Evidence map›Paper›PMID 26661216›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2016

Robust effects of genetic background on responses to subarachnoid hemorrhage in mice.

Josephine A D'Abbondanza, Jinglu Ai, Elliot Lass, Hoyee Wan, Shakira Brathwaite, Michael K Tso, Charles Lee, Philip A Marsden, R Loch Macdonald

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Different Responses to Identical Trauma Between BALB/C and C57BL/6 Mice.Medical science monitor : international medical journal of experimental and clinical research · 2021
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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 2 institutions in 1 country.

Josephine A D'AbbondanzaDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Jinglu AiDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Elliot LassDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Hoyee WanDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Shakira BrathwaiteDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Michael K TsoDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Charles LeeDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada.
Philip A MarsdenKeenan Research Centre for Biomedical Science and the Li Ka Shing Knowledge Institute of St. Michael's Hospital, Toronto, ON, Canada.
R Loch MacdonaldDivision of Neurosurgery, St. Michael's Hospital, Toronto, ON, Canada macdonaldlo@smh.ca.
St. Michael's Hospital · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Outcome varies among patients with subarachnoid hemorrhage but known prognostic factors explain only a small portion of the variation in outcome. We hypothesized that individual genetic variations influence brain and vascular responses to subarachnoid hemorrhage and investigated this using inbred strains of mice.Subarachnoid hemorrhage was induced in seven inbred and a chromosome 7 substitution strain of mouse. Cerebral blood flow, vasospasm of the middle cerebral artery, and brain injury were assessed. After 48 h of subarachnoid hemorrhage, mice showed significant middle cerebral artery vasospasm that correlated positively with reduction in cerebral blood flow at 45 min. Mice also had increased neuronal injury compared to sham controls; A/J and C57BL/6 J strains represented the most and least severe, respectively. However, brain injury did not correlate with cerebral blood flow reduction at 45 min or with vasospasm at 48 h. Chromosome 7 substitution did not influence the degree of vasospasm or brain injury.Our data suggested that mouse genetic background influences outcome of subarachnoid hemorrhage. Investigations into the genetic factors causing these inter-strain differences may provide insight into the etiology of the brain damage following subarachnoid hemorrhage. These findings also have implications for animal modeling of disease and suggest that genetic differences may also modulate outcome in other cardiovascular diseases.

Indexed as

Genetic BackgroundAnimalsApoptosisCerebrovascular CirculationDisease Models, AnimalMaleMice, Inbred BALB CMice, Inbred C57BLMice, Inbred DBAMiddle Cerebral ArterySpecies SpecificitySubarachnoid HemorrhageVasospasm, IntracranialGenetic variationmouseneuronal cell deathsubarachnoid hemorrhage

Identifiers

PMID26661216
PMCPMC5094306
OpenAlexW2201560052

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.