Evidence mapPaperPMID 41019148Full record

ArticleJournal of nutrition and metabolism2025

Association of Gut Microbiota-Derived Short-Chain Fatty Acids With Persistent Elevated Serum Transaminase Levels in Normal Weight and Obesity: A Pilot Study.

David Alberto Díaz de Sandy-Galán, Hugo Villamil-Ramírez, Maricela Rodríguez-Cruz, Blanca López-Contreras, Paola León-Mimila, Marisol Olivares-Arévalo, Jorge Maldonado-Hernández, Israel Domínguez-Calderon, Jorge Salmerón, Daniel Cerqueda-García and 3 more

Abstract read
In one paragraph

Article in Journal of nutrition and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

13 authors.

David Alberto Díaz de Sandy-GalánUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.
Hugo Villamil-RamírezUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.ORCID https://orcid.org/0009-0007-4425-2241
Maricela Rodríguez-CruzLaboratory of Molecular Nutrition, Medical Nutrition Research Unit, Pediatric Hospital, National Medical Center "21st Century", Mexican Social Security Institute (IMSS), Mexico City 06720, Mexico.ORCID https://orcid.org/0000-0001-8496-4023
Blanca López-ContrerasUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.ORCID https://orcid.org/0000-0003-2089-0170
Paola León-MimilaUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.ORCID https://orcid.org/0000-0001-6334-1492
Marisol Olivares-ArévaloUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.ORCID https://orcid.org/0009-0004-6687-3100
Jorge Maldonado-HernándezLaboratory of Molecular Nutrition, Medical Nutrition Research Unit, Pediatric Hospital, National Medical Center "21st Century", Mexican Social Security Institute (IMSS), Mexico City 06720, Mexico.ORCID https://orcid.org/0000-0002-7592-7025
Israel Domínguez-CalderonLaboratory of Molecular Nutrition, Medical Nutrition Research Unit, Pediatric Hospital, National Medical Center "21st Century", Mexican Social Security Institute (IMSS), Mexico City 06720, Mexico.ORCID https://orcid.org/0000-0002-2384-8552
Jorge SalmerónResearch Center in Policies, Population and Health, School of Medicine, UNAM, Mexico City 04510, Mexico.
Daniel Cerqueda-GarcíaBiorational Pest and Vector Management Network, Biomimic® Scientific and Technological Cluster, Ecology Institute AC, Xalapa 91073, Mexico.ORCID https://orcid.org/0000-0003-1544-5662
Teresa Villarreal-MolinaGenomics of Cardiovascular Disease Laboratory, INMEGEN, Mexico City 14610, Mexico.ORCID https://orcid.org/0000-0003-4450-7690
Rafael Velázquez-CruzGenomics of Bone Metabolism Laboratory, INMEGEN, Mexico City 14610, Mexico.ORCID https://orcid.org/0000-0003-4515-0777
Samuel Canizales-QuinterosUnit of Population Genomics Applied to Health, Department of Biology, School of Chemistry, National Autonomous University of Mexico (UNAM), National Institute of Genomic Medicine (INMEGEN), Mexico City 14610, Mexico.ORCID https://orcid.org/0000-0002-4833-6932

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although obesity is the most common risk factor for hepatic steatosis, this disease may occur in normal-weight individuals. While gut microbial metabolites such as short-chain fatty acids (SCFAs) have been associated with obesity and metabolic disease, the relationship among fecal SCFA concentrations, SCFA-producing bacteria, and hepatic steatosis with and without obesity is not fully understood. This pilot study aimed to compare fecal SCFA concentrations and SCFA-producing gut bacteria in four study groups: 7 individuals with normal-weight and normal alanine aminotransferase levels (Nw-N ALT), 7 individuals with normal-weight and elevated ALT levels (Nw-E ALT), 12 individuals with obesity and normal ALT levels and (Ob-N ALT), and 18 individuals with obesity and elevated ALT levels (Ob-E ALT). Fecal SCFA concentrations were quantified using gas chromatography, and gut microbiota was characterized by sequencing 16S rRNA. Median fecal SCFA concentrations (propionate, butyrate, and valerate) were highest in the Ob-E ALT group and lowest in the Nw-N ALT group (

Indexed as

gut microbiotahepatic steatosisshort-chain fatty acidstransaminases

Identifiers

PMID41019148
PMCPMC12476282

What Socratic holds

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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.