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The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis

INTRODUCTION: Osteoporosis and sarcopenia are said to be similar disorders. However, few reports have described the effects of anti-osteoporosis drugs on muscle mass in clinical practice. METHODS: We selected 150 postmenopausal women with osteoporosis treated by minodronate (osteoporosis medication...

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Autores principales: Fujimoto, Kazuki, Inage, Kazuhide, Toyoguchi, Toru, Eguchi, Yawara, Orita, Sumihisa, Yamauchi, Kazuyo, Suzuki, Miyako, Kubota, Gou, Sainoh, Takeshi, Sato, Jun, Shiga, Yasuhiro, Abe, Koki, Kanamoto, Hirohito, Inoue, Masahiro, Kinoshita, Hideyuki, Norimoto, Masaki, Umimura, Tomotaka, Koda, Masao, Furuya, Takeo, Nakamura, Junichi, Akazawa, Tsutomu, Terakado, Atsushi, Takahashi, Kazuhisa, Ohtori, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Spine Surgery and Related Research 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698497/
https://www.ncbi.nlm.nih.gov/pubmed/31440661
http://dx.doi.org/10.22603/ssrr.2017-0016
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author Fujimoto, Kazuki
Inage, Kazuhide
Toyoguchi, Toru
Eguchi, Yawara
Orita, Sumihisa
Yamauchi, Kazuyo
Suzuki, Miyako
Kubota, Gou
Sainoh, Takeshi
Sato, Jun
Shiga, Yasuhiro
Abe, Koki
Kanamoto, Hirohito
Inoue, Masahiro
Kinoshita, Hideyuki
Norimoto, Masaki
Umimura, Tomotaka
Koda, Masao
Furuya, Takeo
Nakamura, Junichi
Akazawa, Tsutomu
Terakado, Atsushi
Takahashi, Kazuhisa
Ohtori, Seiji
author_facet Fujimoto, Kazuki
Inage, Kazuhide
Toyoguchi, Toru
Eguchi, Yawara
Orita, Sumihisa
Yamauchi, Kazuyo
Suzuki, Miyako
Kubota, Gou
Sainoh, Takeshi
Sato, Jun
Shiga, Yasuhiro
Abe, Koki
Kanamoto, Hirohito
Inoue, Masahiro
Kinoshita, Hideyuki
Norimoto, Masaki
Umimura, Tomotaka
Koda, Masao
Furuya, Takeo
Nakamura, Junichi
Akazawa, Tsutomu
Terakado, Atsushi
Takahashi, Kazuhisa
Ohtori, Seiji
author_sort Fujimoto, Kazuki
collection PubMed
description INTRODUCTION: Osteoporosis and sarcopenia are said to be similar disorders. However, few reports have described the effects of anti-osteoporosis drugs on muscle mass in clinical practice. METHODS: We selected 150 postmenopausal women with osteoporosis treated by minodronate (osteoporosis medication [OM] group) and 50 postmenopausal women without osteoporosis who did not receive treatment (no osteoporosis [NO] group). The OM group was further divided into two treatment subgroups: a combination of monthly minodronate and daily activated vitamin D vs. monthly minodronate alone. We measured lumbar spine and femoral neck bone mineral density (BMD) with dual-energy X-ray absorptiometry and muscle mass of the upper limbs, lower limbs, and trunk with bioelectrical impedance analysis at baseline and after 6 months. RESULTS: The OM and NO groups contained 130 and 37 patients, respectively (mean age: 73.9 ± 8.3 and 74.1 ± 10.0 years, respectively). In the OM group, lumbar spine BMD significantly increased after 6 months, while lower limb muscle mass significantly decreased. In the NO group, lumbar spine BMD and lower limb muscle mass did not significantly change after 6 months. In the OM group, BMD of the lumbar spine significantly increased but the lower limb muscle mass significantly decreased after 6 months relative to the NO group. In the combination therapy subgroup of the OM group muscle mass decreased significantly less than in the minodronate-alone subgroup. CONCLUSIONS: In postmenopausal women with osteoporosis, minodronate can increase BMD but cannot increase muscle mass. However, simultaneous use of activated vitamin D can suppress muscle mass decrease. The combination of activated vitamin D and minodronate may be useful for treating osteoporosis in postmenopausal women.
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spelling pubmed-66984972019-08-22 The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis Fujimoto, Kazuki Inage, Kazuhide Toyoguchi, Toru Eguchi, Yawara Orita, Sumihisa Yamauchi, Kazuyo Suzuki, Miyako Kubota, Gou Sainoh, Takeshi Sato, Jun Shiga, Yasuhiro Abe, Koki Kanamoto, Hirohito Inoue, Masahiro Kinoshita, Hideyuki Norimoto, Masaki Umimura, Tomotaka Koda, Masao Furuya, Takeo Nakamura, Junichi Akazawa, Tsutomu Terakado, Atsushi Takahashi, Kazuhisa Ohtori, Seiji Spine Surg Relat Res Original Article INTRODUCTION: Osteoporosis and sarcopenia are said to be similar disorders. However, few reports have described the effects of anti-osteoporosis drugs on muscle mass in clinical practice. METHODS: We selected 150 postmenopausal women with osteoporosis treated by minodronate (osteoporosis medication [OM] group) and 50 postmenopausal women without osteoporosis who did not receive treatment (no osteoporosis [NO] group). The OM group was further divided into two treatment subgroups: a combination of monthly minodronate and daily activated vitamin D vs. monthly minodronate alone. We measured lumbar spine and femoral neck bone mineral density (BMD) with dual-energy X-ray absorptiometry and muscle mass of the upper limbs, lower limbs, and trunk with bioelectrical impedance analysis at baseline and after 6 months. RESULTS: The OM and NO groups contained 130 and 37 patients, respectively (mean age: 73.9 ± 8.3 and 74.1 ± 10.0 years, respectively). In the OM group, lumbar spine BMD significantly increased after 6 months, while lower limb muscle mass significantly decreased. In the NO group, lumbar spine BMD and lower limb muscle mass did not significantly change after 6 months. In the OM group, BMD of the lumbar spine significantly increased but the lower limb muscle mass significantly decreased after 6 months relative to the NO group. In the combination therapy subgroup of the OM group muscle mass decreased significantly less than in the minodronate-alone subgroup. CONCLUSIONS: In postmenopausal women with osteoporosis, minodronate can increase BMD but cannot increase muscle mass. However, simultaneous use of activated vitamin D can suppress muscle mass decrease. The combination of activated vitamin D and minodronate may be useful for treating osteoporosis in postmenopausal women. The Japanese Society for Spine Surgery and Related Research 2018-02-28 /pmc/articles/PMC6698497/ /pubmed/31440661 http://dx.doi.org/10.22603/ssrr.2017-0016 Text en Copyright © 2018 by The Japanese Society for Spine Surgery and Related Research https://creativecommons.org/licenses/by-nc-nd/4.0/ Spine Surgery and Related Research 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
Fujimoto, Kazuki
Inage, Kazuhide
Toyoguchi, Toru
Eguchi, Yawara
Orita, Sumihisa
Yamauchi, Kazuyo
Suzuki, Miyako
Kubota, Gou
Sainoh, Takeshi
Sato, Jun
Shiga, Yasuhiro
Abe, Koki
Kanamoto, Hirohito
Inoue, Masahiro
Kinoshita, Hideyuki
Norimoto, Masaki
Umimura, Tomotaka
Koda, Masao
Furuya, Takeo
Nakamura, Junichi
Akazawa, Tsutomu
Terakado, Atsushi
Takahashi, Kazuhisa
Ohtori, Seiji
The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title_full The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title_fullStr The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title_full_unstemmed The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title_short The effects of minodronate and activated vitamin D on bone mineral density and muscle mass in postmenopausal women with osteoporosis
title_sort effects of minodronate and activated vitamin d on bone mineral density and muscle mass in postmenopausal women with osteoporosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698497/
https://www.ncbi.nlm.nih.gov/pubmed/31440661
http://dx.doi.org/10.22603/ssrr.2017-0016
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