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The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis
OBJECTIVE: To investigate the efficacy of minodronate in the treatment of glucocorticoid-induced osteoporosis (GIO). METHODS: The study population included patients in whom the administration of minodronate (50 mg, once every 4 weeks) had been newly started for the treatment of GIO in Niigata Rheuma...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120818/ https://www.ncbi.nlm.nih.gov/pubmed/29607978 http://dx.doi.org/10.2169/internalmedicine.9885-17 |
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author | Hasegawa, Eriko Ito, Satoshi Takai, Chinatsu Kobayashi, Daisuke Nomura, Yumi Otani, Hiroshi Abe, Asami Ishikawa, Hajime Murasawa, Akira Narita, Ichiei Nakazono, Kiyoshi |
author_facet | Hasegawa, Eriko Ito, Satoshi Takai, Chinatsu Kobayashi, Daisuke Nomura, Yumi Otani, Hiroshi Abe, Asami Ishikawa, Hajime Murasawa, Akira Narita, Ichiei Nakazono, Kiyoshi |
author_sort | Hasegawa, Eriko |
collection | PubMed |
description | OBJECTIVE: To investigate the efficacy of minodronate in the treatment of glucocorticoid-induced osteoporosis (GIO). METHODS: The study population included patients in whom the administration of minodronate (50 mg, once every 4 weeks) had been newly started for the treatment of GIO in Niigata Rheumatic Center from 2012 to 2015. Patients who were bisphosphonate-naïve and those who switched from other bisphosphonates were classified into the naïve and switch groups, respectively. The changes in the bone mineral density (BMD) and bone metabolic markers after one year of minodronate treatment were retrospectively evaluated. We also compared the BMD and bone turnover marker changes of minodronate-naïve patients with those in whom alendronate or risedronate had been prescribed as a first bisphosphonate (control group). RESULTS: Minodronate was prescribed to 142 patients, and data were successfully obtained from 120 patients. New vertebral fractures were observed in 5 of the 142 patients; 1 fracture occurred during the cessation of minodronate for dental treatment, and 3 patients already had multiple vertebral fractures before the initiation of minodronate. The patients' tartrate-resistant acid phosphatase 5b (TRACP-5b) (-27.0%, p<0.001) and bone alkaline phosphatase (BAP) (-15.7%, p<0.01) levels were decreased, but no patients showed a decrease to below the normal range. One year of treatment with minodronate significantly increased the lumbar BMD in the naïve (+3.9%, p<0.001) and switch (+2.3%, p<0.001) groups. Although the femoral BMD did not change to a significant extent overall, the patients with a low young adult mean (YAM) (<80%) at baseline showed a significant increase in their femoral BMD (+2.1%, p=0.034) values. Compared with the control group, the minodronate-naïve group showed a significant decrease in the TRACP-5b levels and a significant increase in the lumbar BMD. CONCLUSION: The administration of minodronate appears to be an effective treatment for GIO. |
format | Online Article Text |
id | pubmed-6120818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-61208182018-09-04 The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis Hasegawa, Eriko Ito, Satoshi Takai, Chinatsu Kobayashi, Daisuke Nomura, Yumi Otani, Hiroshi Abe, Asami Ishikawa, Hajime Murasawa, Akira Narita, Ichiei Nakazono, Kiyoshi Intern Med Original Article OBJECTIVE: To investigate the efficacy of minodronate in the treatment of glucocorticoid-induced osteoporosis (GIO). METHODS: The study population included patients in whom the administration of minodronate (50 mg, once every 4 weeks) had been newly started for the treatment of GIO in Niigata Rheumatic Center from 2012 to 2015. Patients who were bisphosphonate-naïve and those who switched from other bisphosphonates were classified into the naïve and switch groups, respectively. The changes in the bone mineral density (BMD) and bone metabolic markers after one year of minodronate treatment were retrospectively evaluated. We also compared the BMD and bone turnover marker changes of minodronate-naïve patients with those in whom alendronate or risedronate had been prescribed as a first bisphosphonate (control group). RESULTS: Minodronate was prescribed to 142 patients, and data were successfully obtained from 120 patients. New vertebral fractures were observed in 5 of the 142 patients; 1 fracture occurred during the cessation of minodronate for dental treatment, and 3 patients already had multiple vertebral fractures before the initiation of minodronate. The patients' tartrate-resistant acid phosphatase 5b (TRACP-5b) (-27.0%, p<0.001) and bone alkaline phosphatase (BAP) (-15.7%, p<0.01) levels were decreased, but no patients showed a decrease to below the normal range. One year of treatment with minodronate significantly increased the lumbar BMD in the naïve (+3.9%, p<0.001) and switch (+2.3%, p<0.001) groups. Although the femoral BMD did not change to a significant extent overall, the patients with a low young adult mean (YAM) (<80%) at baseline showed a significant increase in their femoral BMD (+2.1%, p=0.034) values. Compared with the control group, the minodronate-naïve group showed a significant decrease in the TRACP-5b levels and a significant increase in the lumbar BMD. CONCLUSION: The administration of minodronate appears to be an effective treatment for GIO. The Japanese Society of Internal Medicine 2018-03-30 2018-08-01 /pmc/articles/PMC6120818/ /pubmed/29607978 http://dx.doi.org/10.2169/internalmedicine.9885-17 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Hasegawa, Eriko Ito, Satoshi Takai, Chinatsu Kobayashi, Daisuke Nomura, Yumi Otani, Hiroshi Abe, Asami Ishikawa, Hajime Murasawa, Akira Narita, Ichiei Nakazono, Kiyoshi The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title | The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title_full | The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title_fullStr | The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title_full_unstemmed | The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title_short | The Efficacy of Minodronate in the Treatment of Glucocorticoid-induced Osteoporosis |
title_sort | efficacy of minodronate in the treatment of glucocorticoid-induced osteoporosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120818/ https://www.ncbi.nlm.nih.gov/pubmed/29607978 http://dx.doi.org/10.2169/internalmedicine.9885-17 |
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