Evidence map›Paper›PMID 35467058›Full record

ArticleHuman brain mapping2022

Longitudinal white matter microstructural changes in pediatric mild traumatic brain injury: An A-CAP study.

Ashley L Ware, Keith Owen Yeates, Ken Tang, Ayushi Shukla, Adrian I Onicas, Sunny Guo, Naomi Goodrich-Hunsaker, Nishard Abdeen, Miriam H Beauchamp, Christian Beaulieu and 12 more

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 3 pooled it
4.3field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 3 syntheses or guidelines pooled it, 32 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

22 authors at 8 institutions in 3 countries.

Ashley L WareDepartment of Psychology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-8390-4915
Keith Owen YeatesDepartment of Psychology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Ken TangIndependent Statistical Consulting, Richmond, British Columbia, Canada.
Ayushi ShuklaDepartment of Radiology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Adrian I OnicasDepartment of Psychology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Sunny GuoDepartment of Psychology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Naomi Goodrich-HunsakerDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.
Nishard AbdeenDepartment of Radiology, University of Ottawa, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Miriam H BeauchampDepartment of Psychology, University of Montreal & CHU Sainte-Justine Hospital Research Center, Montréal, Québec, Canada.
Christian BeaulieuDepartment of Biomedical Engineering, University of Alberta, Edmonton, Alberta, Canada.
Bruce BjornsonDivision of Neurology, Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada; 2. BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
William CraigUniversity of Alberta and Stollery Children's Hospital, Edmonton, Alberta, Canada.
Mathieu DehaesDepartment of Radiology, Radio-oncology and Nuclear Medicine, Institute of Biomedical Engineering, University of Montreal; CHU Sainte-Justine Research Center, Montréal, Québec, Canada.
Quynh DoanDepartment of Pediatrics, University of British Columbia, BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Sylvain DeschenesCHU Sainte-Justine Research Center; Department of Radiology, Radio-oncology and Nuclear Medicine, University of Montreal, Montréal, Québec, Canada.
Stephen B FreedmanDepartment of Emergency Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Bradley G GoodyearDepartment of Radiology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Jocelyn GravelDepartment of Pediatric Emergency Medicine, Department of Pediatrics, CHU Sainte-Justine, University of Montréal, Montréal, Québec, Canada.
Andrée-Anne LedouxDepartment of Cellular and Molecular Medicine, University of Ottawa, & Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Roger ZemekDepartment of Pediatrics and Emergency Medicine, University of Ottawa, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Catherine LebelDepartment of Radiology, Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-0344-4032
Pediatric Emergency Research Canada A-CAP Study Team
University of Calgary · CACentre Hospitalier Universitaire Sainte-Justine · CAUniversity of Ottawa · CAUniversity of Alberta · CAUniversity of British Columbia · CAIMT School for Advanced Studies Lucca · ITStatistical Research (United States) · USUniversity of Utah · US

Funding

CIHR FDN143304
6 · The paper itself

Abstract

In the largest sample studied to date, white matter microstructural trajectories and their relation to persistent symptoms were examined after pediatric mild traumatic brain injury (mTBI). This prospective, longitudinal cohort study recruited children aged 8-16.99 years with mTBI or mild orthopedic injury (OI) from five pediatric emergency departments. Children's pre-injury and 1-month post-injury symptom ratings were used to classify mTBI with or without persistent symptoms. Children completed diffusion-weighted imaging at post-acute (2-33 days post-injury) and chronic (3 or 6 months via random assignment) post-injury assessments. Mean diffusivity (MD) and fractional anisotropy (FA) were derived for 18 white matter tracts in 560 children (362 mTBI/198 OI), 407 with longitudinal data. Superior longitudinal fasciculus FA was higher in mTBI without persistent symptoms relative to OI, d (95% confidence interval) = 0.31 to 0.37 (0.02, 0.68), across time. In younger children, MD of the anterior thalamic radiations was higher in mTBI with persistent symptoms relative to both mTBI without persistent symptoms, 1.43 (0.59, 2.27), and OI, 1.94 (1.07, 2.81). MD of the arcuate fasciculus, -0.58 (-1.04, -0.11), and superior longitudinal fasciculus, -0.49 (-0.90, -0.09) was lower in mTBI without persistent symptoms relative to OI at 6 months post-injury. White matter microstructural changes suggesting neuroinflammation and axonal swelling occurred chronically and continued 6 months post injury in children with mTBI, especially in younger children with persistent symptoms, relative to OI. White matter microstructure appears more organized in children without persistent symptoms, consistent with their better clinical outcomes.

Indexed as

Brain ConcussionWhite MatterBrainChildDiffusion Tensor ImagingHumansLongitudinal StudiesProspective Studiesconcussiondiffusion tensor imagingmild orthopedic injurypediatric mild traumatic brain injurypediatric traumatic injurypost-concussive symptoms

Identifiers

PMID35467058
PMCPMC9294335
OpenAlexW4224438895

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.