Evidence map›Paper›PMID 40065353›Full record

ArticleJournal of translational medicine2025

Identification of enterotype for patients with Alzheimer's disease.

Guang-Sheng Liu, Yang Song, Jin-Sheng Yan, Yi-Jie Chai, Yun-Fei Zhao, Huan Ma

Abstract read
In one paragraph

Article in Journal of translational medicine, 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

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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

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

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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

6 authors.

Guang-Sheng Liu *Department of Neurosurgery, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Yang Song *Department of Neurosurgery, Linfen People's Hospital, Linfen, China.
Jin-Sheng Yan *Department of Neurosurgery, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Yi-Jie ChaiThe Second Clinical School of Medicine, Shanxi Medical University, Taiyuan, China.
Yun-Fei ZhaoDepartment of Neurology, The Second Hospital of Shanxi Medical University, Taiyuan, China. yunfeizhao1218@163.com.
Huan MaDepartment of Anesthesiology, The Second Hospital of Shanxi Medical University, Taiyuan, China. mahuan202412@163.com.ORCID 0009-0002-8453-4992

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a progressive and chronic neurodegenerative disorder of the central nervous system, characterized by behavioral and dysexecutive deficits. Its pathogenesis is closely associated with the intestinal flora. This study aimed to explore the enterotypes in AD by identifying key bacteria through machine learning and species co-occurrence network analysis.

methodsThe collection of fecal samples from AD patients was followed by 16 S rRNA analysis using QIIME2. Enterotype clustering was conducted at the genus level, and deep neural network (DNN) classification models were developed for AD and healthy controls within each enterotype.

resultsAnalysis of three 16 S rRNA gut microbiome datasets identified three distinct enterotypes: Escherichia_Shigella (ET-E), Faecalibacterium (ET-F), and Bacteroides (ET-B). The ET-E is mainly characterized by the absence of Akkermansia in AD group. The Akkermansia was significantly positively correlated with Eubacterium_coprostanoligenes_group and negatively correlated with biosynthesis and amino acid metabolism. The ET-F highly expressed Agathobacter, un_f__Lachnospiraceae, Lachnoclostridium, and low expressed Dorea in AD group. Among them, Agathobacter was significantly positively correlated with un_f__Lachnospiraceae, and un_f__Lachnospiraceae was significantly positively correlated with Lachnoclostridium. The Dorea was significantly negatively correlated with Lachnoclostridium. The AD from ET-B group had high expression of two beneficial bacteria, Butyricicoccus and Parabacteroides. The findings suggest that the ET-E enterotype may predispose individuals to AD, with Akkermansia identified as a potential risk factor. Conversely, the ET-B enterotype appears to be associated with milder symptoms, with Butyricicoccus and Parabacteroides potentially serving as protective factors. Therefore, a comprehensive understanding of the species characteristics and interactions within different enterotypes is essential for modulating the gut-brain axis and mitigating AD symptoms.

Indexed as

Alzheimer DiseaseGastrointestinal MicrobiomeAgedBacteriaCase-Control StudiesCluster AnalysisFecesFemaleHumansMaleRNA, Ribosomal, 16SRNA, Ribosomal, 16SAkkermansiaAlzheimer’s diseaseButyricicoccusCo-occurrence networkEnterotypesGut microbiomeMachine learningParabacteroides

Identifiers

PMID40065353
PMCPMC11892252

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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.