Evidence map›Paper›PMID 42416276›Full record

ReviewFrontiers in cellular and infection microbiology2026

The bile acid-gut microbiota-vitamin D axis: new insights into biliary atresia.

Chu Huang, Zongxian Li, Wei Shen, Meilin Luo, Faquan Lin

Abstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 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.

Chu Huang *Department of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University. Key Laboratory of Clinical Laboratory Medicine of Guangxi Medical University, Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Zongxian Li *Department of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University. Key Laboratory of Clinical Laboratory Medicine of Guangxi Medical University, Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Wei ShenDepartment of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University. Key Laboratory of Clinical Laboratory Medicine of Guangxi Medical University, Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Meilin LuoDepartment of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University. Key Laboratory of Clinical Laboratory Medicine of Guangxi Medical University, Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Faquan LinDepartment of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University. Key Laboratory of Clinical Laboratory Medicine of Guangxi Medical University, Education Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biliary atresia (BA) is a progressive fibroinflammatory disease affecting both intrahepatic and extrahepatic bile ducts. It leads to cholestasis, hepatic fibrosis, and eventually biliary cirrhosis. Although BA is the most common cause of neonatal cholestasis, its exact pathogenesis remains incompletely understood. Emerging evidence suggests that disturbances in bile acid metabolism, gut microbiota dysbiosis, and vitamin D deficiency may play critical roles in the initiation and progression of BA. This review systematically summarizes the dynamic evolution characteristics of bile acid profiles, gut microbiota composition, and vitamin D levels in children with BA across different disease stages. It further explores the potential positive feedback loop effects of the bile acid-gut microbiota-vitamin D axis in the pathogenesis and progression of the disease. Additionally, this review discusses potential diagnostic value and therapeutic strategies based on this axis. Interventions targeting bile acid metabolism, modulating the gut microbiota, and supplementing vitamin D have shown promise in altering the disease course. Despite these advances, further research is needed to elucidate the precise molecular mechanisms underlying this axis in BA. Such knowledge will pave the way for more effective preventive and therapeutic strategies for this complex disease.

Indexed as

Bile Acids and SaltsBiliary AtresiaGastrointestinal MicrobiomeVitamin DAnimalsDysbiosisHumansVitamin D DeficiencyBile Acids and SaltsVitamin Dbile acidbiliary atresiagut microbiotapositive feedback loopvitamin D

Identifiers

PMID42416276
PMCPMC13337835

What Socratic holds

Textmetadata
LicenceCC BY
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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.