Evidence map›Paper›PMID 32404926›Full record

ArticleScientific reports2020

Antecedent presentation of neurological phenotypes in the Collaborative Cross reveals four classes with complex sex-dependencies.

Raena Eldridge, Daniel Osorio, Katia Amstalden, Caitlin Edwards, Colin R Young, James J Cai, Kranti Konganti, Andrew Hillhouse, David W Threadgill, C Jane Welsh and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  14. Genetic and immunological contributors to virus-induced paralysis.Brain, behavior, & immunity - health · 2021
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  16. 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.

Raena Eldridge *Texas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.ORCID http://orcid.org/0000-0002-4450-9971
Daniel Osorio *Texas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.ORCID http://orcid.org/0000-0003-4424-8422
Katia AmstaldenTexas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.
Caitlin EdwardsUniversity of North Carolina, Department of Epidemiology, Chapel Hill, USA.ORCID http://orcid.org/0000-0003-4228-2192
Colin R YoungTexas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.
James J CaiTexas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.
Kranti KongantiTexas A&M Institute for Genome Sciences and Society, College Station, USA.
Andrew HillhouseTexas A&M Institute for Genome Sciences and Society, College Station, USA.
David W ThreadgillTexas A&M University, Department of Molecular and Cellular Medicine, College Station, USA.ORCID http://orcid.org/0000-0003-3538-1635
C Jane WelshTexas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA.
Candice Brinkmeyer-LangfordTexas A&M University, Department of Veterinary Integrative Biosciences, College Station, USA. brinkmeyer@tamu.edu.

Funding

Host genetic determinants of diversity in viral-induced neuropathologyR01NS103934 · NINDS · TEXAS A&M UNIVERSITY · PI BRINKMEYER-LANGFORD, CANDICE L. · 2018 to 2022
$1.6M
NINDS NIH HHS R01 NS103934
6 · The paper itself

Abstract

Antecedent viral infection may contribute to increased susceptibility to several neurological diseases, such as multiple sclerosis and Parkinson's disease. Variation in clinical presentations of these diseases is often associated with gender, genetic background, or a combination of these and other factors. The complicated etiologies of these virally influenced diseases are difficult to study in conventional laboratory mouse models, which display a very limited number of phenotypes. We have used the genetically and phenotypically diverse Collaborative Cross mouse panel to examine complex neurological phenotypes after viral infection. Female and male mice from 18 CC strains were evaluated using a multifaceted phenotyping pipeline to define their unique disease profiles following infection with Theiler's Murine Encephalomyelitis Virus, a neurotropic virus. We identified 4 distinct disease progression profiles based on limb-specific paresis and paralysis, tremors and seizures, and other clinical signs, along with separate gait profiles. We found that mice of the same strain had more similar profiles compared to those of different strains, and also identified strains and phenotypic parameters in which sex played a significant role in profile differences. These results demonstrate the value of using CC mice for studying complex disease subtypes influenced by sex and genetic background. Our findings will be useful for developing novel mouse models of virally induced neurological diseases with heterogenous presentation, an important step for designing personalized, precise treatments.

Indexed as

Crosses, GeneticGenetic Association StudiesPhenotypeAnimalsCluster AnalysisEncephalitisFemaleGaitH-2 AntigensMaleMicePoliomyelitisSeizuresSex FactorsSpecies SpecificityTheilovirusH-2 Antigens

Identifiers

PMID32404926
PMCPMC7220920

What OpenQuestion holds

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LicenceCC BY
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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.