Evidence map›Paper›PMID 41896654›Full record

ArticleScientific reports2026

Characteristics of gut microbiota and metabolites in patients with metabolic dysfunction-associated steatotic liver disease and colorectal adenoma.

Yuting Li, Wen Fu, Zhao Xiang, Minzhu Zhao, Xuancheng Xie, Weibo Guo, Ying Zhou, Mengyao Zheng, Jinhui Yang

Abstract read
In one paragraph

Article in Scientific reports, 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

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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

9 authors.

Yuting Li *Department of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650000, Yunnan Province, China.
Wen Fu *Department of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650000, Yunnan Province, China.
Zhao XiangDepartment of Gastroenterology, The People's Hospital of Xishuangbanna Dai Nationality Autonomous Prefecture, Xishuangbanna, 666100, Yunnan Province, China.
Minzhu ZhaoDepartment of Internal Medicine II, Public Health Clinical Center of Chengdu, Chengdu, 610000, Sichuan Province, China.
Xuancheng XieDepartment of Radiology, The First People Hospital Of Yunnan Province, Kunming, 650000, Yunnan Province, China.
Weibo GuoDepartment of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650000, Yunnan Province, China.
Ying ZhouDepartment of Gastroenterology, The Third Xiangya Hospital of Central South University, Changsha, 410000, Hunan Province, China.
Mengyao ZhengDepartment of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650000, Yunnan Province, China.
Jinhui YangDepartment of Gastroenterology, The Second Affiliated Hospital of Kunming Medical University, Kunming, 650000, Yunnan Province, China. yangjinhui@kmmu.edu.cn.

Funding

Innovation Fund for Postgraduate Education of Kunming Medical University 2024B010National Natural Science Foundation of China 82160106Science and Technology Plan Project of Yunnan Provincial Department of Science and Technology 202501AY070001-088Scientific Research Fund Project of Yunnan Provincial Department of Education 2021J0252Scientific Research Fund Project of Yunnan Provincial Department of Education 2025J0270
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) has become one of the most prevalent chronic liver conditions worldwide, with its incidence steadily rising. However, the underlying mechanisms linking MASLD to colorectal adenoma remain unclear, and the role of gut microbiota and metabolites in this association requires further investigation. This study aims to characterise the gut microbiota and metabolites in patients with MASLD and colorectal adenoma. A cohort of 58 MASLD patients was enrolled and stratified into two groups based on colorectal adenoma status: the MASLD with colorectal adenoma group (M-CA group, n = 30) and the MASLD without colorectal adenoma group (M-NCA group, n = 28). The gut microbial ecosystem in the M-CA group showed significant dysregulation, evidenced by a decreased Gut Microbiome Health Index (GMHI) and significantly increased Microbiome Dysbiosis Index (MDI). Linear Discriminant Analysis Effect Size (LEfSe) identified 75 differentially abundant microbial taxa between groups, with Bacteroides vulgatus, Bacteroides ovatus, uncultured bacterium of norank genus of Muribaculaceae family, Muribaculaceae, and norank of Muribaculaceae family being significantly enriched in the M-CA group, representing potential microbial biomarkers for this cohort. Partial Least Squares Discriminant Analysis (PLS-DA) screened 116 differential metabolites. When combined with Random Forest (RF), Support Vector Machine (SVM) and Least Absolute Shrinkage and Selection Operator (LASSO) machine learning algorithms, 16 significantly identified biomarkers were discovered. The joint analysis of both omics revealed that variations in differential metabolite levels were associated with changes in specific microbiota abundances. Kyoto encyclopedia of genes and genomes (KEGG) functional prediction analysis indicated that the coordinated alterations in metabolites and microbiota may collectively influence multiple metabolic pathways, including lipid metabolism, xenobiotics biodegradation and metabolism, amino acid metabolism, carbohydrate metabolism, biosynthesis of other secondary metabolites and nucleotide metabolism. This study revealed that patients with MASLD and colorectal adenoma exhibited significant alterations in the gut microbiota composition and metabolic profile, indicating potential impacts on associated metabolic pathways. These findings provided novel insights and a foundation for future research into potential intervention strategies for this clinical complication.

Indexed as

AdenomaColorectal NeoplasmsGastrointestinal MicrobiomeAgedDysbiosisFemaleHumansMaleMetabolomeMiddle AgedColorectal adenomaGut microbiotaMetabolic dysfunction-associated steatotic liver diseaseMetabolite

Identifiers

PMID41896654
PMCPMC13039989

What Socratic holds

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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 Socratic graph.