Evidence map›Paper›PMID 41159664›Full record

ArticleMolecular nutrition & food research2025

Microbial Transformation of Dietary Glycerol Contributes to Intestinal Acrolein Formation and Urinary Excretion.

Clarissa Schwab, Hanna Lang, Simone Stegmüller, Jiri Hosek, Angeliki Marietou, Lucia Huertas-Díaz, Qing Li, Asta Petrine Smedgaard Krings, Andrea Zander, Ulrik Kræmer Sundekilde and 1 more

Abstract read
In one paragraph

Article in Molecular nutrition & food research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Clarissa SchwabDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Hanna LangDivision of Food Chemistry and Toxicology, Department of Chemistry, RPTU University Kaiserslautern-Landau, Kaiserslautern, Germany.
Simone StegmüllerDivision of Food Chemistry and Toxicology, Department of Chemistry, RPTU University Kaiserslautern-Landau, Kaiserslautern, Germany.
Jiri HosekDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Angeliki MarietouDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Lucia Huertas-DíazDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Qing LiDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Asta Petrine Smedgaard KringsDepartment of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Andrea ZanderDivision of Food Chemistry and Toxicology, Department of Chemistry, RPTU University Kaiserslautern-Landau, Kaiserslautern, Germany.
Ulrik Kræmer SundekildeDepartment of Food Science, Aarhus University, Aarhus, Denmark.
Elke RichlingDivision of Food Chemistry and Toxicology, Department of Chemistry, RPTU University Kaiserslautern-Landau, Kaiserslautern, Germany.

Funding

Deutsche Forschungsgemeinschaft DFG RI 1176/12-1Deutsche Forschungsgemeinschaft DFG RI 1176/13-1
6 · The paper itself

Abstract

The aldehyde acrolein has been associated with diabetes, cardiovascular, respiratory, and neurodegenerative diseases, and gut microbiota possesses the potential for acrolein release via the key enzyme glycerol/diol dehydratase (PduCDE). This study aimed at estimating the contribution of gut microbiota to endogenous acrolein production. To minimize confounding sources, we investigated the intestinal acrolein-producing potential of 20 volunteers housed under defined conditions. Glycerol was present in every meal and was detected in feces, suggesting availability to intestinal microbiota. Based on fecal metagenomics and pduC analysis, all volunteers showed potential for intestinal glycerol transformation to acrolein; the genus Anaerobutyricum was the major contributor across donors and time. Levels of urine biomarkers N-acetyl-S-(3-hydroxypropyl)-L-cysteine (3-HPMA) and N-acetyl-S-(carboxyethyl)-L-cysteine (CEMA) were higher after the consumption of meals with high glycerol levels, suggesting immediate microbial transformation to acrolein. Only a small proportion of acrolein metabolites was recovered in urine, possibly due to high compound reactivity. Donors could be separated into 3-HPMA or CEMA phenotypes based on the predominance of urine biomarkers, and phenotypes related to overall fecal microbiota and fermentation metabolite profiles. Our data show that oral fat/glycerol intake together with intestinal microbiota activity might temporarily increase endogenous acrolein formation and that urinary biomarkers link to the intestinal microbiome.

Indexed as

AcroleinGastrointestinal MicrobiomeGlycerolIntestinesAcetylcysteineAdultBiomarkersDietFecesFemaleHumansMaleMiddle AgedYoung AdultAcetylcysteineAcroleinBiomarkersGlycerolS-(3-hydroxypropyl)cysteine N-acetate3‐HPMACEMAdietglycerolgut microbiota

Identifiers

PMID41159664
PMCPMC12700045

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Registered trials

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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.