Long term effects on biochemical bone markers of a single infusion of zoledronic acid in Paget disease of bone

2020 ◽  
Vol 25 (4) ◽  
pp. 715-718
Author(s):  
Celia Rodríguez-Olleros Rodríguez ◽  
Daniel Blanes Jacquart ◽  
Rosa Arboiro Pinel ◽  
Concha de la Piedra Gordo ◽  
María Jesús Moro Álvarez ◽  
...  
2000 ◽  
Vol 46 (5) ◽  
pp. 684-690 ◽  
Author(s):  
Henning W Woitge ◽  
Heike Oberwittler ◽  
Silke Heichel ◽  
Andreas Grauer ◽  
Reinhard Ziegler ◽  
...  

Abstract 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.


2013 ◽  
Vol 94 (3) ◽  
pp. 311-318 ◽  
Author(s):  
Jean-Pierre Devogelaer ◽  
Piet Geusens ◽  
Evis Daci ◽  
Evelien Gielen ◽  
Kris Denhaerynck ◽  
...  

2014 ◽  
Vol 25 (9) ◽  
pp. 2221-2223 ◽  
Author(s):  
E. K. Baykan ◽  
L. F. Saygılı ◽  
M. Erdogan ◽  
S. Cetinkalp ◽  
A. G. Ozgen ◽  
...  

2013 ◽  
Vol 93 (3) ◽  
pp. 249-252 ◽  
Author(s):  
Maurizio Rossini ◽  
Silvano Adami ◽  
Ombretta Viapiana ◽  
Gaia Tripi ◽  
Roberta Zanotti ◽  
...  

2014 ◽  
Author(s):  
Emine Kartal Baykan ◽  
L Fusun Saygili ◽  
Mehmet Erdogan ◽  
A Gokhan Ozgen ◽  
Sevki Cetinkalp ◽  
...  

2019 ◽  
Vol 8 (6) ◽  
pp. 784 ◽  
Author(s):  
Rafael Delgado-Ruiz ◽  
Patricia Swanson ◽  
Georgios Romanos

This study seeks to evaluate the long-term effects of pharmacologic therapy on the bone markers and bone mineral density of transgender patients and to provide a basis for understanding its potential implications on therapies involving implant procedures. Following the referred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and well-defined PICOT (Problem/Patient/Population, Intervention, Comparison, Outcome, Time) questionnaires, a literature search was completed for articles in English language, with more than a 3 year follow-up reporting the long-term effects of the cross-sex pharmacotherapy on the bones of adult transgender patients. Transgender demographics, time under treatment, and treatment received were recorded. In addition, bone marker levels (calcium, phosphate, alkaline phosphatase, and osteocalcin), bone mineral density (BMD), and bone turnover markers (Serum Procollagen type I N-Terminal pro-peptide (PINP), and Serum Collagen type I crosslinked C-telopeptide (CTX)) before and after the treatment were also recorded. The considerable variability between studies did not allow a meta-analysis. All the studies were completed in European countries. Transwomen (921 men to female) were more frequent than transmen (719 female to male). Transwomen’s treatments were based in antiandrogens, estrogens, new drugs, and sex reassignment surgery, meanwhile transmen’s surgeries were based in the administration of several forms of testosterone and sex reassignment. Calcium, phosphate, alkaline phosphatase, and osteocalcin levels remained stable. PINP increased in transwomen and transmen meanwhile, CTX showed contradictory values in transwomen and transmen. Finally, reduced BMD was observed in transwomen patients receiving long-term cross-sex pharmacotherapy. Considering the limitations of this systematic review, it was concluded that long-term cross-sex pharmacotherapy for transwomen and transmen transgender patients does not alter the calcium, phosphate, alkaline phosphatase, and osteocalcin levels, and will slightly increase the bone formation in both transwomen and transmen patients. Furthermore, long-term pharmacotherapy reduces the BMD in transwomen patients.


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