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  3. Long-term impact of teriparatide on bone mineral density, trabecular bone score, and fracture risk relative to total hip T-score: A two-decade, registry-based cohort study.
 

Long-term impact of teriparatide on bone mineral density, trabecular bone score, and fracture risk relative to total hip T-score: A two-decade, registry-based cohort study.

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BORIS DOI
10.48620/86532
Date of Publication
March 5, 2025
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Clinic of Rheumatolog...

Institute of Anatomy

University Clinic for...

Contributor
Guyer, Laura
Lehmann, Oliver
Wenger, Mathias
Oser, Sven
Studer, Ueli
Steiner, Christian
Ziswiler, Hans-Rudolf
Schmid, Gernot
Häuselmann, HansJörg
Reichenbach, Stephan
Institut für Sozial- und Präventivmedizin (ISPM) - Musculoskeletal Health & Rheumatology
Clinic of Rheumatology and Immunology
Lehmann, Thomas
Everts-Graber, Judith
Clinic of Rheumatology and Immunology
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
Bone
ISSN or ISBN (if monograph)
1873-2763
8756-3282
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.bone.2025.117445
PubMed ID
40054513
Uncontrolled Keywords

Bone Mineral Density

Fractures

Osteoanabolic

Osteoporosis

Teriparatide

Description
Background
Teriparatide followed by antiresorptive therapy exhibits fracture reduction efficacy for up to 2 years, but it remains unclear if this leads to sustained increases in bone mineral density (BMD) and trabecular bone score (TBS), and if BMD correlates with fracture risk reduction.
Methods
In this multicenter cohort study, the effect of teriparatide administration for 18-24 months, followed by antiresorptive therapy, was assessed in patients partipicipating in a nationwide Swiss osteoporosis registry. BMD and TBS were measured up to 10 years before and after teriparatide initiation.
Results
A total of 624 patients (87 % female, age 67 ± 13 years) were enrolled from May 2004 to December 2023. Among them, 198 (32 %) received no treatment prior to teriparatide, while 426 had received previous antiresorptive therapies (median duration 5.9 years [2.2, 8.0]). All patients underwent subsequent antiresorptive therapy, mainly with bisphosphonates and denosumab. The incidences of vertebral, hip, and any fractures were 0.96, 0.11, and 1.37, respectively, within 2 years prior to teriparatide initiation. The total hip T-score did not correlate with fracture reduction under teriparatide. After transitioning from teriparatide to an antiresorptive regimen, fracture incidence remained low and BMD was significantly higher for up to 5 years after teriparatide compared to the pre-treatment period (T-score + 0.876 for lumbar spine, p < 0.001; and + 0.112 for total hip, p < 0.005), while TBS increased by 0.047 (p < 0.001). Overall, significant improvement was observed in pretreated and treatment-naïve patients undergoing teriparatide treatment.
Conclusion
Teriparatide led to sustained lower incidences of vertebral, hip, and other fractures for up to 8 years after switching to antiresorptive agents in both pretreated and treatment-naïve patients. Additionally, BMD and TBS levels were significantly higher than those before teriparatide treatment. During teriparatide treatment, the total hip T-score did not correlate with fracture risk.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/206540
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S8756328225000572-main.pdftextAdobe PDF3.21 MBpublishedOpen
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