Evidence map›Paper›PMID 31687645›Full record

ArticleJBMR plus2019

A Pilot Study Showing Acute Inhibitory Effect of GLP-1 on the Bone Resorption Marker CTX in Humans.

Anne Nissen, Simone Marstrand, Kirsa Skov-Jeppesen, Lasse Bremholm, Mads Hornum, Ulrik B Andersen, Jens Juul Holst, Mette Marie Rosenkilde, Bolette Hartmann

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
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  5. Article
  6. Article
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  10. Article
  11. The Gut-Bone Axis in Diabetes.Current osteoporosis reports · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. A quinoxaline-based compound ameliorates bone loss in ovariectomized mice.Experimental biology and medicine (Maywood, N.J.) · 2021
    Article
  17. Article
  18. Review
  19. The Effect of Inflammation on Bone.Frontiers in physiology · 2020
    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

9 authors at 1 institution in 1 country.

Anne NissenDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.ORCID https://orcid.org/0000-0001-9790-7642
Simone MarstrandDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.
Kirsa Skov-JeppesenDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.
Lasse BremholmDepartment of Surgery (Gastroenterology Section) Zealand University Hospital, University of Copenhagen Copenhagen Denmark.
Mads HornumDepartment of Nephrology Rigshospitalet Copenhagen Denmark.
Ulrik B AndersenDepartment of Clinical Physiology and Nuclear Medicine and PET Rigshospitalet (Glostrup Section), University of Copenhagen Copenhagen Denmark.
Jens Juul HolstDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.
Mette Marie RosenkildeDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.
Bolette HartmannDepartment of Biomedical Sciences The Panum Institute, University of Copenhagen Copenhagen Denmark.ORCID https://orcid.org/0000-0001-8509-2036
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bones have been suggested to be a target for glucagon-like peptide -1 (GLP-1); however, studies of the effects on human bones so far have given diverging results. We hypothesized that GLP-1, together with glucagon-like peptide-2 and glucose-dependent insulinotropic polypeptide, plays a role in the gut-bone axis. We examined the acute effect of three GLP-1 receptor ligands [GLP-1 (7-36)amide, GLP-1 (9-36)amide, and exenatide] on markers of bone remodeling. Eight healthy, normal-weight participants, with a mean age of 24.3 years, were studied for 4 days in a double-blinded, randomized clinical trial. Blood was collected before and after s.c. injection of GLP-1 (7-36)amide (1.5 nmol/kg), GLP-1 (9-36)amide (1.5 nmol/kg), exenatide (2.4 nmol/subject), or saline. Plasma was analyzed for bone markers and for osteoprotegerin (OPG), PTH, and IGF-1 levels. All ligands were tested in vitro for their cAMP-inducing activity on the human GLP-1 receptor. GLP-1 (7-36)amide decreased CTX-levels, compared with placebo (area under the curve [AUC] ±SD 0 to 120 min = -2143 ± 1294 % × min versus -883 ± 1557 % × min;

Indexed as

BONE REMODELINGBONE RESORPTIONCTXEXENATIDEGLUCAGON‐LIKE PEPTIDE‐1

Identifiers

PMID31687645
PMCPMC6820456
OpenAlexW2951518622

What OpenQuestion 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 OpenQuestion graph.