Osteoporosis, bone & mineral

Effects of romosozumab on the peripheral and axial skeleton in postmenopausal women at high fracture risk: real-world evidence from DXA and high-resolution peripheral quantitative CT (HR-pQCT) data

Osteoporos IntPublished Retrospective cohort study

Authors' conclusion

After 12 months of ROMO treatment, aBMD increased significantly at the lumbar spine and total hip, while volumetric BMD, microarchitecture, and strength at the peripheral skeleton did not change or deteriorated.

Study context

Population
Postmenopausal women at high fracture risk, regular hospital care
Participants
28 vs 55
Exposure
Romosozumab vs bisphosphonate treatment
  • ROMOn = 28
  • Bisphosphonate (BP)n = 55reference
Outcome
Change in aBMD (DXA) and HR-pQCT parameters with ROMO, T0 to T1
Follow-up
12 months
Methodological detailsreal-world data, single-centre, age-matched comparison cohort
  • Real-world data
  • Single-centre
  • Age-matched comparison cohort

Main finding

As reported in the abstract

12 months
Lumbar spine areal bone mineral density (aBMD) change: +9.6% [IQR = 6.6,15.7]
p < 0.001
Total hip aBMD change: +4.4 ± 5.8%
p = 0.001
Distal radius total volumetric BMD change: −2.4%, [−4.3,−0.1]
p = 0.004
Distal radius trabecular volumetric BMD change: −1.7%, [−3.5,0.5]
p = 0.013

Observational data: associations, not effects.

Further findings

HR-pQCT changes, ROMO vs BP cohort · 12 months

Most HR-pQCT changes did not significantly differ from those in the BP cohort

Baseline (T0) aBMD T-scores, ROMO

Lumbar spine T-score
−2.3 ± 1.6
Total hip T-score
−2.1 ± 0.7
Femoral neck T-score
−2.7 ± 0.5
  • ROMO: 72.4 ± 7.6 years, 67.9% treatment-naïve

Original publication

Effects of romosozumab on the peripheral and axial skeleton in postmenopausal women at high fracture risk: real-world evidence from DXA and HR-pQCT data. Osteoporos Int. Published 9 September 2026. doi:10.1007/s00198-026-08148-6

Composed by AI from the published abstract and checked against it. How Briefs are made →

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