Evidence mapPaperPMID 42344926Full record

ReviewFrontiers in immunology2026

Gut microbial bile salt hydrolase as a metabolic gatekeeper in digestive homeostasis and disease.

Haitao Chu, Xin Song, Chang Liu, Tianjiao Ma, Wanlin Cui

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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

5 authors.

Haitao Chu *Department of Hyperbaric Oxygen Medicine, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Xin Song *Department of Pharmacy, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Chang LiuDepartment of Pediatrics, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Tianjiao MaDepartment of Pediatrics, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Wanlin CuiDepartment of Pediatrics, The First Hospital of China Medical University, Shenyang, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota exerts broad control over host physiology through tightly coordinated metabolic networks. Among these, bile salt hydrolase (BSH), a microbial enzyme, serves as a key mediator of microbiota-host crosstalk. As a key upstream gateway reaction in bile acid metabolism, BSH hydrolyzes conjugated bile acids and reshapes the composition and distribution of the intestinal bile acid pool. This remodeling alters bile acid signaling quality and influences the host energy metabolism, immune homeostasis and intestinal barrier integrity. In this review, we summarize the core biological functions and molecular regulatory mechanisms of microbial BSH in maintaining digestive system homeostasis. We further discuss the association between BSH dysregulation and the development of major digestive diseases, including metabolic dysfunction-associated steatotic liver disease (MASLD), inflammatory bowel disease (IBD) and colorectal cancer (CRC). Finally, we outline emerging precision strategies targeting BSH, including strain-specific probiotics, enzyme activity modulators and dietary interventions. These approaches offer a conceptual framework for microbiota-based therapies in digestive diseases.

Indexed as

AmidohydrolasesDigestive System DiseasesGastrointestinal MicrobiomeHomeostasisAnimalsBile Acids and SaltsHumansIntestinal Barrier FunctionAmidohydrolasesBile Acids and Saltscholoylglycine hydrolasebile acid metabolismBSHdigestive diseasesgut–liver axisgut microbiotamicrobiota-based therapy

Identifiers

PMID42344926
PMCPMC13286798

What Socratic holds

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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 Socratic graph.