Evidence map›Paper›PMID 34133768›Full record

Trial reportHepatology (Baltimore, Md.)2021

Chyme Reinfusion Restores the Regulatory Bile Salt-FGF19 Axis in Patients With Intestinal Failure.

Kiran V K Koelfat, Denis Picot, Xinwei Chang, Mireille Desille-Dugast, Hans M van Eijk, Sander M J van Kuijk, Martin Lenicek, Sabrina Layec, Marie Carsin, Laurence Dussaulx and 6 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02990195 (Restoring the Beneficial Effects of Enterohepatic Bile Salt Signalling by Chyme Reinfusion in Patients With a Double Enterostomy), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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.

NCT02990195 phase2completednot on this map

Restoring the Beneficial Effects of Enterohepatic Bile Salt Signalling by Chyme Reinfusion in Patients With a Double Enterostomy

TypeinterventionalSponsorRennes University HospitalRan2016 to 2018Enrolled13ConditionsDouble EnterostomyArmsChyme reinfusion
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. FGF-based drug discovery: advances and challenges.Nature reviews. Drug discovery · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. 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

16 authors at 5 institutions in 4 countries.

Kiran V K Koelfat *Department of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.ORCID 0000-0002-5209-6775
Denis Picot *Department of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Xinwei Chang *Department of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.
Mireille Desille-DugastINSERM, INRAE, University of Rennes, Nutrition Metabolisms and Cancer, NuMeCan, Nutrition Unit, CRB Santé, CHU Rennes, Rennes, France.
Hans M van EijkDepartment of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.
Sander M J van KuijkDepartment of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Center, Maastricht, the Netherlands.
Martin LenicekInstitute of Medical Biochemistry and Laboratory Diagnostics, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
Sabrina LayecDepartment of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Marie CarsinDepartment of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Laurence DussaulxDepartment of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Eloi SeynhaeveDepartment of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Florence TrivinDepartment of Nutritional and Digestive Rehabilitation, Clinique Saint Yves, Rennes, France.
Laurence LacazeINSERM, INRAE, University of Rennes, Nutrition Metabolisms and Cancer, NuMeCan, Nutrition Unit, CRB Santé, CHU Rennes, Rennes, France.
Ronan Thibault *INSERM, INRAE, University of Rennes, Nutrition Metabolisms and Cancer, NuMeCan, Nutrition Unit, CRB Santé, CHU Rennes, Rennes, France.
Frank G Schaap *Department of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.ORCID 0000-0002-1597-572X
Steven W M Olde Damink *Department of Surgery, Maastricht University Medical Center, Maastricht, the Netherlands.
Yves Rocher (France) · FRMaastricht University · NLInserm · FRCharles University · CZMaastricht University Medical Centre · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsAutomated chyme reinfusion (CR) in patients with intestinal failure (IF) and a temporary double enterostomy (TDE) restores intestinal function and protects against liver injury, but the mechanisms are incompletely understood. The aim was to investigate whether the beneficial effects of CR relate to functional recovery of enterohepatic signaling through the bile salt-FGF19 axis. APPROACH AND

resultsBlood samples were collected from 12 patients, 3 days before, at start, and 1, 3, 5, and 7 weeks after CR initiation. Plasma FGF19, total bile salts (TBS), 7-α-hydroxy-4-cholesten-3-one (C4; a marker of bile salt synthesis), citrulline (CIT), bile salt composition, liver tests, and nutritional risk indices were determined. Paired small bowel biopsies prior to CR and after 21 days were taken, and genes related to bile salt homeostasis and enterocyte function were assessed. CR induced an increase in plasma FGF19 and decreased C4 levels, indicating restored regulation of bile salt synthesis through endocrine FGF19 action. TBS remained unaltered during CR. Intestinal farnesoid X receptor was up-regulated after 21 days of CR. Secondary and deconjugated bile salt fractions were increased after CR, reflecting restored microbial metabolism of host bile salts. Furthermore, CIT and albumin levels gradually rose after CR, while abnormal serum liver tests normalized after CR, indicating restored intestinal function, improved nutritional status, and amelioration of liver injury. CR increased gene transcripts related to enterocyte number, carbohydrate handling, and bile salt homeostasis. Finally, the reciprocal FGF19/C4 response after 7 days predicted the plasma CIT time course.

conclusionsCR in patients with IF-TDE restored bile salt-FGF19 signaling and improved gut-liver function. Beneficial effects of CR are partly mediated by recovery of the bile salt-FGF19 axis and subsequent homeostatic regulation of bile salt synthesis.

Indexed as

Gastrointestinal ContentsAgedAged, 80 and overAnastomosis, SurgicalBile Acids and SaltsEnteral NutritionEnterostomyFemaleFibroblast Growth FactorsHumansIntestinal FailureMaleMiddle AgedNutritional StatusProspective StudiesTreatment OutcomeBile Acids and SaltsFGF19 protein, humanFibroblast Growth Factors

Identifiers

PMID34133768
PMCPMC8596508
OpenAlexW3171731789

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LicenceCC BY-NC-ND
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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.