Evidence map›Paper›PMID 42100141›Full record

ArticleClinical immunology communications2026

Sexual dimorphism in the colonic microbiome and host's transcriptomics profiles of a murine model of multiple sclerosis.

William J Doyle, Sean M Schumacher, Megan R Gates, Natalie Sofaly, Ella Angelo, Hannah Hedelius, David R Johnson, Joshua Wells, Michael Perlmutter, Kacey Caradonna and 1 more

Abstract read
In one paragraph

Article in Clinical immunology communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

William J DoyleBiomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.
Sean M SchumacherBiomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.
Megan R GatesBiomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.ORCID 0009-0004-5041-5711
Natalie SofalyDepartment of Biological Sciences, Boise State University, Boise, ID 83725, USA.
Ella AngeloDepartment of Biological Sciences, Boise State University, Boise, ID 83725, USA.
Hannah HedeliusBiomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.
David R JohnsonComputing Ph.D. Program, Boise State University, Boise, ID 83725, USA.ORCID 0009-0000-2537-7806
Joshua WellsBiology, Brigham Young University-Idaho, Rexburg, ID 83460, USA.
Michael PerlmutterComputing Ph.D. Program, Boise State University, Boise, ID 83725, USA.
Kacey CaradonnaHooke Laboratories LLC, 439 S Union St, Lawrence, MA 01843, USA.
Javier Ochoa-RepárazBiomolecular Sciences Graduate Program, Boise State University, Boise, ID 83725, USA.ORCID 0000-0001-9610-3175

Funding

Optimizing Deep Brain Stimulation for Parkinson's Disease.P20GM148321 · NIGMS · BOISE STATE UNIVERSITY · PI Javier Ochoa-Reparaz · 2023 to 2026
$10.2M
Center of Biomedical Research Excellence in Matrix Biology Phase 3P30GM154497 · NIGMS · BOISE STATE UNIVERSITY · PI Katherine J Johnson · 2024 to 2026
$4.2M
Targeting the GABA-modulator microbiota against the progression of CNS inflammatory demyelinationR15NS107743 · NINDS · EASTERN WASHINGTON UNIVERSITY · PI OCHOA-REPARAZ, JAVIER, ROULLET, JEAN-BAPTISTE O · 2019 to 2019
$419k
NIGMS NIH HHS P20 GM148321NIGMS NIH HHS P30 GM154497NINDS NIH HHS R15 NS107743
6 · The paper itself

Abstract

Background: Multiple Sclerosis is a chronic autoimmune disease that attacks the myelin sheath in the central nervous system, with a higher prevalence among female patients. We and others have documented significant changes in microbial taxa in response to the induction of active experimental autoimmune encephalomyelitis (EAE), an MS model. Objective: To evaluate sex as a biological variable in both the host and colonic microenvironment during active EAE. Methods: We conducted colonic transcriptomics and microbiota analysis of colonic fecal content in male and female EAE C57BL/6 J mice and controls at the time of disease induction, pre-onset, and peak disease. Results: Analysis showed significant sex-specific differences in colonic gene expression during EAE. As disease severity increased, the profiles of colon microbiome and transcriptomics became less distinct. Conclusions: Our results suggest early changes in colonic inflammatory pathways, with notable differences between males and females associated with microbiota alterations triggered by disease induction.

Indexed as

ColonEAEInflammationMicrobiomeMSTranscriptomics

Identifiers

PMID42100141
PMCPMC13148278

What Socratic holds

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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 Socratic graph.