Evidence map›Paper›PMID 34579074›Full record

Trial reportNutrients2021

Associations between Postprandial Gut Hormones and Markers of Bone Remodeling.

Nina Wittorff Jensen, Kim Katrine Bjerring Clemmensen, Marie Møller Jensen, Hanne Pedersen, Kristine Færch, Lars Jorge Diaz, Jonas Salling Quist, Joachim Størling

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

8 authors at 2 institutions in 1 country.

Nina Wittorff JensenClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.
Kim Katrine Bjerring ClemmensenClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.ORCID 0000-0002-4530-1945
Marie Møller JensenClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.ORCID 0000-0003-2660-3240
Hanne PedersenClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.ORCID 0000-0001-7913-7373
Kristine FærchClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.ORCID 0000-0002-6127-0448
Lars Jorge DiazClinical Epidemiology Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.
Jonas Salling QuistClinical Prevention Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.ORCID 0000-0001-6036-0962
Joachim StørlingDepartment of Biomedical Sciences, University of Copenhagen, 1165 Copenhagen, Denmark.
Steno Diabetes Centers · DKUniversity of Copenhagen · DK

Funding

Novo Nordisk Fonden NNF17OC0027822
6 · The paper itself

Abstract

Gut-derived hormones have been suggested to play a role in bone homeostasis following food intake, although the associations are highly complex and not fully understood. In a randomized, two-day cross-over study on 14 healthy individuals, we performed postprandial time-course studies to examine the associations of the bone remodeling markers carboxyl-terminal collagen type I crosslinks (CTX) and procollagen type 1 N-terminal propeptide (P1NP) with the gut hormones glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide 1 (GLP-1), and peptide YY (PYY) using two different meal types-a standardized mixed meal (498 kcal) or a granola bar (260 kcal). Plasma concentrations of total GIP, total GLP-1, total PYY, CTX, and P1NP were measured up to 240 min after meal intake, and the incremental area under the curve (iAUC) for each marker was calculated. The iAUC of CTX and P1NP were used to assess associations with the iAUC of GIP, GLP-1, and PYY in linear mixed effect models adjusted for meal type. CTX was positively associated with GIP and GLP-1, and it was inversely associated with PYY (all

Indexed as

Postprandial PeriodArea Under CurveBiomarkersBone and BonesBone RemodelingBone ResorptionCollagen Type ICross-Over StudiesEatingFemaleGastric Inhibitory PolypeptideGastrointestinal HormonesGlucagon-Like Peptide 1Healthy VolunteersHomeostasisHumansBiomarkersCollagen Type Icollagen type I trimeric cross-linked peptideGastric Inhibitory Polypeptidegastric inhibitory polypeptide receptorGastrointestinal HormonesGlucagon-Like Peptide 1Peptide FragmentsPeptidesPeptide YYProcollagenprocollagen Type I N-terminal peptideReceptors, Gastrointestinal Hormonebone markersbone metabolismCTXgut hormonesP1NP

Identifiers

PMID34579074
PMCPMC8467604
OpenAlexW3200443954

What Socratic holds

Textmetadata
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.