Evidence map›Paper›PMID 28790425›Full record

ArticleScientific reports2017

Minimal Long-Term Neurobehavioral Impairments after Endovascular Perforation Subarachnoid Hemorrhage in Mice.

Claudia Fanizzi, Andrew D Sauerbeck, Mihika Gangolli, Gregory J Zipfel, David L Brody, Terrance T Kummer

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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  9. Haemoglobin causes neuronal damageBrain communications · 2020
    Article
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

6 authors at 1 institution in 2 countries.

Claudia FanizziDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA.
Andrew D SauerbeckDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA.
Mihika GangolliDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA.
Gregory J ZipfelDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA.
David L BrodyDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA.
Terrance T KummerDepartment of Neurology, Washington University School of Medicine in St. Louis, Missouri, USA. kummert@wustl.edu.ORCID 0000-0001-8938-8280
Washington University in St. Louis · US

Funding

NERVOUS SYSTEM DEVELOPMENT AND INJURYT32NS007205 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 1985 to 2017
$4.2M
ADVANCED DIFFUSION BIOMARKERS OF BRAIN INJURY IN SUBARACHNOID HEMORRHAGEK08NS094760 · NINDS · WASHINGTON UNIVERSITY · PI KUMMER, TERRANCE T · 2015 to 2018
$680k
NINDS NIH HHS K08 NS094760NINDS NIH HHS T32 NS007205
6 · The paper itself

Abstract

Cognitive deficits are among the most severe and pervasive consequences of aneurysmal subarachnoid hemorrhage (SAH). A critical step in developing therapies targeting such outcomes is the characterization of experimentally-tractable pre-clinical models that exhibit multi-domain neurobehavioral deficits similar to those afflicting humans. We therefore searched for neurobehavioral abnormalities following endovascular perforation induction of SAH in mice, a heavily-utilized model. We instituted a functional screen to manage variability in injury severity, then assessed acute functional deficits, as well as activity, anxiety-related behavior, learning and memory, socialization, and depressive-like behavior at sub-acute and chronic time points (up to 1 month post-injury). Animals in which SAH was induced exhibited reduced acute functional capacity and reduced general activity to 1 month post-injury. Tests of anxiety-related behavior including central area time in the elevated plus maze and thigmotaxis in the open field test revealed increased anxiety-like behavior at subacute and chronic time-points, respectively. Effect sizes for subacute and chronic neurobehavioral endpoints in other domains, however, were small. In combination with persistent variability, this led to non-significant effects of injury on all remaining neurobehavioral outcomes. These results suggest that, with the exception of anxiety-related behavior, alternate mouse models are required to effectively analyze cognitive outcomes after SAH.

Indexed as

Disease Models, AnimalAnimalsCognitive DysfunctionMiceSubarachnoid HemorrhageTime Factors

Identifiers

PMID28790425
PMCPMC5548778
OpenAlexW2739940673

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.