Evidence map›Paper›PMID 41991651›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2026

Vertebral fractures and muscle function in glucocorticoid-treated individuals with Duchenne muscular dystrophy: a cohort study.

Anna Capasso, Chiara Arpaia, Chiara Panicucci, Consolato Gulli, Marianna Villa, Agnese Repetto, Giorgia Coratti, Simone Morando, Gianpaolo Cicala, Alessandro Oliva and 14 more

Abstract read
In one paragraph

Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

24 authors.

Anna Capasso *Pediatric Neurology Unit, Catholic University, Rome, Italy.
Chiara Arpaia *Pediatric Neurology Unit, Catholic University, Rome, Italy.
Chiara PanicucciCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Consolato GulliAdvanced Radiology Center, Department of Diagnostic Imaging and Radiation Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Marianna VillaCentro Clinico Nemo, U.O.C. Neuropsichiatria Infantile Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Agnese RepettoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Giorgia CorattiPediatric Neurology Unit, Catholic University, Rome, Italy.
Simone MorandoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Gianpaolo CicalaPediatric Neurology Unit, Catholic University, Rome, Italy.
Alessandro OlivaComplex Operative Unit of Internal Medicine, Endocrinology and Diabetology, Department of Translational Medicine and Surgery, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
Domenico MilardiComplex Operative Unit of Internal Medicine, Endocrinology and Diabetology, Department of Translational Medicine and Surgery, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
Clelia CipollaPediatric Unit, Department of Life Sciences and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Gennaro CatapanoPediatric Neurology Unit, Catholic University, Rome, Italy.
Anna MarzoliRadiology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maria Beatrice DamasioRadiology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Claudia BrognaPediatric Neurology Unit, Catholic University, Rome, Italy.
Concetta PalermoCentro Clinico Nemo, U.O.C. Neuropsichiatria Infantile Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Natascia Di IorgiDepartment of Pediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Claudio BrunoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Luana FicocielloAdvanced Radiology Center, Department of Diagnostic Imaging and Radiation Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Simona GaudinoAdvanced Radiology Center, Department of Diagnostic Imaging and Radiation Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Marika PanePediatric Neurology Unit, Catholic University, Rome, Italy.
Leanne M WardDivision of Endocrinology and Metabolism, Children's Hospital of Eastern Ontario and University of Ottawa, Ottawa, ON, Canada.
Eugenio MercuriPediatric Neurology Unit, Catholic University, Rome, Italy. eugeniomaria.mercuri@unicatt.it.ORCID http://orcid.org/0000-0002-9851-5365

Funding

Fondazione Telethon GUP23005
6 · The paper itself

Abstract

Brief rationale: To investigate vertebral fracture and risk factors in DMD. MAIN

resultsVertebral fractures were found in 42% of subjects with an increased risk associated with low TB BMD, early steroid exposure and low BMI. Significance of the paper: Bone health monitoring should start early, regardless of functional status. PURPOSE: To describe the prevalence of vertebral fractures (VFs) in Duchenne Muscular Dystrophy (DMD) and to establish the role of several risk factors, focusing on ambulatory status and functional motor scores (Performance Upper Limb, North Star Ambulatory Assessment) not previously assessed.

methodsWe recorded the number and site of fractures together with anthropometric, radiological (total body bone mineral density (TB BMD) Z-scores measured by Dual Energy X-ray Absorptiometry (DXA)), and functional scales. Logistic and linear regression analyses were conducted to identify factors associated with prevalent VFs and predictors of Spinal Deformity Index (SDI).

resultsOf the 149 individuals (7-26 years) studied, 62 (42%) had VFs. These were equally present in ambulant and non-ambulant individuals (41 vs 42%) and were not associated with functional scores. The TB BMD Z-score was a protective factor both in non-ambulant and ambulant subgroups. Lower TB BMD Z-scores were also predictive of a greater SDI. In the ambulant subgroup a lower BMI reduced the risk of VF. In the overall cohort, each one-year delay in starting glucocorticoids reduced the risk of VFs by 27% (p = 0.007), and each additional unit in TB BMD Z-score reduced the risk of VFs by 54% (p = 0.0007).

conclusionOur results suggest that ambulatory status and functional scores alone may not be reliable predictors for developing VFs and confirm the association with known risk factors, such as early initiation of glucocorticoid therapy and low BMD Z-scores, highlighting the need to guarantee a careful surveillance of possible VFs from the time of glucocorticoid initiation.

Indexed as

GlucocorticoidsMuscular Dystrophy, DuchenneOsteoporotic FracturesSpinal FracturesAbsorptiometry, PhotonAdolescentAdultAnthropometryBody Mass IndexBone DensityChildCohort StudiesHumansMaleMuscle, SkeletalRisk FactorsGlucocorticoidsBone fragilityDMDFracturesFunctional status

Identifiers

PMID41991651
PMCPMC13553609

What OpenQuestion holds

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Registered trials

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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.