Evidence map›Paper›PMID 39343617›Full record

ReviewJournal of gastroenterology and hepatology2025

Interplay among IL1R1, gut microbiota, and bile acids in metabolic dysfunction-associated steatotic liver disease: a comprehensive review.

Jie-Lun Ku, Jia-Rou Hsu, Yung-Tsung Li, Li-Ling Wu

Abstract readReview
In one paragraph

Review in Journal of gastroenterology and hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. MASLD beyond the liver: decoding the gut-genetic-metabolic nexus.Frontiers in gastroenterology (Lausanne, Switzerland) · 2026
    Review
  2. Article
  3. Article
  4. Review
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.

Jie-Lun KuSchool of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0009-0002-6168-5093
Jia-Rou HsuDepartment and Institute of Physiology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0009-0002-5141-6180
Yung-Tsung LiGraduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, 100, Taiwan.ORCID https://orcid.org/0000-0003-0135-5260
Li-Ling WuDepartment and Institute of Physiology, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-2293-6999

Funding

Ministry of Science and Technology 108-2320-B-010-045-MY3Ministry of Science and Technology 110-2320-B-002-080-MY3Ministry of Science and Technology MOST 111-2314-B-A49-072National Science and Technology Council NSTC 112-2314-B-A49-028-MY3National Science and Technology Council NSTC 112-2740-B-A49-002National Science and Technology Council NSTC 113-2321-B-A49-014-National Science and Technology Council NSTC 113-2740-B-A49-003Yen Tjing Ling Medical Foundation CI-110-22Yen Tjing Ling Medical Foundation CI-111-24
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent metabolic disorder characterized by hepatic steatosis associated with metabolic abnormalities. Recent research has shed light on the intricate interplay among interleukin-1 receptor 1 (IL1R1), gut microbiota, and bile acids in the pathogenesis of MASLD. This review aims to provide a comprehensive overview of the current understanding of the role of IL1R1, gut microbiota, and bile acids in MASLD, exploring their interrelationships and potential mechanisms. We summarize the evidence supporting the involvement of IL1R1 in inflammation, discuss the influence of gut microbiota on bile acid metabolism and its influence on liver health, and elucidate the bidirectional interactions among IL1R1 signaling, gut microbiota composition, and bile acid homeostasis in MASLD. Furthermore, we highlight emerging therapeutic strategies targeting these interrelated pathways for the management of MASLD.

Indexed as

Bile Acids and SaltsFatty LiverGastrointestinal MicrobiomeReceptors, Interleukin-1 Type IAnimalsHomeostasisHumansSignal TransductionBile Acids and SaltsReceptors, Interleukin-1 Type I

Identifiers

PMID39343617
PMCPMC11771549

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.