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This version published online on January 23, 2007
Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2006-1526
A more recent version of this article appeared on April 1, 2007
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Submitted on July 13, 2006
Accepted on January 17, 2007

EFFECT OF MONITORING BONE TURNOVER MARKERS ON PERSISTENCE WITH RISEDRONATE TREATMENT OF POSTMENOPAUSAL OSTEOPOROSIS

Pierre D. Delmas MD, PhD*, Bernard Vrijens PhD, Richard Eastell MD, Christian Roux MD, Huibert A. P. Pols MD, Johann D. Ringe MD, Andreas Grauer MD, David Cahall PhD, Nelson B. Watts MD, and on behalf of IMPACT investigators

INSERM Research Unit 403 and University Claude Bernard Lyon 1, Lyon, France; AARDEX Ltd, Zug, Switzerland; University of Sheffield, Sheffield, UK; University René-Descartes, Paris, France;Erasmus University, Rotterdam, The Netherlands; Klinikum Leverkusen, Leverkusen, Germany; Procter & Gamble Pharmaceuticals, Mason, OH, USA; sanofi-aventis, Bridgewater, NJ, USA; University of Cincinnati, Cincinnati, OH, USA

* To whom correspondence should be addressed. E-mail: delmas{at}lyon.inserm.fr.

Context: Persistence with osteoporosis treatment is poor but is important for maximum benefit.

Objective: To assess the impact of physician reinforcement using bone turnover markers (BTMs) on persistence with risedronate treatment.

Design and Setting: 1-year multinational prospective, open-label, blinded study in 171 osteoporosis centers in 21 countries.

Patients: 2382 postmenopausal women (65-80 years) with spine/hip T-score ≤ -2.5 or T-score ≤ -1.0 with a low-trauma fracture.

Intervention: Calcium 500 mg/d, vitamin D 400 IU/d, and risedronate 5 mg/d for 1 year. Centers were randomized to reinforcement (RE+) or no reinforcement (RE-). At 13 and 25 weeks, reinforcement based on urinary N-telopeptide of type I collagen [uNTX] change from baseline was provided to the RE+ patients using the following response categories: good (>30% decrease), stable (-30% to +30% change) or poor (>30% increase).

Main Outcome Measures: Persistence assessed with electronic drug monitors.

Results: In the overall efficacy population (n = 2302), persistence was unexpectedly high and was similar for both groups (RE-, 77%; RE+, 80%; P = 0.160). A significant relationship between the type of message and persistence was observed (P = 0.017). Compared with RE-, intervention based on a good BTM response was associated with a significant improvement in persistence (HR=0.71; 95% CI, 0.53-0.95). Persistence was unchanged (HR=1.02; 95% CI, 0.74-1.40) or lower (HR=2.22; 95% CI, 1.27-3.89) when reinforcement was based on a stable or poor BTM response, respectively. Reinforcement was associated with a lower incidence of new radiologically determined vertebral fractures (OR=0.4; 95% CI, 0.2-1.0).

Conclusions: Reinforcement using BTMs influences persistence with treatment in postmenopausal women with osteoporosis, depending on the BTM response observed.


Key words: persistence • risedronate • multinational • bone turnover • reinforcement




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