Evidence map›Paper›PMID 42515794›Full record

ReviewPharmaceuticals (Basel, Switzerland)2026

Gut Microbiota and Metabolic Dysfunction-Associated Steatotic Liver Disease: From Dysbiosis to Metagenomic Insights and Therapeutic Perspectives.

Otilia Elena Frăsinariu, Violeta Ștreangă, Aniela Luminița Rugină, Dana Elena Mîndru, Teodora Cristina Vintilă, Oana Viola Bădulescu, Iris Bararu-Bojan, Vasile Valeriu Lupu, Ancuța Lupu, Adriana Mihai and 3 more

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 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

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

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

13 authors.

Otilia Elena FrăsinariuGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.ORCID 0000-0002-5836-1517
Violeta ȘtreangăGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.
Aniela Luminița RuginăGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.
Dana Elena MîndruGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.
Teodora Cristina VintilăEndocrinology Department, Saint Spiridon County Hospital, 700111 Iași, Romania.
Oana Viola BădulescuGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.ORCID 0000-0001-7050-8430
Iris Bararu-BojanGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.
Vasile Valeriu LupuGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.ORCID 0000-0003-2640-8795
Ancuța LupuGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.ORCID 0000-0001-8147-3632
Adriana MihaiGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.ORCID 0009-0007-6133-8784
Isabela Ioana LoghinGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.
Daniela Eugenia PopescuDepartment of Obstetrics-Gynecology and Neonatology, "Victor Babeș" University of Medicine and Pharmacy, 300041 Timișoara, Romania.ORCID 0000-0002-4986-8025
Dragoș Florin TeșoiGrigore T. Popa University of Medicine and Pharmacy, 700115 Iași, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as the most common chronic liver disorder in the pediatric population, closely paralleling the global rise in childhood obesity. Increasing evidence highlights the gut-liver axis as a key contributor to MASLD pathogenesis, with gut microbiota dysbiosis influencing hepatic steatosis through multiple interconnected mechanisms, including increased intestinal permeability, endotoxemia, altered bile acid metabolism, and modulation of host energy homeostasis. In children, the characterization of microbiota signatures associated with MASLD remains challenging due to heterogeneity across studies, age-related microbial dynamics, and methodological variability. This review synthesizes current evidence regarding the role of the gut microbiota in pediatric MASLD, focusing on pathogenetic pathways, reported microbial patterns, and microbiota-targeted therapeutic strategies, while incorporating relevant mechanistic evidence from adult studies where pediatric data remain limited. Although several taxa have been repeatedly associated with pediatric MASLD, findings are not yet sufficiently consistent for clinical application. Interventions such as probiotics, prebiotics, and dietary modulation show promising but still preliminary results, with limited high-quality pediatric trials available. A deeper mechanistic understanding and standardized study designs are needed to clarify causality and to support microbiota-based precision approaches in pediatric MASLD management.

Indexed as

dysbiosisgut–liver axisgut microbiotametabolic dysfunctionpediatric MASLD

Identifiers

PMID42515794
PMCPMC13415186

What Socratic 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 Socratic graph.