Evidence map›Paper›PMID 39769181›Full record

ReviewInternational journal of molecular sciences2024

Gut Microbiota and Liver Dysfunction in Sepsis: The Role of Inflammatory Mediators and Therapeutic Approaches.

Aqsa Shahid, Stephen Chambers, Amy Scott-Thomas, Madhav Bhatia

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. 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.

  1. Review
  2. Article
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  6. Article
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  9. Review
  10. Article
  11. Sepsis and the Liver.Diseases (Basel, Switzerland) · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Review
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  17. 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

4 authors.

Aqsa ShahidDepartment of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
Stephen ChambersDepartment of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.
Amy Scott-ThomasDepartment of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.ORCID 0000-0002-3246-2491
Madhav BhatiaDepartment of Pathology and Biomedical Science, University of Otago, Christchurch 8140, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a life-threatening complication caused by an uncontrolled immune response to infection that can lead to multi-organ dysfunction, including liver injury. Recent research has shown the critical role of gut microbiota in sepsis pathogenesis, with the gut-liver axis playing a crucial role in disease progression. Mechanisms such as the disruption of the gut barrier and liver injury pathways mediated by cytokines, chemokines, adhesion molecules, hydrogen sulfide (H

Indexed as

Gastrointestinal MicrobiomeSepsisAnimalsBiomarkersCytokinesHumansInflammation MediatorsLiverLiver DiseasesBiomarkersCytokinesInflammation Mediatorsgut–liver axisgut microbiotaliversepsistherapeutic targets

Identifiers

PMID39769181
PMCPMC11678143

What OpenQuestion 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 OpenQuestion graph.