Evidence map›Paper›PMID 41716420›Full record

ReviewFrontiers in immunology2026

Pathogenesis and intervention strategies for metabolic dysfunction-associated fatty liver disease from the perspective of the gut-microbiota-liver axis.

Jiabao Liao, Ze Zhou, You Lv, Yiting Zhang, Siyi Liu, Haixia Tang, Fei Qv, Si Wang, Lianhao Yang, Yanming Lu and 3 more

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

13 authors.

Jiabao Liao *The First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Ze Zhou *The First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
You Lv *The First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Yiting ZhangThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Siyi LiuThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Haixia TangThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Fei QvMedical Affairs Department, Jiaxing Hospital of Traditional Chinese Medicine, Jiaxing, China.
Si WangThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Lianhao YangThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Yanming LuThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.
Zhixia YangMedical Affairs Department, Jiaxing Hospital of Traditional Chinese Medicine, Jiaxing, China.
Xuehua XieDepartment of Endocrinology, The First Affiliated Hospital of Yunnan University of Chinese Medicine, Kunming, China.
Mengqiu ShaoThe First Clinical Medical College, Yunnan University of Chinese Medicine, Kunming, Yunnan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trillions of microorganisms in the human gut are important regulators of health, and the gut and liver have a symbiotic relationship with them. The study found that there is bidirectional communication of substances and signals between the gut and liver, and the gut microbiota is an important medium for mediating bidirectional communication in the gut-liver axis. During metabolic dysfunction-associated fatty liver disease (MAFLD) development, the gut microbiota and its metabolites change to different degrees and affect MAFLD pathogenesis through the gut-liver axis. However, the bidirectional communication mechanism between the gut and liver in MAFLD remains unexplored, and further investigation in this domain is warranted. In this review, we summarize the role of the gut-liver axis in the pathogenesis of MAFLD and explore potential therapeutic strategies targeting intestinal microecology (such as probiotic intervention and phage therapy) to provide a theoretical basis for the precise prevention and treatment of MAFLD.

Indexed as

Fatty LiverGastrointestinal MicrobiomeLiverMetabolic DiseasesNon-alcoholic Fatty Liver DiseaseAnimalsHumansProbioticsgut microbiotagut-microbiota-liver axismetabolic dysfunction-associated fatty liver diseasemicrobiota metabolitesmicrobiota-targeted therapy

Identifiers

PMID41716420
PMCPMC12913104

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.