Evidence map›Paper›PMID 42438428›Full record

ArticleUnited European gastroenterology journal2026

Clinical and Mechanistic Association Between Intestinal Permeability and the Gut Microbiome in Cirrhosis: Role of Phascolarctobacterium.

Rosa Haller, Nicole Feldbacher, Stefan Fürst, Johannes Woltsche, Lukas Gulden, Jakob Schwarzl, Julia Traub, Tobias Madl, Hansjörg Habisch, Angela Horvath and 1 more

2 registry-linked trialsAbstract read
In one paragraph

Article in United European gastroenterology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

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

NCT01607528 nacompletednot on this map

Probiotic Modulation of Gut Microflora in Cirrhosis: Influence on Immune Function and Infections

TypeinterventionalSponsorMedical University of GrazRan2012 to 2014Enrolled92ConditionsLiver CirrhosisArmsWinclove-849, Placebo
NCT03080129 narecruitingnot on this map

Microbiome and Sarcopenia in Patients With Liver Cirrhosis: A Prospective Controlled Cohort Study

TypeinterventionalSponsorMedical University of GrazRan2017 to 2026Enrolled120ConditionsSarcopenia, Liver CirrhosisArmsFresubin energy
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

11 authors.

Rosa HallerDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID https://orcid.org/0009-0008-4899-3802
Nicole FeldbacherDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Stefan FürstDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Johannes WoltscheDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID https://orcid.org/0000-0002-2240-6736
Lukas GuldenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Jakob SchwarzlDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Julia TraubDepartment of Clinical Medical Nutrition, University Hospital Graz, Graz, Austria.
Tobias MadlOtto Loewi Research Center, Medicinal Chemistry, Medical University of Graz, Graz, Austria.ORCID https://orcid.org/0000-0002-9725-5231
Hansjörg HabischOtto Loewi Research Center, Medicinal Chemistry, Medical University of Graz, Graz, Austria.
Angela HorvathDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Vanessa StadlbauerDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.

Funding

Austrian Infrastructure Program 2016/2017Austrian Science Fund 10.55776/COE14Austrian Science Fund 10.55776/DOC130Austrian Science Fund 10.55776/I3792Austrian Science Fund 10.55776/P28854Austrian Science Fund 10.55776/W1226Austrian Science Fund KLI 741Austrian Science Fund KLIF-741 B34BioTechMed-GrazCity of GrazDoctoral program MOLMEDIntegrative Metabolism Research Center GrazÖsterreichische ForschungsförderungsgesellschaftStyrian Government; Zukunftsfonds; doc.fund program
6 · The paper itself

Abstract

backgroundIn patients with liver cirrhosis, intestinal permeability and the composition of the gut microbiome are altered. Thus, the microbiome might be a therapeutic target for the treatment of both liver diseases and intestinal permeability. We aimed to investigate the relationship between the intestinal barrier and microbiome composition in cirrhosis and elucidate potential mechanisms for how bacteria influence permeability.

methodsWe analyzed the fecal permeability biomarker zonulin by ELISA and microbiome composition by 16s rDNA sequencing in a discovery (n = 78) and a validation cohort (n = 90) of patients with liver cirrhosis. In the validation cohort, we analyzed the composition of the fecal metabolome by NMR spectroscopy. For mechanistic exploration, an intestinal barrier cell culture model using T84 cells was used.

resultsIn the discovery cohort (n = 78, 77% Child-Pugh Grade A, 21% Child-Pugh Grade B, 3% Child-Pugh Grade C), decreasing zonulin levels in stool over 6 months were associated with higher Phascolarctobacterium abundance in the microbiome. Phascolarctobacterium was associated with better liver function (lower bilirubin, p = 0.04, INR p = 0.04, MELD Score, p = 0.02). Lower Phascolarctobacterium levels were observed in decompensated cirrhosis and were associated with 36-month mortality in two cohorts. Metabolomics analysis showed an association between Phascolarctobacterium and lower succinate levels. Succinate increased gut permeability in vitro, and Phascolarctobacterium succinatutens strains improved the intestinal permeability, potentially by alleviating the effect of succinate.

conclusionPhascolarctobacterium may represent a candidate biomarker of adverse outcomes in cirrhosis and a promising target for further investigation as a next-generation probiotic involved in gut barrier function and succinate homeostasis.

trial registrationNCT01607528, NCT03080129.

Indexed as

Gastrointestinal MicrobiomeIntestinal MucosaLiver CirrhosisAgedBiomarkersCholera ToxinFecesFemaleHaptoglobinsHumansIntestinal Barrier FunctionMagnetic Resonance SpectroscopyMaleMiddle AgedPermeabilityProtein PrecursorsBiomarkersCholera ToxinHaptoglobinsProtein PrecursorsRNA, Ribosomal, 16Szonulingut‐liver axisgut metabolomeintestinal barriersuccinatezonulin

Identifiers

PMID42438428
PMCPMC13358567

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Registered trials

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.