ReviewCureus2025
Denosumab Versus Bisphosphonates in Glucocorticoid-Induced Osteoporosis: A Systematic Review.
Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Glucocorticoid-induced osteoporosis (GIOP) is a major cause of secondary bone loss characterized by rapid trabecular deterioration and increased fracture risk, and while bisphosphonates are widely used as first-line therapy, the comparative effectiveness of denosumab remains clinically relevant. This systematic review synthesized evidence from randomized trials, imaging studies, and observational cohorts evaluating denosumab versus bisphosphonates in adults receiving glucocorticoids, focusing on bone mineral density, bone turnover, microarchitecture, fractures, and safety. Denosumab consistently produced greater increases in lumbar spine bone mineral density, with modest but generally favorable effects at the hip and variable advantages at the femoral neck. High-resolution imaging suggested superior preservation of cortical thickness, trabecular density, and estimated bone strength with denosumab, accompanied by deeper suppression of bone turnover markers across studies. Fracture outcomes did not demonstrate meaningful differences between treatments, likely due to limited power and relatively short follow-up. Safety profiles were broadly comparable, without significant variation in adverse events or serious complications. Overall, denosumab appears to offer stronger densitometric and mechanistic benefits than bisphosphonates in GIOP, supporting its use in patients who are inadequately responsive to alternative therapies or require long-term glucocorticoid treatment, although larger and longer trials with fracture endpoints are still needed.
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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.