Evidence map›Paper›PMID 39623217›Full record

Observational studyOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2025

Bisphosphonate drug holidays in osteoporosis according to fracture risk profile.

Asunción Salmoral, P Peris, C López Medina, H Flórez, M Barceló, M Pascual Pastor, I Ros, D Grados, P Aguado, S García and 13 more

Abstract readObservational StudyMulticenter Study
PubMed Publisher
In one paragraph

Observational study in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2025. 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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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

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5 · Who and what money

Authors and funding

23 authors.

Asunción SalmoralDepartment of Rheumatology, University Hospital Reina Sofía, Maimonides Institute for Biomedical Research of Córdoba (IMIBIC), University of Córdoba, Cordoba, Spain. asuncionsalmoral61@gmail.com.ORCID http://orcid.org/0009-0004-8097-7846
P PerisDepartment of Rheumatology, Hospital Clínic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
C López MedinaDepartment of Rheumatology, University Hospital Reina Sofía, Maimonides Institute for Biomedical Research of Córdoba (IMIBIC), University of Córdoba, Cordoba, Spain.
H FlórezDepartment of Rheumatology, Hospital Clínic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
M BarcelóDepartment of Rheumatology, Rheumatology Research Group, Vall d'Hebron Research Institute, University Hospital Vall d´Hebron of Barcelona, Barcelona, Spain.
M Pascual PastorDepartment of Rheumatology, Rheumatology Research Group, Vall d'Hebron Research Institute, University Hospital Vall d´Hebron of Barcelona, Barcelona, Spain.
I RosDepartment of Rheumatology, University Hospital Son Llàtzer, Palma de Mallorca, Spain.
D GradosDepartment of Rheumatology, University Hospital d' Igualada, Barcelona, Spain.
P AguadoDepartment of Rheumatology, University La Paz, Madrid, Spain.
S GarcíaDepartment of Rheumatology, University La Paz, Madrid, Spain.
L LópezDepartment of Rheumatology, Hospital Sant Rafael, Barcelona, Spain.
L GifreDepartment of Rheumatology, University Hospital Germans Trias, Badalona, Spain.
D CerdáDepartment of Rheumatology, Hospital Moisès Broggi, Sant Joan Despí, University of Barcelona, Barcelona, Spain.
F J AguilarDepartment of Rheumatology, University Hospital Virgen de La Victoria, Málaga, Spain.
B PaneroDepartment of Rheumatology, University Hospital Virgen de La Victoria, Málaga, Spain.
E CostaDepartment of Rheumatology, University Hospital Parc Taulí, Sabadell, Spain.
E CasadoDepartment of Rheumatology, University Hospital Parc Taulí, Sabadell, Spain.
B HernándezDepartment of Rheumatology, University Hospital Virgen Macarena, Sevilla, Spain.
A Martínez FerrerDepartment of Rheumatology, University Hospital Dr Peset, Valencia, Spain.
J GrañaDepartment of Rheumatology, University Hospital of A Coruña, Institute for Biomedical Research of A Coruña (INIBIC), A Coruña, Spain.
I GómezDepartment of Rheumatology, University Hospital Reina Sofía, Maimonides Institute for Biomedical Research of Córdoba (IMIBIC), University of Córdoba, Cordoba, Spain.
N GuañabensDepartment of Rheumatology, Hospital Clínic, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
OsteoResSer Working Group of the Spanish Society of Rheumatology

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We analyzed the incidence of fractures and changes in bone mineral density and bone turnover markers in 264 patients who discontinued bisphosphonates. Fractures were recorded in 12.3%. Half were clinical vertebral fractures. We identified patients with a high-risk profile who should not discontinue treatment.

objectiveThe optimal length of bisphosphonate discontinuation is unknown, as is the type of patient who could benefit from this approach. The objectives of the study were to analyze, in clinical practice, the incidence of fractures and associated risk factors, changes in bone mineral density (BMD) and bone turnover markers (BTMs) after discontinuation of bisphosphonates.

methodsThis observational retrospective study included 264 patients from 14 Spanish rheumatology departments. Postmenopausal women or men with osteoporosis received alendronate or risedronate for ≥ 5 years or zoledronate for ≥ 3 years and had discontinued treatment for ≥ 1 year or ≥ 2 years, respectively. Spinal X-rays were obtained before discontinuation and in suspected clinical vertebral fracture during follow-up. BMD and BTMs were determined before discontinuation and at different time points.

resultsThe mean discontinuation time was 2.7 (± 6.7) years. Thirty-two patients (12.3%) had 36 fractures, mainly clinical vertebral fractures. The main risk factor for fracture was a high-risk profile (femoral neck T-score ≤ -2.5 and/or a history of fracture and/or multiple fractures [≥ 5 years]) before discontinuation. At 12 months, 10.41% of patients with high-risk profile experienced a fracture, being 0.8% and 1.08% in moderate- and low-risk patients, respectively. Significant BMD loss at the femoral neck and total hip was detected, with duration of discontinuation being the key factor. PINP was the marker with the greatest changes.

conclusionsWe identified a profile of patients with osteoporosis who should not discontinue bisphosphonates, owing to the possibility of fractures, especially vertebral, which are already evident the first year after discontinuation.

Indexed as

Bone Density Conservation AgentsDiphosphonatesOsteoporosisOsteoporotic FracturesAgedAged, 80 and overBiomarkersBone DensityBone RemodelingDrug Administration ScheduleFemaleHumansIncidenceLumbar VertebraeMaleMiddle AgedBiomarkersBone Density Conservation AgentsDiphosphonatesBisphosphonateDrug holidaysFragility fractureHigh risk of fracture

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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.