Evidence map›Paper›PMID 40961093›Full record

ArticlePloS one2025

Pre-infection cerebral cortex structure predicts murine sepsis outcome.

Robert M Gallant, Shahinur Alam, Krishnan Venkataraman, Benjamin S McKenna, Khaled Khairy, Janelle S Ayres

Abstract read
In one paragraph

Article in PloS one, 2025. 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

6 authors.

Robert M GallantMolecular and Systems Physiology Lab, Salk Institute for Biological Studies, La Jolla, California, United States of America.ORCID 0000-0003-1741-5336
Shahinur AlamCenter for Bioimage Informatics, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Krishnan VenkataramanCenter for Bioimage Informatics, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Benjamin S McKennaPacific Treatment and Research Center, Department of Psychiatry, University of California, San Diego, San Diego, California, United States of America.
Khaled KhairyCenter for Bioimage Informatics, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Janelle S AyresMolecular and Systems Physiology Lab, Salk Institute for Biological Studies, La Jolla, California, United States of America.ORCID 0000-0002-0809-2494

Funding

GENETIC MECHANISMS AND REGULATIONT32GM007240 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMPTON, RANDOLPH Y. · 1985 to 2019
$23.8M
Pathways in Biological Sciences Training ProgramT32GM133351 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Matthew Daugherty, Randolph Y. Hampton · 2020 to 2026
$9.9M
Host-microbe interactions: Harnessing co-evolution to treat diseaseDP1AI144249 · NIAID · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI AYRES, JANELLE S · 2018 to 2022
$6.7M
The role of serotonin in cooperative defenses during polymicrobial sepsisF31AI169988 · NIAID · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GALLANT, ROBERT MARC · 2023 to 2024
$60k
NIAID NIH HHS DP1 AI144249NIAID NIH HHS F31 AI169988NIGMS NIH HHS T32 GM007240NIGMS NIH HHS T32 GM133351
6 · The paper itself

Abstract

Sepsis is a life-threatening condition caused by an inappropriate host response to an infection that can lead to multi-organ failure and death. Predictive markers that can inform the trajectory and outcome for a septic patient are necessary to inform treatment and increase the likelihood for patient survival. Here, by leveraging the concept of Lethal Dose 50 (LD50), which is the dose of a pathogen that will kill 50% of a genetically identical host population, we tested the hypothesis that variations in brain structure can be readily used to predict trajectory and outcome in a murine model of sepsis. We found that one week prior to infection, mice that were fated to survive exhibited greater cortical volume, solidity, and thickness compared to those who would succumb to the LD50 challenge, and these metrics were sufficient to train multiple predictive models with 75% to 94% accuracy. Our work reveals a readily measurable non-genetic marker for predicting sepsis prognosis in mice and demonstrates the potential for using pre-infection high-resolution structural brain scans to predict infection outcomes in humans.

Indexed as

Cerebral CortexSepsisAnimalsDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLPrognosis

Identifiers

PMID40961093
PMCPMC12443313

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.