Evidence map›Paper›PMID 41035890›Full record

ArticleFrontiers in microbiology2025

The analysis of the gut microbiome during liver disease progression led to the identification of biomarkers for related mild cognitive impairment.

Lola Giner-Pérez, Juan-José Gallego, Carla Gimènez-Garzó, Daniela Batallas, Víctor H Jarquín-Díaz, Franc Casanova-Ferrer, Alessandra Fiorillo, Amparo Urios, Jennifer N Martínez-Medina, Adrià López-Gramaje and 8 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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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

18 authors.

Lola Giner-Pérez *Laboratory of Lactic Acid Bacteria and Probiotics, Instituto de Agroquímica y Tecnología de Alimentos (IATA-CSIC), Valencia, Spain.
Juan-José Gallego *Laboratory of Lactic Acid Bacteria and Probiotics, Instituto de Agroquímica y Tecnología de Alimentos (IATA-CSIC), Valencia, Spain.
Carla Gimènez-GarzóLaboratory of Neurobiology, Centro de Investigación Príncipe Felipe, Valencia, Spain.
Daniela BatallasLaboratory of Social Cognitive Neuroscience, Department of Psychobiology and IDOCAL, Universidad de Valencia, Valencia, Spain.
Víctor H Jarquín-DíazExperimental and Clinical Research Center, A Cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Franc Casanova-FerrerInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Alessandra FiorilloInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Amparo UriosInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Jennifer N Martínez-MedinaExperimental and Clinical Research Center, A Cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Adrià López-GramajeInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Yaiza M ArenasInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.
Desamparados Escudero-GarcíaServicio de Medicina Digestiva, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Salvador BenllochServicio de Medicina Digestiva, Hospital Arnau de Vilanova, Valencia, Spain.
Alicia SalvadorLaboratory of Social Cognitive Neuroscience, Department of Psychobiology and IDOCAL, Universidad de Valencia, Valencia, Spain.
Vicente FelipoLaboratory of Neurobiology, Centro de Investigación Príncipe Felipe, Valencia, Spain.
Sofia K Forslund-StartcevaExperimental and Clinical Research Center, A Cooperation between the Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Gaspar Pérez MartínezLaboratory of Lactic Acid Bacteria and Probiotics, Instituto de Agroquímica y Tecnología de Alimentos (IATA-CSIC), Valencia, Spain.
Carmina MontoliuInstituto de Investigación Sanitaria INCLIVA, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Although it is well established that liver disease is associated with alterations in the gut microbiome (GM), the mechanisms linking these microbial changes to the progression of liver disease-and more critically, to its related cognitive impairment-remain poorly understood. Therefore, to define biomarkers for the early and advanced phases of these conditions, it is necessary to gain insight into changes in the GM throughout the evolution of the disease, particularly regarding the early onset of cognitive decline. Methods: The GM taxonomy and function profiles were defined, data were collected for dietary intake, fecal short-chain fatty acids (SCFA), cognitive status, quality of life and biochemical and immunological blood parameters of patients belonging to different stages of liver disease (MASLD and cirrhosis) and cognitive function. Results: This study showed: 1) the fibrosis stage severity (F1 to F4) in liver disease was associated with reduced GM diversity independently of cognitive status and with a decline in beneficial autochthonous bacteria; 2) Conclusion: In this context, maintaining a balanced production of fecal SCFA is more important than individual concentrations. The downregulation of specific microbial metabolic pathways, along with the presence of certain bacterial species, holds promise as early-stage biomarkers and highlights the potential of microbiome-targeted strategies for monitoring and managing liver-related cognitive impairment.

Indexed as

biomarkerscirrhosiscognitive impairmentgut microbiomemetabolic dysfunction-associated steatotic liver disease (MASLD)minimal hepatic encephalopathy (MHE)neuroinflammationshort-chain fatty acids (SCFA)

Identifiers

PMID41035890
PMCPMC12481516

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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.