Evidence map›Paper›PMID 41860715›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

A new age of osteoanabolic therapy? A real-world, two-centre study comparing effects of romosozumab, teriparatide, and antiresorptive therapies for osteoporosis.

India Richardson-Thornton, Sarah C Brennan, Livia Liu, Courtney Streeter, James Hill, Roderick J Clifton-Bligh, Christian M Girgis, Matti L Gild

Abstract readMulticenter StudyComparative Study
PubMed Publisher
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.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

India Richardson-ThorntonSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Sarah C BrennanDepartment of Endocrinology, Royal North Shore Hospital, St Leonards, NSW, 2065, Australia.
Livia LiuDepartment of Endocrinology, Royal North Shore Hospital, St Leonards, NSW, 2065, Australia.
Courtney StreeterSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
James HillSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Roderick J Clifton-BlighSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Christian M GirgisSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Matti L GildSydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, Australia. matti.gild@sydney.edu.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Romosozumab demonstrates strong real-world effectiveness in improving bone density, with particularly pronounced gains at the lumbar spine. Treatment-naïve patients derive the greatest benefit. Lumbar spine improvements surpass those achieved with teriparatide or anti-resorptive therapies, and longer prior exposure to anti-resorptives is associated with attenuated responses to romosozumab.

introductionOsteoporosis is a progressive disease that leads to considerable morbidity. The osteoanabolic agent romosozumab has shown efficacy in clinical trials, enhancing bone mineral density (BMD) and reducing fracture risk. However, real-world evidence, particularly in patients receiving long-term anti-resorptive therapy, remains limited. This study aimed to characterise real-world outcomes of romosozumab use in an Australian cohort, identifying predictors of optimal response following standard anti-resorptive treatment.

methodsThis retrospective cohort study identified 53 patients treated with romosozumab from the electronic medical record (eMR) at tertiary hospitals between 2021 and 23 who had completed 12 months of therapy and where baseline and follow-up DXA scans were available for analysis. Comparative data for teriparatide and anti-resorptive treatment cohorts were obtained from prior eMR datasets (n = 54 and n = 60, respectively).

resultsRomosozumab treatment led to BMD increases at the lumbar spine (LS), total hip (TH), and femoral neck (FN), with a decrease at the wrist (p < 0.05). Mean BMD gains at LS were significantly higher with romosozumab than with teriparatide (11.3 ± 8.2% vs. 5.0 ± 8.6%, p < 0.001) and anti-resorptive treatment (11.3 ± 8.2% vs. 6.6 ± 6.1%, p < 0.001). Treatment-naïve patients achieved more pronounced gains at LS (14.0 ± 6.6%); TH (5.0 ± 1.7%) compared to those with prior anti-resorptive therapy (LS 10.7 ± 8.5%, p = 0.220; TH 1.9 ± 5.8%, p = 0.009). Duration of previous anti-resorptive treatment was inversely correlated with LS BMD gains on romosozumab (r = - 0.305, p = 0.026). Linear regression showed that more vertebral fractures, longer prior anti-resorptive use, and higher baseline LS BMD each attenuated the LS BMD response to romosozumab, with romosozumab outperforming teriparatide and anti-resorptives, while teriparatide showed no significant difference from standard anti-resorptives.

conclusionRomosozumab provides real-world efficacy in BMD improvement, particularly at the LS, with significantly greater gains than those seen with teriparatide or standard therapies. Prior anti-resorptive use may attenuate romosozumab's anabolic effects, suggesting that treatment-naïve patients may benefit most from this therapy.

Indexed as

Antibodies, MonoclonalBone Density Conservation AgentsOsteoporosisTeriparatideAgedAged, 80 and overBone DensityFemaleFemur NeckHip JointHumansLumbar VertebraeMaleMiddle AgedOsteoporotic FracturesRetrospective StudiesAntibodies, MonoclonalBone Density Conservation AgentsromosozumabTeriparatideOsteoanabolicOsteoporosisRomosozumab

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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.