Evidence map›Paper›PMID 40177201›Full record

ReviewWorld journal of hepatology2025

Gut microbiota differences, metabolite changes, and disease intervention during metabolic - dysfunction - related fatty liver progression.

Jian-Zhong Shu, Yu-Han Huang, Xiao-Hong He, Feng-Ying Liu, Qian-Qian Liang, Xue-Tong Yong, Yong-Fang Xie

Abstract readReview
In one paragraph

Review in World journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
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  5. Review
  6. Review
  7. 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

7 authors.

Jian-Zhong ShuDepartment of Encephalopathy, Chongqing Hospital of Traditional Chinese Medicine, Chongqing 400015, China.
Yu-Han HuangSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
Xiao-Hong HeSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
Feng-Ying LiuSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
Qian-Qian LiangSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
Xue-Tong YongSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.
Yong-Fang XieSchool of Life Health Information Science and Engineering, Chongqing University of Posts and Telecommunications, Chongqing 400065, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the current era, metabolic dysfunction-associated steatotic liver disease (MASLD) has gradually developed into a major type of chronic liver disease that is widespread globally. Numerous studies have shown that the gut microbiota plays a crucial and indispensable role in the progression of MASLD. Currently, the gut microbiota has become one of the important entry points for the research of this disease. Therefore, the aim of this review is to elaborate on the further associations between the gut microbiota and MASLD, including the changes and differences in the microbiota between the healthy liver and the diseased liver. Meanwhile, considering that metabolic dysfunction-associated fatty liver and metabolic dysfunction-associated steatohepatitis are abnormal pathological states in the development of the disease and that the liver exhibits different degrees of fibrosis (such as mild fibrosis and severe fibrosis) during the disease progression, we also conduct a comparison of the microbiota in these states and use them as markers of disease progression. It reveals the changes in the production and action mechanisms of short-chain fatty acids and bile acids brought about by changes in the gut microbiota, and the impact of lipopolysaccharide from Gram-negative bacteria on the disease. In addition, the regulation of the gut microbiota in disease and the production and inhibition of related disease factors by the use of probiotics (including new-generation probiotics) will be explored, which will help to monitor the disease progression of patients with different gut microbiota compositions in the future and carry out personalized targeted therapies for the gut microbiota. This will achieve important progress in preventing and combating this disease.

Indexed as

Bile acidsGut microbiotaLipopolysaccharidesMetabolic dysfunction-associated steatotic liver diseaseProbioticsShort-chain fatty acids

Identifiers

PMID40177201
PMCPMC11959672

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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.