Evidence map›Paper›PMID 42883965›Full record

ArticleInternational journal of molecular sciences2026

Cranberry Extract and Polyphenol Metabolites Modulate Luminal and Mucosal Microbiome.

Frank H J Schuren, Mirna Baak, Noemie Daniel, Bowien van Leijden, Barbara Vanhoecke, Alexandra Meynier, Margreet Heerikhuisen, Séverine Méance, Maria Wiese

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Frank H J SchurenMicrobiology and Systems Biology, TNO The Netherlands Organization for Applied Scientific Research, 2333 BE Leiden, The Netherlands.ORCID 0000-0001-6982-5340
Mirna BaakMicrobiology and Systems Biology, TNO The Netherlands Organization for Applied Scientific Research, 2333 BE Leiden, The Netherlands.
Noemie DanielHealth Active Solutions, Symrise, 35000 Rennes, France.ORCID 0000-0003-4319-0054
Bowien van LeijdenMicrobiology and Systems Biology, TNO The Netherlands Organization for Applied Scientific Research, 2333 BE Leiden, The Netherlands.
Barbara VanhoeckeGlobal Research and Innovation, Metagenics, 8400 Oostende, Belgium.
Alexandra MeynierNutrition Research, Mondelez, 91400 Saclay, France.ORCID 0000-0002-9567-0351
Margreet HeerikhuisenMicrobiology and Systems Biology, TNO The Netherlands Organization for Applied Scientific Research, 2333 BE Leiden, The Netherlands.
Séverine MéanceHealth Active Solutions, Symrise, 35000 Rennes, France.
Maria WieseMicrobiology and Systems Biology, TNO The Netherlands Organization for Applied Scientific Research, 2333 BE Leiden, The Netherlands.

Funding

Health Holland
6 · The paper itself

Abstract

Cranberry polyphenols (PPs) are associated with various health benefits, which can be exerted by the known parent compounds and/or through related metabolites resulting from microbial metabolization. Metabolite levels and profile/composition are often subject to extensive inter-individual variability, and many aspects of the relevant bidirectional interactions of PPs with the individual gut microbiota are still elusive. Both undigested and predigested cranberry extract were tested, next to procyanidin A2 and hyperoside controls, on the luminal and mucosa-associated gut microbial communities of six healthy adult donors in vitro. The composition of the microbial communities, polyphenolic substrate metabolization patterns, and microbial metabolites, including short-chain fatty acids (SCFAs), bile acids and aromatic acids, were analyzed at different timepoints. Both predigested and undigested cranberry extracts modulated the microbiota composition in all donors, albeit with individual variations. The mucosal samples responded differently than the luminal samples, and the type of extract also affected the composition of microbiota differently. Further, inter-individual differences in the metabolization patterns and metabolite production, such as 3,4 DHPPA (3,4-dihydroxyphenylpropionic acid), 3,4 DHPP-2-ol, and 3,4-dihydroxyphenyl acetic acid, were observed. SCFA production was stimulated with predigested cranberry extract. A semipolar compound analysis further showed much broader metabolic variations, both in cranberry-related metabolites, such as 4-vinylphenol and 3,4,5-trimethoxyphenylacetic acid, and in microbial metabolites such as indole-3-lactic acid. This study increases the knowledge on how individual microbiota samples are modulated upon exposure to cranberry-related PPs and how this influences their metabolic activity.

Indexed as

Gastrointestinal MicrobiomeMicrobiotaPlant ExtractsPolyphenolsVaccinium macrocarponAdultFatty Acids, VolatileHumansMaleFatty Acids, VolatilePlant ExtractsPolyphenolscranberry extractin vitrometabolitesmucosal and luminal microbiotapolyphenols

Identifiers

PMID42883965
PMCPMC13664764

What OpenQuestion holds

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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.