Evidence map›Paper›PMID 41024868›Full record

ReviewWorld journal of hepatology2025

From gut to liver: Exploring the relationship between inflammatory bowel disease and metabolic dysfunction-associated steatotic liver disease.

Marina Amorim Lopes, Ellen Cristina Souza Oliveira, Ana Elisa Valencise Quaglio, Andrey Santos, Marcello Imbrizi, Leticia Evelyn Rocha Mendes, Rodrigo Fedatto Beraldo, Julio Pinheiro Baima, Amanda Luísa Spiller, Daniéla Oliveira Magro and 1 more

Abstract readReview
In one paragraph

Review in World journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. 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

11 authors.

Marina Amorim LopesDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil.
Ellen Cristina Souza OliveiraDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil.
Ana Elisa Valencise QuaglioVerum Ingredients, Botucatu Technology Park, Botucatu 18605-525, São Paulo, Brazil.
Andrey SantosDepartment of Internal Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas 13083-887, São Paulo, Brazil.
Marcello ImbriziDivision of Gastroenterology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas 13083-970, São Paulo, Brazil.
Leticia Evelyn Rocha MendesDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil.
Rodrigo Fedatto BeraldoFaculdade de Medicina, Fundação Dracenense de Educação e Cultura (FUNDEC), Dracena 17910-106, São Paulo, Brazil.
Julio Pinheiro BaimaDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil.
Amanda Luísa SpillerDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil.
Daniéla Oliveira MagroDivision of Gastroenterology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas 13083-970, São Paulo, Brazil.
Ligia Yukie SassakiDepartment of Internal Medicine, Medical School, São Paulo State University (UNESP), Botucatu 18618-687, São Paulo, Brazil. ligia.sassaki@unesp.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD), comprising Crohn's disease and ulcerative colitis, is a chronic condition marked by relapsing inflammation of the gastrointestinal tract. Metabolic dysfunction-associated steatotic liver disease (MASLD) emphasizes the interplay between metabolic alterations and modern lifestyle factors in its pathogenesis. Emerging evidence suggests that individuals with IBD are at increased risk for MASLD, driven by shared mechanisms, including gut dysbiosis, chronic systemic inflammation, and compromised intestinal barrier function. However, MASLD frequently remains underdiagnosed in this population. The gut microbiota plays a central role in modulating these interactions, influencing both intestinal permeability and metabolic regulation. Key pathophysiological mechanisms include alterations in short-chain fatty acid production, particularly reduced butyrate synthesis; disruption of bile acid signaling pathways

Indexed as

Crohn’s diseaseGut microbiotaInflammatory bowel diseaseMetabolic dysfunction-associated steatotic liver diseaseUlcerative colitis

Identifiers

PMID41024868
PMCPMC12476730

What OpenQuestion holds

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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.