Evidence map›Paper›PMID 38987183›Full record

ArticleInternal medicine (Tokyo, Japan)2025

Effects of Denosumab and Bisphosphonates on Glucocorticoid-induced Osteoporosis in Patients with Neuroimmunological Disorders.

Hideo Handa, Akiyuki Uzawa, Masahiro Mori, Manato Yasuda, Yosuke Onishi, Hiroyuki Akamine, Etsuko Ogaya, Yoko Niibe, Hajime Yokota, Satoshi Kuwabara

Abstract readComparative Study
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. 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

10 authors.

Hideo HandaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Akiyuki UzawaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Masahiro MoriDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Manato YasudaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Yosuke OnishiDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Hiroyuki AkamineDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Etsuko OgayaDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.
Yoko NiibeDivision of Pharmacy, Chiba University Hospital, Japan.
Hajime YokotaDepartment of Diagnostic Radiology and Radiation Oncology, Graduate School of Medicine, Chiba University, Japan.
Satoshi KuwabaraDepartment of Neurology, Graduate School of Medicine, Chiba University, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Although patients with neuroimmunological disorders often need to be treated with glucocorticoids and are at risk of developing glucocorticoid-induced osteoporosis, no research has focused on the treatment of glucocorticoid-induced osteoporosis in such patients. Methods We compared the efficacy of denosumab and bisphosphonates in glucocorticoid-induced osteoporosis in neuroimmunological diseases. In 57 patients with neuroimmunological disorders treated with corticosteroids (34 with neuromyelitis optica spectrum disorders, 16 with myasthenia gravis, and 7 with others), we retrospectively studied the long-term effects of denosumab (n=23) and bisphosphonates (n=34) on spine and total hip bone mineral density (BMD) measured by dual energy X-ray absorptiometry. Results There were no significant differences in the age, lumbar spine BMD, or mean dose or duration of prednisolone administration at baseline between the denosumab and bisphosphonate groups. During the follow-up period of up to 6 years, the increase in the lumbar spine and total hip BMD was greater in the denosumab group than in the bisphosphonate group (p<0.01). Insufficient bone fractures were observed in 2 (9%) of the 23 patients in the denosumab group and in 2 (6%) of the 34 patients in the bisphosphonate group (not significant). Conclusion Denosumab is more effective than bisphosphonates in increasing the BMD of patients with neuroimmunological disorders receiving glucocorticoids.

Indexed as

Bone Density Conservation AgentsDenosumabDiphosphonatesGlucocorticoidsOsteoporosisAdultAgedBone DensityFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeBone Density Conservation AgentsDenosumabDiphosphonatesGlucocorticoidsbisphosphonatesdenosumabglucocorticoidneuroimmunological disordersosteoporosis

Identifiers

PMID38987183
PMCPMC11904454

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