Evidence map›Paper›PMID 34375128›Full record

ArticleJournal of neurotrauma2021

Visual Dysfunction after Repetitive Mild Traumatic Brain Injury in a Mouse Model and Ramifications on Behavioral Metrics.

Nicholas J Morriss, Grace M Conley, Nathaniel Hodgson, Masen Boucher, Sara Ospina-Mora, Michaela Fagiolini, Mark Puder, Leo Mejia, Jianhua Qiu, William Meehan and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of neurotrauma, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  7. Blast injury: Impact to the cornea.Experimental eye research · 2024
    Review
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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

11 authors at 1 institution in 1 country.

Nicholas J MorrissDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Grace M ConleyDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Nathaniel HodgsonDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Masen BoucherDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Sara Ospina-MoraDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Michaela FagioliniDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Mark PuderHarvard Medical School, Boston, Massachusetts, USA.
Leo MejiaDepartment of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Jianhua QiuDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
William MeehanHarvard Medical School, Boston, Massachusetts, USA.
Rebekah MannixDivision of Emergency Medicine, Boston Children's Hospital, Boston, Massachusetts, USA.
Boston Children's Hospital · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Mild traumatic brain injury (mTBI) is a major cause of morbidity and mortality with a poorly understood pathophysiology. Animal models have been increasingly utilized to better understand mTBI and recent research has identified visual deficits in these models that correspond to human literature. While visual impairment is being further characterized within TBI, the implications of impaired vision on behavioral tasks commonly utilized in animal models has not been well described thus far. Visual deficits may well confound behavioral tests that are believed to be isolated to cognitive functioning such as learning and memory. We utilized a mouse model of repetitive mTBI (rmTBI) to further characterize visual deficits using an optomotor task, electroretinogram, and visually evoked potential, and located likely areas of damage to the visual pathway. Mice were tested on multiple behavioral metrics, including a touchscreen conditional learning task to better identify the contribution of visual dysfunction to behavioral alterations. We found that rmTBI caused visual dysfunction resulting from damage distal to the retina that likely involves pathology within the optic nerve. Moreover, loss of vision led to poorer performance of rmTBI animals on classic behavioral tests such as the Morris water maze that would otherwise be attributed solely to learning and memory deficits. The touchscreen conditional learning task was able to differentiate rmTBI induced learning and memory dysfunction from visual impairment and is a valuable tool for elucidating subtle changes resulting from TBI.

Indexed as

Behavior, AnimalAnimalsBrain ConcussionCognitionConditioning, OperantElectroretinographyEvoked Potentials, VisualLearningMaleMaze LearningMemoryMiceMice, Inbred C57BLOptic Nerve InjuriesPsychomotor PerformanceRecurrenceanimal modelbehaviorERGTBIvision

Identifiers

PMID34375128
PMCPMC10495212
OpenAlexW3190231529

What OpenQuestion holds

Textmetadata
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.