Evidence map›Paper›PMID 40480307›Full record

ArticleExperimental neurology2025

Unbiased population-based statistics to obtain pathologic burden of injury after experimental TBI.

G Smith, C Santana-Gomez, R J Staba, N G Harris

Abstract read
In one paragraph

Article in Experimental 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

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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

4 authors.

G SmithUCLA Brain Injury Research Center, Department of Neurosurgery, Geffen Medical School, USA.
C Santana-GomezDepartment of Neurology, University of California at Los Angeles, Los Angeles, CA 90095, USA.
R J StabaDepartment of Neurology, University of California at Los Angeles, Los Angeles, CA 90095, USA.
N G HarrisUCLA Brain Injury Research Center, Department of Neurosurgery, Geffen Medical School, USA; Intellectual Development and Disabilities Research Center, USA. Electronic address: ngharris@ucla.edu.

Funding

Strategy to Potentiate Rehabilitation after TBIR01NS116383 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HARRIS, NEIL · 2021 to 2025
$3.0M
Cerebral Substrate Support After Traumatic Brain InjuryR01NS104311 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PRINS, MAYUMI LYNN · 2018 to 2022
$1.7M
A mechanism for stunted map plasticity after TBIR01NS091222 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HARRIS, NEIL · 2015 to 2019
$1.7M
BLRD VA I50 BX005878NINDS NIH HHS R01 NS091222NINDS NIH HHS R01 NS104311NINDS NIH HHS R01 NS116383
6 · The paper itself

Abstract

Reproducibility of scientific data is a current concern throughout the neuroscience field. There are multiple on-going efforts to help resolve this problem. Within the preclinical neuroimaging field, the continued use of a region-of interest (ROI) type approaches combined with the well-known spatial heterogeneity of traumatic brain injury pathology is a barrier to the replicability and repeatability of data. Here we propose the conjoint use of an unbiased analysis of the whole brain after injury together with a population-based statistical analysis of sham-control brains as one approach that has been used in clinical research to help resolve this issue. The approach produces two volumes of pathology that are outside the normal range of sham brains, and can be interpreted as whole brain burden of injury. Using diffusion weighted imaging-derived scalars from a tensor analysis of data acquired from adult, male rats at 2, 9 days, 1 and 5 months after lateral fluid percussion injury (LFPI) and in shams (n = 73 and 12, respectively), we compared a data-driven, z-score mapping method to a whole brain and white matter-specific analysis, as well as an ROI-based analysis with brain regions preselected by virtue of their large group effect sizes. We show that the data-driven approach is statistically robust, providing the advantage of a large group effect size typical of a ROI analysis of mean scalar values derived from the tensor in regions of gross injury, but without the large multi-region statistical correction required for interrogating multiple brain areas, and without the potential bias inherent with using preselected ROIs. We show that the technique correctly captures the expected longitudinal time-course of the diffusion scalar volumes based on the spatial extent of the pathology and the known temporal changes in scalar values in the LFPI model.

Indexed as

BrainBrain Injuries, TraumaticNeuroimagingAnimalsDiffusion Magnetic Resonance ImagingDisease Models, AnimalMaleRandom AllocationRatsRats, Sprague-DawleyReproducibility of ResultsDiffusion imagingDWIRigorTraumatic brain injury

Identifiers

PMID40480307
PMCPMC13290101

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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.