Evidence map›Paper›PMID 42388887›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Longitudinal MAP-MRI-based Assessment of Tissue Microstructural Alterations in Acute mTBI.

Mihika Gangolli, Neil J Perkins, Luca Marinelli, Peter J Basser, Alexandru V Avram

Registry-linked trialAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02556177 (Advanced MRI Applications for Mild Traumatic Brain Injury-Phase 2), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT02556177 nacompletednot on this map

Advanced MRI Applications for Mild Traumatic Brain Injury-Phase 2

TypeinterventionalSponsorGE HealthcareRan2015 to 2018Enrolled477ConditionsConcussion, Traumatic Brain InjuryArmsMRI
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Mihika GangolliSection on Quantitative Imaging and Tissue Sciences, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda MD, USA.ORCID 0000-0002-8764-4313
Neil J PerkinsSection on Quantitative Imaging and Tissue Sciences, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda MD, USA.
Luca MarinelliGlobal Research, General Electric, Niskayuna NY, USA.
Peter J BasserSection on Quantitative Imaging and Tissue Sciences, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda MD, USA.ORCID 0000-0003-4795-6088
Alexandru V AvramSection on Quantitative Imaging and Tissue Sciences, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda MD, USA.ORCID 0000-0002-0295-601X

Funding

Fundamental Studies and Applications of Tissue SciencesZIAHD008970 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BASSER, PETER J. · 2018 to 2025
$1.5M
Intramural NIH HHS ZIA HD008970
6 · The paper itself

Abstract

backgroundMild traumatic brain injury (mTBI) is a signature injury in civilian and military populations that remains invisible to detection by conventional radiological methods. Diffusion MRI has been identified as a potential clinical tool for revealing subtle microstructural alterations associated with mTBI.

objectiveThis study evaluates whether a comprehensive and powerful diffusion MRI (dMRI) technique called mean apparent propagator (MAP) MRI can detect sequelae of mTBI.

methodsWe analyzed data from 417 participants of the GE/NFL prospective mTBI study which included 143 matched controls (mean age, 21.9 ± 8.3 years; 76 women) and 274 patients with acute mTBI and GCS ≥13 (mean age, 21.9 ± 8.5 years; 131 women). All participants underwent MRI exams at up to four visits including structural high-resolution T

resultsMAP-MRI parameter values were within the expected ranges and showed relatively little variation across visits. We found no significant differences in the longitudinal trajectories of these parameters between mTBI patients and controls. At acute post-injury timepoints, RPQ-3 and RPQ-13 scores were increased in mTBI patients relative to controls, while BESS scores were not significantly different between groups. Analysis of dMRI metrics and clinical mTBI markers showed significant correspondence between MAP-MRI metrics in cortical gray matter, caudate and pallidum and BESS scores.

conclusionWe developed and tested a state-of-the-art quantitative image processing pipeline for sensitive analysis and detection of subtle tissue changes in longitudinal clinical diffusion MRI data. The absence of a significant statistical difference between populations in the dMRI parameters in this study suggests that the mTBI corresponded to acute post-injury clinical symptoms but that the injury was not severe enough to cause detectable microstructural damage/alterations, and that increased diffusion sensitization combined with improved analysis techniques may be needed. CLINICAL IMPACT: These findings suggest that acute mTBI (GCS≥13) may not be detectable with diffusion MRI.

trial registrationClinicalTrials.gov NCT02556177.

Indexed as

diffusion MRIlongitudinal studymean apparent propagatortraumatic brain injury

Identifiers

PMID42388887
PMCPMC13317626

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Registered trials

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.