Baseline Characteristics of the TOPaZ Study: Randomised Trial of Teriparatide and Zoledronic Acid Compared with Standard Care in Adults with Osteogenesis Imperfecta

Abstract

Introduction Osteogenesis imperfecta (OI) is a rare disorder causing multiple fractures throughout life. No treatment has been shown to reduce the risk of fractures in OI. Here, we present the baseline characteristics of participants in the Treatment of Osteogenesis Imperfecta with Parathyroid Hormone and Zoledronic Acid (TOPaZ) trial. The aim of the trial is to determine whether teriparatide and zoledronic acid are superior to standard care in reducing the risk of clinical fractures. Methods We summarised data on the baseline characteristics of TOPaZ participants, including demographics, genetic diagnosis, clinical features, bone density measurements, previous treatments, and fracture history. Results We recruited 350 adults with a clinical diagnosis of OI in 27 European referral centres between June 2017 and October 2022. Overall, 266 (76.2%) had type I OI, 55 (15.8%) had type IV, and 19 (5.4%) had type III. The type was unknown in 9 (2.6%). Blue sclera were noted in 80.8%, and 35.8% had dentinogenesis imperfecta. Bisphosphonates had been administered to 28.1% in the 2 years prior to enrolment. Pathogenic variants in COL1A1 or COL1A2 were found in 87.6%. Fractures occurring in the 2 years prior to enrolment were not associated with bone density. Conclusions The TOPaZ population represents a unique cohort with which to study the genetic epidemiology and outcome of OI in relation to bone density and biochemical markers of bone turnover. When the trial reports, it will also provide new insights into the effect of an anabolic therapy, followed by antiresorptive treatment in the management of OI.

Publication DOI: https://doi.org/10.1007/s00223-025-01440-3
Divisions: College of Health & Life Sciences > Aston Medical School
College of Health & Life Sciences
Aston University (General)
Funding Information: This project was funded by the Efficacy and Mechanism Evaluation (EME) Programme, a Medical Research Council (MRC) and National Institute of Health Research (NIHR) partnership (EME 14/200/18). The teriparatide was donated by Eli Lilly, Lilly House, Basing
Additional Information: Copyright © The Author(s) 2025. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/.
Uncontrolled Keywords: Bisphosphonate; Clinical trial; Genetic; Osteogenesis imperfecta; Teriparatide.
Publication ISSN: 1432-0827
Last Modified: 13 Nov 2025 10:19
Date Deposited: 13 Nov 2025 10:19
Full Text Link:
Related URLs: https://link.sp ... 223-025-01440-3 (Publisher URL)
PURE Output Type: Article
Published Date: 2025-11-08
Published Online Date: 2025-11-08
Accepted Date: 2025-09-30
Authors: Hald, Jannie Dahl
Weir, Christopher
Keerie, Catriona
Dewar, Lorna
MacLean, Morag
Milne, Lynsey
Keen, Richard
Walsh, Jennifer
Poole, Kenneth
Langdahl, Bente
Lindsay, John R.
Ghouri, Nazim
Hollick, Rosemary J.
Aspray, Terry
Crowley, Rachel K.
Cohen-Solal, Martine
Hassan Smith, Zaki (ORCID Profile 0000-0002-8387-3039)
Tuck, Stephen
Curtis, Elizabeth
Harvey, Nick
Eekhoff, E. Marelise W.
Feenstra, Johannes
Hampson, Geeta
Stone, Mike
Turton, Jane
Patel, Prashanth
Siddiqi, Mahood
Munro, Robin
Roy, Matthew
Paskins, Zoe
Narayanan, Deepa
Malcolm, Ellen
Javaid, Muhammad Kassim
Osborne, Patricia
Tang, Jonathan C.Y.
Lam, Wayne
Moore, David
Black, Holly A.
Duckworth, Andrew D.
Makaram, Navnit
Guo, Tianyu
Stenhouse, Gregor
Ralston, Stuart H.

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