Evidence map›Paper›PMID 42616205›Full record

ArticleArchives of osteoporosis2026

Long-term effects of denosumab: a 10-year single-center retrospective study.

Federico Aldegheri, Matteo Appoloni, Nicolò Passoni, Vittorio Zibordi, Maurizio Rossini, Davide Gatti, Giovanni Adami, Francesco Pollastri, Angelo Fassio, Ombretta Viapiana

Abstract read
In one paragraph

Article in Archives of osteoporosis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Federico AldegheriRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy. federico.aldegheri@univr.it.ORCID http://orcid.org/0009-0005-3965-5295
Matteo AppoloniRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0009-0004-5134-1304
Nicolò PassoniRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.
Vittorio ZibordiRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0009-0004-4389-1322
Maurizio RossiniRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0000-0001-9692-2293
Davide GattiRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0000-0002-7471-3076
Giovanni AdamiRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0000-0002-8915-0755
Francesco PollastriRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0009-0006-1691-2196
Angelo FassioRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0000-0001-9187-232X
Ombretta ViapianaRheumatology Unit, Department of Medicine, University of Verona, Pz Scuro 10, 37134, Verona, Italy.ORCID http://orcid.org/0000-0003-1917-5655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis weakens bones and increases the risk of fractures. Denosumab is a medication that reduces bone loss and increases bone mineral density (BMD). In this real-world study, we followed patients who received denosumab every 6 months for 10 years. We found that bone density continued to improve throughout treatment. People who had taken bisphosphonates before starting denosumab responded just as well in the long term. Blood tests showed stable reduction of bone turnover markers.

backgroundDenosumab produces durable BMD gains and low fracture rates in clinical trials, but long-term real-world evidence is limited, especially on the effect of prior bisphosphonate exposure and characteristics of patients who fracture during therapy.

methodsWe conducted a 10-year single-center real-world retrospective study including patients receiving continuous denosumab 60 mg every 6 months. Clinical, biochemical, and densitometric data were extracted from an institutional electronic database. Longitudinal changes in BMD at total hip, lumbar spine, and femoral neck were analyzed using linear mixed-effects models adjusted for baseline BMD, age, baseline severe vertebral fractures, and glucocorticoid exposure. Bone turnover markers (CTX, ALP, PTH) were analyzed with mixed-effects models adjusted for renal function.

resultsA total of 145 patients were included (mean age 70.9 years; 95.9% women). Over 10 years, BMD increased significantly at all skeletal sites: +12.9% at the total hip, + 16.3% at the lumbar spine, and +6.0% at the femoral neck. CTX and ALP showed marked and sustained reduction, whereas PTH remained stable over time. Prior bisphosphonate exposure did not modify long-term BMD trajectories at any site, and group differences in CTX converged after treatment initiation. Patients who sustained fractures showed significantly attenuated lumbar spine BMD gains, while hip sites displayed similar trajectories to non-fractured patients.

conclusionsIn a real-world setting, continuous denosumab therapy for 10 years produced robust and sustained BMD gains, accompanied by a durable and stable reduction in bone turnover. Prior bisphosphonate exposure influenced only early biochemical differences and did not affect decade-long BMD responses.

Indexed as

Bone DensityBone Density Conservation AgentsDenosumabOsteoporosisAgedAged, 80 and overBone RemodelingDiphosphonatesFemaleHumansLumbar VertebraeMaleMiddle AgedRetrospective StudiesTreatment OutcomeBone Density Conservation AgentsDenosumabDiphosphonatesBisphosphonatesBone mineral densityDenosumabFracture riskLong-term therapyOsteoporosisReal-world evidence

Identifiers

PMID42616205
PMCPMC13490209

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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.