Evidence map›Paper›PMID 28202805›Full record

Trial reportPhysiological reports2017

Chenodeoxycholic acid stimulates glucagon-like peptide-1 secretion in patients after Roux-en-Y gastric bypass.

Signe Nielsen, Maria S Svane, Rune E Kuhre, Trine R Clausen, Viggo B Kristiansen, Jens F Rehfeld, Jens J Holst, Sten Madsbad, Kirstine N Bojsen-Moller

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Physiological reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.0field-weighted citation impact, top 3% 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.

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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Redox-Dependent Effects in the Physiopathological Role of Bile Acids.Oxidative medicine and cellular longevity · 2021
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Chenodeoxycholic Acid Ameliorates AlClMolecules (Basel, Switzerland) · 2019
    Article
  16. Review
  17. Article
  18. Article
  19. Mechanisms in bariatric surgery: Gut hormones, diabetes resolution, and weight loss.Surgery for obesity and related diseases : official journal of the American Society for Bariatric Surgery · 2018
    Article
  20. 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

9 authors at 4 institutions in 1 country.

Signe NielsenDepartment of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Maria S SvaneDepartment of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Rune E KuhreNNF Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
Trine R ClausenObesity Biology, Novo Nordisk A/S, Maaloev, Denmark.
Viggo B KristiansenDepartment of Surgical Gastroenterology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Jens F RehfeldDepartment of Clinical Biochemistry, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Jens J HolstNNF Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark.
Sten MadsbadDepartment of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
Kirstine N Bojsen-MollerDepartment of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark kirstine.bojsen-moeller@regionh.dk.ORCID http://orcid.org/0000-0003-1962-5302
University of Copenhagen · DKCopenhagen University Hospital · DKHvidovre Hospital · DKNovo Nordisk (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Postprandial secretion of glucagon-like peptide-1 (GLP-1) is enhanced after Roux-en-Y gastric bypass (RYGB), but the precise molecular mechanisms explaining this remain poorly understood. Plasma concentrations of bile acids (BAs) increase after RYGB, and BAs may act as molecular enhancers of GLP-1 secretion through activation of TGR5-receptors. We aimed to evaluate GLP-1 secretion after oral administration of the primary bile acid chenodeoxycholic acid (CDCA) and the secondary bile acid ursodeoxycholic acid (UDCA) (which are available for oral use) in RYGB-operated participants. Eleven participants (BMI 29.1 ± 1.2, age 37.0 ± 3.2 years, time from RYGB 32.3 ± 1.1 months, weight loss after RYGB 37.0 ± 3.1 kg) were studied in a placebo-controlled, crossover-study. On three different days, participants ingested (1) placebo (water), (2) UDCA 750 mg, (3) CDCA 1250 mg (highest recommended doses). Oral intake of CDCA increased plasma concentrations of GLP-1, C-peptide, glucagon, peptide YY, neurotensin, total bile acids, and fibroblast growth factor 19 significantly compared with placebo (all

Indexed as

Gastric BypassAdministration, OralAdultBile Acids and SaltsBlood GlucoseChenodeoxycholic AcidC-PeptideCross-Over StudiesFemaleFibroblast Growth FactorsGlucagonGlucagon-Like Peptide 1HumansMaleUrsodeoxycholic AcidBile Acids and SaltsBlood GlucoseChenodeoxycholic AcidC-PeptideFGF19 protein, humanFibroblast Growth FactorsGlucagonGlucagon-Like Peptide 1Ursodeoxycholic AcidBile acidsGLP‐1PYYRoux‐en‐Y gastric bypass

Identifiers

PMID28202805
PMCPMC5309580
OpenAlexW2588731317

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.