Evidence map›Paper›PMID 41170325›Full record

ArticleFrontiers in neurology2025

Unsupervised semi-automated MRI segmentation detects cortical lesion expansion in chronic traumatic brain injury.

Holly J Freeman, Alexander S Atalay, Jian Li, Evie Sobczak, Natalie Gilmore, Samuel B Snider, Brian C Healy, Holly Carrington, Enna Selmanovic, Ariel Pruyser and 9 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Holly J FreemanDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Alexander S AtalayDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Jian LiDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Evie SobczakDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Natalie GilmoreDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Samuel B SniderDepartment of Neurology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Brian C HealyMassachusetts General Hospital Biostatistics Center, Massachusetts General Hospital, Boston, MA, United States.
Holly CarringtonDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Enna SelmanovicDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Ariel PruyserDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Lisa BuraDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
David P SheppardDepartment of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA, United States.
David HuntDepartment of Neurological Surgery, University of Washington, Seattle, WA, United States.
Alan C SeifertBiomedical Engineering and Imaging Institute, Department of Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Yelena G BodienDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Jeanne M HoffmanDepartment of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA, United States.
Christine L Mac DonaldDepartment of Neurological Surgery, University of Washington, Seattle, WA, United States.
Kristen Dams-O'ConnorDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Brian L EdlowDepartment of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

Funding

University of Washington Alzheimer's Disease Research CenterP30AG066509 · NIA · UNIVERSITY OF WASHINGTON · PI Jeffrey J Iliff · 2020 to 2026
$29.0M
The Late Effects of TBI (LETBI) Study: Injury Patterns and Biological Markers of Post-Traumatic NeurodegenerationRF1NS115268 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kristen Dams-O'Connor · 2019 to 2026
$10.3M
Neuropathology of CTE and Delayed Effects of TBI: Toward In-Vivo DiagnosticsU01NS086625 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAMS-O'CONNOR, KRISTEN · 2014 to 2017
$6.1M
Clinical & biological signatures of post-traumatic neurodegeneration: Leveraging the TBI Model Systems of Care to accelerate in vivo diagnosis of the late effects of TBI (LETBI)RF1NS128961 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DAMS-O'CONNOR, KRISTEN · 2022 to 2022
$5.0M
Clinical & biological signatures of post-traumatic neurodegeneration: Leveraging the TBI Model Systems of Care to accelerate in vivo diagnosis of the late effects of TBI (LETBI)R01NS128961 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kristen Dams-O'Connor · 2025 to 2026
$3.3M
A Connectome-Based Clinical Trial Platform to Promote Early Recovery of Consciousness after Traumatic ComaDP2HD101400 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI EDLOW, BRIAN L. · 2019 to 2019
$2.5M
NIA NIH HHS P30 AG066509NICHD NIH HHS DP2 HD101400NINDS NIH HHS R01 NS128961NINDS NIH HHS RF1 NS115268NINDS NIH HHS RF1 NS128961NINDS NIH HHS U01 NS086625
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a risk factor for neurodegeneration and cognitive decline, yet the underlying pathophysiologic mechanisms are incompletely understood. This gap in knowledge is in part related to a lack of reliable and efficient methods for measuring cortical lesions in neuroimaging studies. The objective of this study was to develop a semi-automated lesion detection tool and apply it to an investigation of longitudinal changes in brain structure among individuals with chronic TBI. We identified 24 individuals with chronic moderate-to-severe TBI enrolled in the Late Effects of TBI (LETBI) study who had cortical lesions detected by T1-weighted MRI and underwent two MRI scans at least 2 years apart. Initial MRI scans were performed more than 1 year post-injury, and follow-up scans were performed a median of 3.1 (IQR = 1.7) years later. We leveraged FreeSurfer parcellations of T1-weighted MRI volumes and a recently developed super-resolution technique, SynthSR, to automate the identification of cortical lesions in this longitudinal dataset. Trained raters received the data in a randomized order and manually edited the automated lesion segmentations, yielding a final semi-automated lesion mask for each scan at each time point. Inter-rater variability was assessed in an independent cohort of 10 additional LETBI subjects with cortical lesions. The semi-automated lesion segmentations showed a high level of accuracy compared to "ground truth" lesion segmentations performed via manual segmentation by a separate blinded rater. In a longitudinal analysis of the semi-automated segmentations, lesion volume increased between the two time points with a median volume change of 4.91 (IQR = 12.95) mL (

Indexed as

cortical lesionlongitudinal MRIsegmentationsemi-automatedtraumatic brain injury

Identifiers

PMID41170325
PMCPMC12568329

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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.