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dc.contributor.author Geusens, P
dc.contributor.author Marin, F
dc.contributor.author Kendler, DL
dc.contributor.author Russo, LA
dc.contributor.author Zerbini, CA
dc.contributor.author Minisola, S
dc.contributor.author Body, JJ
dc.contributor.author Lespessailles, E
dc.contributor.author Greenspan, SL
dc.contributor.author Bagur, A
dc.contributor.author Stepan, JJ
dc.contributor.author Lakatos, Péter
dc.contributor.author Casado, E
dc.contributor.author Moericke, R
dc.contributor.author Lopez-Romero, P
dc.contributor.author Fahrleitner-Pammer, A
dc.date.accessioned 2020-03-18T09:27:24Z
dc.date.available 2020-03-18T09:27:24Z
dc.date.issued 2018
dc.identifier.citation journalVolume=33;journalIssueNumber=5;journalTitle=JOURNAL OF BONE AND MINERAL RESEARCH;pagerange=783-794;journalAbbreviatedTitle=J BONE MINER RES;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/7199
dc.identifier.uri doi:10.1002/jbmr.3384
dc.description.abstract The 2-year, randomized, double-blind, active-controlled fracture endpoint VERO study included postmenopausal women with established osteoporosis, who had at least 2 moderate or 1 severe baseline vertebral fractures (VFx), and bone mineral density (BMD) T-score </=-1.5. Patients were treated with either s.c. daily teriparatide 20 mug or oral weekly risedronate 35 mg. As previously reported, the risk of new VFx and clinical fractures (a composite of clinical VFx and nonvertebral fragility fractures [NVFFx]) was statistically significantly reduced with teriparatide compared with risedronate. Here we present the prospectively planned subgroup analyses of fracture data across subgroups, which were predefined by the following baseline characteristics: age, number and severity of prevalent VFx, prevalent nonvertebral fractures (NVFx), glucocorticoid use, prior osteoporosis drugs, recent bisphosphonate use, clinical VFx in the year before study entry, and baseline BMD. Heterogeneity of the treatment effect on the primary endpoint (new VFx), and the four key secondary endpoints (including clinical fractures and NVFFx) were investigated by logistic and Cox proportional hazards regression models. A total of 1360 women were randomized and treated (680 per group). Mean age was 72.1 years, mean (SD) number of prevalent VFx was 2.7 (2.1), 55.4% had a BMD T-score <-2.5, 36.5% had a recent clinical VFx, 28.3% had a prior major NVFx, 43.2% were osteoporosis drug-naive, 39.3% were recent bisphosphonate users, and 9.3% were taking glucocorticoids at a prednisone-equivalent dose of >5 mg/d. For most fracture endpoints, the risk reduction of teriparatide versus risedronate did not significantly differ in any of the subgroups analyzed (treatment-by-subgroup interaction p > 0.1), with most subgroups mirroring results from the total study population. In conclusion, in postmenopausal women with severe osteoporosis, the antifracture efficacy of teriparatide compared with risedronate was consistent in a wide range of patient settings, including treatment-naive and previously treated patients. (c) 2018 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals Inc.
dc.format.extent 783-794
dc.relation.ispartof urn:issn:0884-0431
dc.title Effects of Teriparatide Compared with Risedronate on the Risk of Fractures in Subgroups of Postmenopausal Women with Severe Osteoporosis: The VERO Trial
dc.type Journal Article
dc.date.updated 2019-07-08T13:14:59Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 3358512
dc.identifier.wos 000432006800004
dc.identifier.pubmed 29329484
dc.contributor.department SE/AOK/K/I. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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