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Efficacy of Oral Etidronate for Skeletal Diseases in Japan

Etidronate is an oral bisphosphonate compound that is known to reduce bone resorption through the inhibition of osteoclastic activity. The efficacy of etidronate for involutional (postmenopausal and senile) and glucocorticoid-induced osteoporosis, as well as that for other skeletal diseases, was rev...

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Autores principales: Iwamoto, Jun, Takeda, Tsuyoshi, Sato, Yoshihiro
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815806/
https://www.ncbi.nlm.nih.gov/pubmed/15988801
http://dx.doi.org/10.3349/ymj.2005.46.3.313
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author Iwamoto, Jun
Takeda, Tsuyoshi
Sato, Yoshihiro
author_facet Iwamoto, Jun
Takeda, Tsuyoshi
Sato, Yoshihiro
author_sort Iwamoto, Jun
collection PubMed
description Etidronate is an oral bisphosphonate compound that is known to reduce bone resorption through the inhibition of osteoclastic activity. The efficacy of etidronate for involutional (postmenopausal and senile) and glucocorticoid-induced osteoporosis, as well as that for other skeletal diseases, was reviewed in Japanese patients. Cyclical etidronate treatment (200 mg or 400 mg/day for 2 weeks about every 3 months) increases the lumbar bone mineral density (BMD) in patients with involutional osteoporosis and prevents incident vertebral fractures in patients with glucocorticoid-induced osteoporosis. The losses of the lumbar BMD in patients with liver cirrhosis and the metacarpal BMD in hemiplegic patients after stroke are prevented, and the lumbar BMD is possibly increased, preventing fragile fractures in adult patients with osteogenesis imperfecta type I. Furthermore, proximal bone resorption around the femoral stem is reduced and some complications may be prevented in patients who undergo cementless total hip arthroplasty. Oral etidronate treatment may also help to transiently relieve metastatic cancer bone pain followed by a decrease in abnormally raised bone resorption in patients with painful bone metastases from primary cancer sites, such as the lung, breast and prostate. Thus, oral etidronate treatment is suggested to be efficacious for osteoporosis, as well as other skeletal diseases associated with increased bone resorption, in Japanese patients. Randomized controlled trials needed to be conducted on a large number of patients to confirm these effects.
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spelling pubmed-28158062010-02-04 Efficacy of Oral Etidronate for Skeletal Diseases in Japan Iwamoto, Jun Takeda, Tsuyoshi Sato, Yoshihiro Yonsei Med J Review Article Etidronate is an oral bisphosphonate compound that is known to reduce bone resorption through the inhibition of osteoclastic activity. The efficacy of etidronate for involutional (postmenopausal and senile) and glucocorticoid-induced osteoporosis, as well as that for other skeletal diseases, was reviewed in Japanese patients. Cyclical etidronate treatment (200 mg or 400 mg/day for 2 weeks about every 3 months) increases the lumbar bone mineral density (BMD) in patients with involutional osteoporosis and prevents incident vertebral fractures in patients with glucocorticoid-induced osteoporosis. The losses of the lumbar BMD in patients with liver cirrhosis and the metacarpal BMD in hemiplegic patients after stroke are prevented, and the lumbar BMD is possibly increased, preventing fragile fractures in adult patients with osteogenesis imperfecta type I. Furthermore, proximal bone resorption around the femoral stem is reduced and some complications may be prevented in patients who undergo cementless total hip arthroplasty. Oral etidronate treatment may also help to transiently relieve metastatic cancer bone pain followed by a decrease in abnormally raised bone resorption in patients with painful bone metastases from primary cancer sites, such as the lung, breast and prostate. Thus, oral etidronate treatment is suggested to be efficacious for osteoporosis, as well as other skeletal diseases associated with increased bone resorption, in Japanese patients. Randomized controlled trials needed to be conducted on a large number of patients to confirm these effects. Yonsei University College of Medicine 2005-06-30 2005-06-30 /pmc/articles/PMC2815806/ /pubmed/15988801 http://dx.doi.org/10.3349/ymj.2005.46.3.313 Text en Copyright © 2005 The Yonsei University College of Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Iwamoto, Jun
Takeda, Tsuyoshi
Sato, Yoshihiro
Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title_full Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title_fullStr Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title_full_unstemmed Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title_short Efficacy of Oral Etidronate for Skeletal Diseases in Japan
title_sort efficacy of oral etidronate for skeletal diseases in japan
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2815806/
https://www.ncbi.nlm.nih.gov/pubmed/15988801
http://dx.doi.org/10.3349/ymj.2005.46.3.313
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