Evidence map›Paper›PMID 40481510›Full record

ArticleBMC medicine2025

Circulating short-chain fatty acids and Mediterranean food patterns. A potential role for the prediction of type 2 diabetes risk: The Di@bet.es Study.

Gemma Llauradó, Lídia Cedó, Elisenda Climent, Joan Badia, Gemma Rojo-Martínez, Juana Flores-Le Roux, Oscar Yanes, Maria Vinaixa, Minerva Granado-Casas, Didac Mauricio and 2 more

Abstract read
In one paragraph

Article in BMC medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 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

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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
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

12 authors.

Gemma Llauradó *Department of Endocrinology and Nutrition, Hospital del Mar, Hospital del Mar Medical Research Institute (IMIM), C/ Pg. Marítim 23-25, 08003, Barcelona, Spain. gllauradoc@gmail.com.
Lídia Cedó *Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Elisenda ClimentDepartment of Endocrinology and Nutrition, Hospital del Mar, Hospital del Mar Medical Research Institute (IMIM), C/ Pg. Marítim 23-25, 08003, Barcelona, Spain.
Joan BadiaStatistics and Bioinformatics Platform, Institute of Health Reserach Pere Virgili (IISPV), Reus, Spain.
Gemma Rojo-MartínezCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Juana Flores-Le RouxDepartment of Endocrinology and Nutrition, Hospital del Mar, Hospital del Mar Medical Research Institute (IMIM), C/ Pg. Marítim 23-25, 08003, Barcelona, Spain.
Oscar YanesCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Maria VinaixaCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Minerva Granado-CasasCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Didac MauricioCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Sonia Fernández-VeledoCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Joan VendrellCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Instituto de Salud Carlos III (ISCIII), Madrid, Spain. jvortega@iispv.cat.

Funding

Agència de Gestió d'Ajuts Universitaris i de Recerca 2021 SGR 0089Agència de Gestió d'Ajuts Universitaris i de Recerca 2021 SGR 01409Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas CB07708/0012Instituto de Salud Carlos III PI18/0328Instituto de Salud Carlos III PI20/00312Instituto de Salud Carlos III PI20/00338'la Caixa' Foundation ID 100010434Ministerio de Ciencia e Innovación PID2020-119030RJ-I00Ministerio de Ciencia e Innovación RTI2018-093919-B-100Sociedad Española de Diabetes XII Ayudas SED a Proyectos de Investigación Clínica en Diabetes dirigidos por jóvenes investigadores
6 · The paper itself

Abstract

backgroundIdentifying nutritional patterns associated with developing type 2 diabetes (T2D) can facilitate more effective and personalized dietary interventions. Short-chain fatty acids (SCFAs), key metabolites derived from gut microbiota, are produced through the anaerobic fermentation of dietary fibers. This study aimed to evaluate whether circulating concentrations of SCFAs are associated with specific food consumption patterns and to assess their association with T2D development in at-risk subjects within a prospective cohort (The Di@bet.es Study).

methodsThe Di@bet.es study is a prospective, population-based study utilizing random cluster sampling from the Spanish population aged over 18 years (n = 5,072). Among these participants, 4,347 were free of T2D at baseline. Follow-up losses were approximately 45%, resulting in a final re-screened sample of 2,408 subjects. A qualitative food frequency questionnaire evaluated Mediterranean diet (MedDiet) adherence and high-fiber food consumption. The risk of developing T2D was assessed using the FINDRISK. Metabolomics-driven analyses of SCFAs were conducted using gas chromatography-mass spectrometry.

resultsSubjects who developed T2D after a median follow-up of seven years had higher baseline circulating concentrations of butyrate and isobutyrate. Circulating concentrations of SCFAs were associated with high-fiber food consumption at baseline. In multivariate analysis, baseline circulating concentrations of butyrate and isobutyrate were independently associated with incident T2D after adjusting for traditional clinical factors. The C-statistics for predicting T2D were 0.847 (95%CI:0.816-0.877) for butyrate and 0.843 (95%CI:0.812-0.875) for isobutyrate in adjusted models, similar to the reference model based on traditional clinical factors (0.840 [95%CI: 0.807-0.873]). Both models improved risk prediction compared to FINDRISK. Dietary patterns did not add predictive value. Sensitivity analysis excluding subjects with prediabetes at baseline confirmed these results. In addition, an association between baseline consumption of high-fiber foods with incident T2D emerged, suggesting a different behaviour between healthy and prediabetic subjects.

conclusionsBaseline circulating concentrations of SCFAs are associated with high-fiber food consumption and independently predict the development of T2D over seven years of follow-up. However, they offer limited improvement in risk prediction compared to traditional risk factors, though they enhance risk prediction as assessed by FINDRISK. Further studies are necessary to evaluate the impact of dietary interventions on SCFA.

Indexed as

Diabetes Mellitus, Type 2Diet, MediterraneanFatty Acids, VolatileAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsSpainFatty Acids, VolatileHigh-fiber food consumptionMediterranean DietRisk predictionShort-chain fatty acidsType 2 diabetes mellitus

Identifiers

PMID40481510
PMCPMC12143092

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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.