Evidence map›Paper›PMID 37493939›Full record

ArticleTranslational stroke research2024

Neurobehavioral Impairments Predict Specific Cerebral Damage in Rat Model of Subarachnoid Hemorrhage.

Daniel G Lynch, Kevin A Shah, Keren Powell, Steven Wadolowski, Willians Tambo, Joshua J Strohl, Prashin Unadkat, David Eidelberg, Patricio T Huerta, Chunyan Li

Abstract read
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In one paragraph

Article in Translational stroke research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Daniel G LynchTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Kevin A ShahTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Keren PowellTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Steven WadolowskiTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Willians TamboTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Joshua J StrohlZucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.
Prashin UnadkatDepartment of Neurosurgery, North Shore University Hospital, Manhasset, NY, USA.
David EidelbergZucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.
Patricio T HuertaZucker School of Medicine at Hofstra/Northwell, Hempstead, NY, USA.
Chunyan LiTranslational Brain Research Laboratory, The Feinstein Institutes for Medical Research, Manhasset, NY, USA. cli11@northwell.edu.
Feinstein Institute for Medical Research · USNorthwell Health · US

Funding

Trigeminal nerve stimulation to modulate cortical spreading depolarizations after brain injuryR21NS114763 · NINDS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI LI, CHUNYAN · 2020 to 2021
$461k
NINDS NIH HHS R21 NS114763
6 · The paper itself

Abstract

Subarachnoid hemorrhage (SAH) is a severe form of stroke that can cause unpredictable and diffuse cerebral damage, which is difficult to detect until it becomes irreversible. Therefore, there is a need for a reliable method to identify dysfunctional regions and initiate treatment before permanent damage occurs. Neurobehavioral assessments have been suggested as a possible tool to detect and approximately localize dysfunctional cerebral regions. In this study, we hypothesized that a neurobehavioral assessment battery could be a sensitive and specific method for detecting damage in discrete cerebral regions following SAH. To test this hypothesis, a behavioral battery was employed at multiple time points after SAH induced via an endovascular perforation, and brain damage was confirmed via postmortem histopathological analysis. Our results demonstrate that impairment of sensorimotor function accurately predict damage in the cerebral cortex (AUC 0.905; sensitivity 81.8%; specificity 90.9%) and striatum (AUC 0.913; sensitivity 90.1%; specificity 100%), while impaired novel object recognition is a more accurate indicator of damage to the hippocampus (AUC 0.902; sensitivity 74.1%; specificity 83.3%) than impaired reference memory (AUC 0.746; sensitivity 72.2%; specificity 58.0%). Tests for anxiety-like and depression-like behaviors predict damage to the amygdala (AUC 0.900; sensitivity 77.0%; specificity 81.7%) and thalamus (AUC 0.963; sensitivity 86.3%; specificity 87.8%), respectively. This study suggests that recurring behavioral testing can accurately predict damage in specific brain regions, which could be developed into a clinical battery for early detection of SAH damage in humans, potentially improving early treatment and outcomes.

Indexed as

Disease Models, AnimalRats, Sprague-DawleySubarachnoid HemorrhageAnimalsBehavior, AnimalMaleRatsDelayed cerebral ischemiaEarly brain injuryNeurobehavioral dysfunctionRegional brain damageSubarachnoid hemorrhage

Identifiers

PMID37493939
OpenAlexW4385264593

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.