Evidence map›Paper›PMID 35422470›Full record

ArticleMolecular psychiatry2022

Mouse models of immune dysfunction: their neuroanatomical differences reflect their anxiety-behavioural phenotype.

Darren J Fernandes, Shoshana Spring, Christina Corre, Andrew Tu, Lily R Qiu, Christopher Hammill, Dulcie A Vousden, T Leigh Spencer Noakes, Brian J Nieman, Dawn M E Bowdish and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Sex chromosomes and hormones independently influence healthy brain development but act similarly after cranial radiation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. CD4Neurobiology of stress · 2024
    Article
  6. 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

13 authors at 5 institutions in 2 countries.

Darren J Fernandes *Mouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-0625-7515
Shoshana Spring *Mouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.
Christina CorreDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Andrew TuDivision of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Lily R QiuDepartment of Preclinical Imaging, Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, UK.
Christopher HammillMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.
Dulcie A VousdenMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.
T Leigh Spencer NoakesMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.
Brian J NiemanMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada.
Dawn M E BowdishDepartment of Medicine, McMaster University, Hamilton, ON, Canada.
Jane A FosterDepartment of Psychiatry and Behavioral Neurosciences, McMaster University, Hamilton, ON, Canada.ORCID http://orcid.org/0000-0002-8579-4705
Mark R Palmert *Division of Endocrinology, The Hospital for Sick Children, Toronto, ON, Canada.
Jason P Lerch *Mouse Imaging Centre, The Hospital for Sick Children, Toronto, ON, Canada. jason.lerch@ndcn.ox.ac.uk.
University of Toronto · CAHospital for Sick Children · CAMcMaster University · CAOntario Institute for Cancer Research · CAUniversity of Oxford · GB

Funding

CIHR
6 · The paper itself

Abstract

Extensive evidence supports the role of the immune system in modulating brain function and behaviour. However, past studies have revealed striking heterogeneity in behavioural phenotypes produced from immune system dysfunction. Using magnetic resonance imaging, we studied the neuroanatomical differences among 11 distinct genetically modified mouse lines (n = 371), each deficient in a different element of the immune system. We found a significant and heterogeneous effect of immune dysfunction on the brains of both male and female mice. However, by imaging the whole brain and using Bayesian hierarchical modelling, we were able to identify patterns within the heterogeneous phenotype. Certain structures-such as the corpus callosum, midbrain, and thalamus-were more likely to be affected by immune dysfunction. A notable brain-behaviour relationship was identified with neuroanatomy endophenotypes across mouse models clustering according to anxiety-like behaviour phenotypes reported in literature, such as altered volume in brains regions associated with promoting fear response (e.g., the lateral septum and cerebellum). Interestingly, genes with preferential spatial expression in the most commonly affected regions are also associated with multiple sclerosis and other immune-mediated diseases. In total, our data suggest that the immune system modulates anxiety behaviour through well-established brain networks.

Indexed as

BrainNeuroanatomyAnimalsAnxietyBayes TheoremDisease Models, AnimalFemaleMagnetic Resonance ImagingMaleMicePhenotype

Identifiers

PMID35422470
PMCPMC9205773
OpenAlexW4226126491

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.