Evidence map›Paper›PMID 27329317›Full record

ArticleHuman brain mapping2016

Longitudinal diffusion tensor imaging after pediatric traumatic brain injury: Impact of age at injury and time since injury on pathway integrity.

Linda Ewing-Cobbs, Chad Parker Johnson, Jenifer Juranek, Dana DeMaster, Mary Prasad, Gerardo Duque, Larry Kramer, Charles S Cox, Paul R Swank

Open access · greenAbstract read
In one paragraph

Article in Human brain mapping, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
6.5field-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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 54 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Linda Ewing-CobbsDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030. Linda.ewing-cobbs@uth.tmc.edu.
Chad Parker JohnsonDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Jenifer JuranekDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Dana DeMasterDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Mary PrasadDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Gerardo DuqueDepartments of Pediatrics, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Larry KramerDiagnostic and Interventional Radiology, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Charles S CoxPediatric Surgery, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
Paul R SwankSchool of Public Health, University of Texas Health Sciences Center at Houston, Houston, Texas, 77030.
The University of Texas Health Science Center at Houston · US

Funding

Tramatic Stress After Pediatric Injury: Neurobiological InfluencesR01NS046308 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI EWING-COBBS, LINDA · 2004 to 2015
$6.0M
NINDS NIH HHS R01 NS046308
6 · The paper itself

Abstract

Following pediatric traumatic brain injury (TBI), longitudinal diffusion tensor imaging may characterize alterations in initial recovery and subsequent trajectory of white matter development. Our primary aim examined effects of age at injury and time since injury on pathway microstructure in children ages 6-15 scanned 3 and 24 months after TBI. Microstructural values generated using tract-based spatial statistics extracted from core association, limbic, and projection pathways were analyzed using general linear mixed models. Relative to children with orthopedic injury, the TBI group had lower fractional anisotropy (FA) bilaterally in all seven pathways. In left-hemisphere association pathways, school-aged children with TBI had the lowest initial pathway integrity and showed the greatest increase in FA over time suggesting continued development despite incomplete recovery. Adolescents showed limited change in FA and radial diffusivity and had the greatest residual deficit suggesting relatively arrested development. Radial diffusivity was persistently elevated in the TBI group, implicating dysmyelination as a core contributor to chronic post-traumatic neurodegenerative changes. The secondary aim compared FA values over time in the total sample, including participants contributing either one or two scans to the analysis, to the longitudinal cases contributing two scans. For each pathway, FA values and effect sizes were very similar and indicated extremely small differences in measurement of change over time in the total and longitudinal samples. Statistical approaches incorporating missing data may reliably estimate the effects of TBI and provide increased power to identify whether pathways show neurodegeneration, arrested development, or continued growth following pediatric TBI. Hum Brain Mapp 37:3929-3945, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

AdolescentAge FactorsBrainBrain Injuries, TraumaticChildChronic DiseaseDiffusion Tensor ImagingFemaleFollow-Up StudiesHumansLeast-Squares AnalysisLinear ModelsMagnetic Resonance ImagingMaleNeural PathwaysProspective Studiesaxial diffusivitychildrenchronicdysmyelinationfractional anisotropymicrostructureneurodegenerationradial diffusivitytract-based spatial statistics

Identifiers

PMID27329317
PMCPMC5053864
OpenAlexW2473992532

What OpenQuestion holds

Textmetadata
LicenceTDM
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.