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Clinical Chemistry 46: 684-690, 2000;
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(Clinical Chemistry. 2000;46:684-690.)
© 2000 American Association for Clinical Chemistry, Inc.


Articles

Short- and Long-Term Effects of Ibandronate Treatment on Bone Turnover in Paget Disease of Bone

Henning W. Woitge, Heike Oberwittler, Silke Heichel, Andreas Grauer, Reinhard Ziegler and Markus J. Seibela

Department of Internal Medicine, Division of Endocrinology and Metabolism, University of Heidelberg, Bergheimerstrasse 58, D-69115 Heidelberg, Germany.
a Author for correspondence. Fax 49-6221-564101; e-mail Markus_Seibel{at}med.uni-heidelberg.de

Background: In Paget disease of bone (PD), serum total alkaline phosphatase (TAP) is a valid marker of disease activity. The aim of the present longitudinal study was to compare TAP with new and potentially more specific markers of bone turnover in bisphosphonate-treated patients with PD.

Methods: Twenty patients with active PD were studied before and after treatment with 2 mg of intravenous ibandronate over a period of 12 months. TAP (by colorimetry), serum bone-specific alkaline phosphatase (BAP; by enzyme immunoassay), serum osteocalcin (OC; by ELISA), serum bone sialoprotein (BSP; by RIA), and urinary total pyridinoline (PYD; by HPLC) and deoxypyridinoline (DPD; by HPLC) were measured as markers of bone turnover.

Results: Before treatment, TAP, BAP, and BSP were increased in all 20 patients, whereas OC was increased in 10, PYD in 13, and DPD in 15 patients. Three months post treatment, nine patients showed normalized TAP values, and a >=25% re-increase (i.e., relapse) was observed in all patients after 12 months. A normalization of BAP was achieved in six patients only. No significant changes were found for OC. BSP was decreased significantly at 24 h, and DPD at 48 h post treatment. A normalization of BSP was found in 8, of PYD in 18, and of DPD in 16 cases. Both PYD and DPD increased significantly from 9 months post treatment onward.

Conclusions: Most markers of bone turnover show similar long-term changes after treatment of active PD with ibandronate. With regard to cost-effectiveness and assay performance, TAP remains the marker of choice in therapeutic monitoring of PD. However, more specific markers may improve the biochemical assessment of PD in certain situations.




The following articles in journals at HighWire Press have cited this article:


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Clin. Chem.Home page
M. E. Kraenzlin, C. A. Kraenzlin, C. Meier, C. Giunta, and B. Steinmann
Automated HPLC Assay for Urinary Collagen Cross-links: Effect of Age, Menopause, and Metabolic Bone Diseases
Clin. Chem., September 1, 2008; 54(9): 1546 - 1553.
[Abstract] [Full Text] [PDF]


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J Clin PharmacolHome page
J. Barrett, E. Worth, F. Bauss, and S. Epstein
Ibandronate: A Clinical Pharmacological and Pharmacokinetic Update
J. Clin. Pharmacol., September 1, 2004; 44(9): 951 - 965.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
H. W. Woitge, E. Horn, A. V. Keck, B. Auler, M. J. Seibel, and M. Pecherstorfer
Biochemical Markers of Bone Formation in Patients with Plasma Cell Dyscrasias and Benign Osteoporosis
Clin. Chem., April 1, 2001; 47(4): 686 - 693.
[Abstract] [Full Text] [PDF]




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