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New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide

Daily 20-μg and once-weekly 56.5-μg teriparatide (parathyroid hormone 1–34) treatment regimens increase bone mineral density (BMD) and prevent fractures, but changes in bone turnover markers differ between the two regimens. The aim of the present study was to explain changes in bone turnover markers...

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Autores principales: Tanaka, Sakae, Adachi, Taiji, Kuroda, Tatsuhiko, Nakamura, Toshitaka, Shiraki, Masataka, Sugimoto, Toshitsugu, Takeuchi, Yasuhiro, Saito, Mitsuru, Bilezikian, John P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472137/
https://www.ncbi.nlm.nih.gov/pubmed/26273530
http://dx.doi.org/10.1038/boneres.2014.43
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author Tanaka, Sakae
Adachi, Taiji
Kuroda, Tatsuhiko
Nakamura, Toshitaka
Shiraki, Masataka
Sugimoto, Toshitsugu
Takeuchi, Yasuhiro
Saito, Mitsuru
Bilezikian, John P
author_facet Tanaka, Sakae
Adachi, Taiji
Kuroda, Tatsuhiko
Nakamura, Toshitaka
Shiraki, Masataka
Sugimoto, Toshitsugu
Takeuchi, Yasuhiro
Saito, Mitsuru
Bilezikian, John P
author_sort Tanaka, Sakae
collection PubMed
description Daily 20-μg and once-weekly 56.5-μg teriparatide (parathyroid hormone 1–34) treatment regimens increase bone mineral density (BMD) and prevent fractures, but changes in bone turnover markers differ between the two regimens. The aim of the present study was to explain changes in bone turnover markers using once-weekly teriparatide with a simulation model. Temporary increases in bone formation markers and subsequent decreases were observed during once-weekly teriparatide treatment for 72 weeks. These observations support the hypothesis that repeated weekly teriparatide administration stimulates bone remodeling, replacing old bone with new bone and leading to a reduction in the active remodeling surface. A simulation model was developed based on the iterative remodeling cycle that occurs on residual old bone. An increase in bone formation and a subsequent decrease were observed in the preliminary simulation. For each fitted time point, the predicted value was compared to the absolute values of the bone formation and resorption markers and lumbar BMD. The simulation model strongly matched actual changes in bone turnover markers and BMD. This simulation model indicates increased bone formation marker levels in the early stage and a subsequent decrease. It is therefore concluded that remodeling-based bone formation persisted during the entire treatment period with once-weekly teriparatide.
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spelling pubmed-44721372015-08-13 New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide Tanaka, Sakae Adachi, Taiji Kuroda, Tatsuhiko Nakamura, Toshitaka Shiraki, Masataka Sugimoto, Toshitsugu Takeuchi, Yasuhiro Saito, Mitsuru Bilezikian, John P Bone Res Article Daily 20-μg and once-weekly 56.5-μg teriparatide (parathyroid hormone 1–34) treatment regimens increase bone mineral density (BMD) and prevent fractures, but changes in bone turnover markers differ between the two regimens. The aim of the present study was to explain changes in bone turnover markers using once-weekly teriparatide with a simulation model. Temporary increases in bone formation markers and subsequent decreases were observed during once-weekly teriparatide treatment for 72 weeks. These observations support the hypothesis that repeated weekly teriparatide administration stimulates bone remodeling, replacing old bone with new bone and leading to a reduction in the active remodeling surface. A simulation model was developed based on the iterative remodeling cycle that occurs on residual old bone. An increase in bone formation and a subsequent decrease were observed in the preliminary simulation. For each fitted time point, the predicted value was compared to the absolute values of the bone formation and resorption markers and lumbar BMD. The simulation model strongly matched actual changes in bone turnover markers and BMD. This simulation model indicates increased bone formation marker levels in the early stage and a subsequent decrease. It is therefore concluded that remodeling-based bone formation persisted during the entire treatment period with once-weekly teriparatide. Nature Publishing Group 2014-12-23 /pmc/articles/PMC4472137/ /pubmed/26273530 http://dx.doi.org/10.1038/boneres.2014.43 Text en Copyright © 2014 Sichuan University https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/)
spellingShingle Article
Tanaka, Sakae
Adachi, Taiji
Kuroda, Tatsuhiko
Nakamura, Toshitaka
Shiraki, Masataka
Sugimoto, Toshitsugu
Takeuchi, Yasuhiro
Saito, Mitsuru
Bilezikian, John P
New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title_full New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title_fullStr New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title_full_unstemmed New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title_short New simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
title_sort new simulation model for bone formation markers in osteoporosis patients treated with once-weekly teriparatide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472137/
https://www.ncbi.nlm.nih.gov/pubmed/26273530
http://dx.doi.org/10.1038/boneres.2014.43
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