Evidence map›Paper›PMID 38737002›Full record

ArticleEClinicalMedicine2024

Once-weekly semaglutide versus placebo in adults with increased fracture risk: a randomised, double-blinded, two-centre, phase 2 trial.

Morten S Hansen, Eva M Wölfel, Shakespeare Jeromdesella, Jens-Jakob K Møller, Charlotte Ejersted, Niklas R Jørgensen, Richard Eastell, Stinus G Hansen, Morten Frost

Registry-linked trialAbstract read
In one paragraph

Article in EClinicalMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04702516 (The Effect of Semaglutide), which is not on this map. Cited by 56 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 3 pooled it
–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.

NCT04702516 phase1 / phase2unknown statusnot on this map

The Effect of Semaglutide (Ozempic) on Bone Turnover in Patients With Increased Fracture Risk: a Randomized Placebo-controlled Clinical Trial

TypeinterventionalSponsorMorten FrostRan2021 to 2022Enrolled64ConditionsOsteopeniaArmsOzempic, Placebo
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  17. Obesity-related bone fragility: An emerging clinical paradox.The Indian journal of medical research · 2026
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  19. Lower fall and femoral fracture risks with semaglutide and tirzepatide compared with DPP-4 inhibitors in older adults with type 2 diabetes.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
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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.

Morten S HansenDepartment of Endocrinology, Odense University Hospital, Denmark.
Eva M WölfelClinical Institute, Faculty of Health Sciences, University of Southern Denmark, Denmark.
Shakespeare JeromdesellaDepartment of Endocrinology, Odense University Hospital, Denmark.
Jens-Jakob K MøllerOpen Patient Data Explorative Network (OPEN), Odense University Hospital, Denmark.
Charlotte EjerstedDepartment of Endocrinology, Odense University Hospital, Denmark.
Niklas R JørgensenDepartment of Clinical Biochemistry, Rigshospitalet, Denmark.
Richard EastellDivision of Clinical Medicine, University of Sheffield, Sheffield, United Kingdom.
Stinus G HansenDepartment of Diabetes and Endocrinology, Esbjerg Hospital, University Hospital of Southern Denmark, Denmark.
Morten FrostDepartment of Endocrinology, Odense University Hospital, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Previous studies have indicated that glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1RAs) may enhance bone formation and have neutral or beneficial effects on fracture risk. We evaluated the effect of the GLP-1RA semaglutide on the bone formation marker Procollagen type I N-terminal propeptide (PINP) in adults with increased fracture risk. Methods: This randomised, placebo-controlled, double-blinded, phase 2 clinical trial was conducted at two public hospitals in Denmark. We enrolled 64 men and women with increased fracture risk based on a T-score < -1.0 at the total hip or lumbar spine and/or low-energy fracture within three years of recruitment. Participants were randomised (1:1) to receive once-weekly subcutaneous semaglutide 1.0 mg or placebo. The primary outcome was changes in plasma (P)-PINP from baseline to week 52. Primary and safety outcomes were assessed and evaluated for all participants. This trial is complete and registered with ClinicalTrials.gov, NCT04702516. Findings: Between March 24 and December 8, 2021, 55 (86%) postmenopausal women and nine men with a mean age of 63 years (SD 5.5) and BMI of 27.5 kg/m Interpretation: In adults with increased fracture risk, semaglutide once weekly did not increase bone formation based on the bone formation marker P-PINP. The observed increase in bone resorption in the semaglutide group may be explained by the accompanying weight loss. Funding: Region of Southern Denmark, Novo Nordisk Foundation, and Gangsted Foundation. Novo Nordisk provided the investigational drug and placebo.

Indexed as

Bone turnoverCortical boneSemaglutideWeight loss

Identifiers

PMID38737002
PMCPMC11087719

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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.