of Psychiatry, University of Iowa, Iowa City, IA, USA.ORCID 0000-0002-7865-9257
University of Iowa · USNorthwestern University · US

Funding

The Neurobiology of Social Decision-Making: Social Inference and ContextP50MH094258 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI O'DOHERTY, JOHN P · 2012 to 2021
$18.6M
University of Iowa Hawkeye Intellectual and Developmental Disabilities Research Center (Hawk-IDDRC)P50HD103556 · NICHD · UNIVERSITY OF IOWA · PI EDWIN TED G. ABEL, Lane Strathearn · 2021 to 2026
$8.5M
The Iowa Neuroscience Specialty Program in Research Education (INSPIRE)T32MH019113 · NIMH · UNIVERSITY OF IOWA · PI HANNA E STEVENS, John A Wemmie · 1991 to 2026
$5.6M
Predicting Cognitive Outcomes from Stroke Based on Lesion LocationR01NS114405 · NINDS · UNIVERSITY OF IOWA · PI BOES, AARON D · 2020 to 2024
$2.1M
Investigating Network Plasticity Effects of Repetitive Brain Stimulation Following Invasive and Noninvasive Methods in HumansK23MH125145 · NIMH · UNIVERSITY OF IOWA · PI TRAPP, NICHOLAS THOMAS · 2021 to 2025
$934k
Investigating the Effects of Transcranial Magnetic Stimulation with Intracranial EEG in HumansR21MH120441 · NIMH · UNIVERSITY OF IOWA · PI BOES, AARON D, OYA, HIROYUKI · 2019 to 2020
$425k
NICHD NIH HHS P50 HD103556NIMH NIH HHS K23 MH125145NIMH NIH HHS L30 MH131226NIMH NIH HHS P50 MH094258NIMH NIH HHS R21 MH120441NIMH NIH HHS T32 MH019113NINDS NIH HHS R01 NS114405
6 · The paper itself

Abstract

Understanding neural circuits that support mood is a central goal of affective neuroscience, and improved understanding of the anatomy could inform more targeted interventions in mood disorders. Lesion studies provide a method of inferring the anatomical sites causally related to specific functions, including mood. Here, we performed a large-scale study evaluating the location of acquired, focal brain lesions in relation to symptoms of depression. Five hundred and twenty-six individuals participated in the study across two sites (356 male, average age 52.4 ± 14.5 years). Each subject had a focal brain lesion identified on structural imaging and an assessment of depression using the Beck Depression Inventory-II, both obtained in the chronic period post-lesion (>3 months). Multivariate lesion-symptom mapping was performed to identify lesion sites associated with higher or lower depression symptom burden, which we refer to as 'risk' versus 'resilience' regions. The brain networks and white matter tracts associated with peak regional findings were identified using functional and structural lesion network mapping, respectively. Lesion-symptom mapping identified brain regions significantly associated with both higher and lower depression severity (r = 0.11; P = 0.01). Peak 'risk' regions include the bilateral anterior insula, bilateral dorsolateral prefrontal cortex and left dorsomedial prefrontal cortex. Functional lesion network mapping demonstrated that these 'risk' regions localized to nodes of the salience network. Peak 'resilience' regions include the right orbitofrontal cortex, right medial prefrontal cortex and right inferolateral temporal cortex, nodes of the default mode network. Structural lesion network mapping implicated dorsal prefrontal white matter tracts as 'risk' tracts and ventral prefrontal white matter tracts as 'resilience' tracts, although the structural lesion network mapping findings did not survive correction for multiple comparisons. Taken together, these results demonstrate that lesions to specific nodes of the salience network and default mode network are associated with greater risk versus resiliency for depression symptoms in the setting of focal brain lesions.

Indexed as

Brain MappingDepressionAdultAgedBrainHumansMagnetic Resonance ImagingMaleMiddle AgedPrefrontal Cortexaffective neurosciencedepressionlesion–network mappinglesion–symptom mappingmood

Identifiers

PMID36181425
PMCPMC10319784
OpenAlexW4298326966

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.