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Alendronate improves QOL of postmenopausal women with osteoporosis

PURPOSE: Postmenopausal osteoporosis causes bone fracture as well as pain, physical, psychological and socially adverse effects, which affects a patient’s quality of life (QOL). The effect of alendronate on QOL was investigated compared with that of alfacalcidol in post-menopausal osteoporotic women...

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Autores principales: Kawate, Hisaya, Ohnaka, Keizo, Adachi, Masahiro, Kono, Suminori, Ikematsu, Hideyuki, Matsuo, Hisashi, Higuchi, Kazumi, Takayama, Takehiko, Takayanagi, Ryoichi
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861847/
https://www.ncbi.nlm.nih.gov/pubmed/20458350
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author Kawate, Hisaya
Ohnaka, Keizo
Adachi, Masahiro
Kono, Suminori
Ikematsu, Hideyuki
Matsuo, Hisashi
Higuchi, Kazumi
Takayama, Takehiko
Takayanagi, Ryoichi
author_facet Kawate, Hisaya
Ohnaka, Keizo
Adachi, Masahiro
Kono, Suminori
Ikematsu, Hideyuki
Matsuo, Hisashi
Higuchi, Kazumi
Takayama, Takehiko
Takayanagi, Ryoichi
author_sort Kawate, Hisaya
collection PubMed
description PURPOSE: Postmenopausal osteoporosis causes bone fracture as well as pain, physical, psychological and socially adverse effects, which affects a patient’s quality of life (QOL). The effect of alendronate on QOL was investigated compared with that of alfacalcidol in post-menopausal osteoporotic women. PATIENTS AND METHODS: A total of 44 postmenopausal osteoporotic women (mean age 69.8 years) with back or joint pain, although capable of walking, were randomly assigned to two groups; group A (n = 25) received 5 mg/day of alendronate, and group B (n = 19) received 0.5 μg/day of alfacalcidol, for the first 4 months. For the following 2 months, the group A received 0.5 μg/day of alfacalcidol and the group B received 5 mg/day of alendronate in a crossover design. The patient’s QOL was evaluated by score of Japanese Osteoporosis Quality of Life Questionnaire (JOQOL), and pain intensity using a visual analog scale (VAS). Bone metabolism was measured by bone mineral density (BMD) and a biomarker for bone resorption, urinary crosslinked N-terminal telopeptide of type I collagen (NTX). RESULTS: With 4-month treatment, alendronate, but not alfacalcidol, improved pain-related QOL, reduced joint pain by VAS, and increased bone mineral density. Both treatments significantly reduced bone resorption, the inhibition was significantly higher with alendronate (−56.5%) compared with alfacalcidol (−18.1%). After crossover, the patients in group A received alfacalcidol and had a reduced total and daily living activity-related QOL scores, and increased upper back pain by VAS. The group B received alendronate had significantly reduced bone resorption after the 2 months. CONCLUSION: Alendronate improves the QOL of Japanese postmenopausal women with osteoporosis by reducing pain intensity as well as increasing bone mineral density.
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spelling pubmed-28618472010-05-10 Alendronate improves QOL of postmenopausal women with osteoporosis Kawate, Hisaya Ohnaka, Keizo Adachi, Masahiro Kono, Suminori Ikematsu, Hideyuki Matsuo, Hisashi Higuchi, Kazumi Takayama, Takehiko Takayanagi, Ryoichi Clin Interv Aging Original Research PURPOSE: Postmenopausal osteoporosis causes bone fracture as well as pain, physical, psychological and socially adverse effects, which affects a patient’s quality of life (QOL). The effect of alendronate on QOL was investigated compared with that of alfacalcidol in post-menopausal osteoporotic women. PATIENTS AND METHODS: A total of 44 postmenopausal osteoporotic women (mean age 69.8 years) with back or joint pain, although capable of walking, were randomly assigned to two groups; group A (n = 25) received 5 mg/day of alendronate, and group B (n = 19) received 0.5 μg/day of alfacalcidol, for the first 4 months. For the following 2 months, the group A received 0.5 μg/day of alfacalcidol and the group B received 5 mg/day of alendronate in a crossover design. The patient’s QOL was evaluated by score of Japanese Osteoporosis Quality of Life Questionnaire (JOQOL), and pain intensity using a visual analog scale (VAS). Bone metabolism was measured by bone mineral density (BMD) and a biomarker for bone resorption, urinary crosslinked N-terminal telopeptide of type I collagen (NTX). RESULTS: With 4-month treatment, alendronate, but not alfacalcidol, improved pain-related QOL, reduced joint pain by VAS, and increased bone mineral density. Both treatments significantly reduced bone resorption, the inhibition was significantly higher with alendronate (−56.5%) compared with alfacalcidol (−18.1%). After crossover, the patients in group A received alfacalcidol and had a reduced total and daily living activity-related QOL scores, and increased upper back pain by VAS. The group B received alendronate had significantly reduced bone resorption after the 2 months. CONCLUSION: Alendronate improves the QOL of Japanese postmenopausal women with osteoporosis by reducing pain intensity as well as increasing bone mineral density. Dove Medical Press 2010 2010-04-26 /pmc/articles/PMC2861847/ /pubmed/20458350 Text en © 2010 Kawate et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Kawate, Hisaya
Ohnaka, Keizo
Adachi, Masahiro
Kono, Suminori
Ikematsu, Hideyuki
Matsuo, Hisashi
Higuchi, Kazumi
Takayama, Takehiko
Takayanagi, Ryoichi
Alendronate improves QOL of postmenopausal women with osteoporosis
title Alendronate improves QOL of postmenopausal women with osteoporosis
title_full Alendronate improves QOL of postmenopausal women with osteoporosis
title_fullStr Alendronate improves QOL of postmenopausal women with osteoporosis
title_full_unstemmed Alendronate improves QOL of postmenopausal women with osteoporosis
title_short Alendronate improves QOL of postmenopausal women with osteoporosis
title_sort alendronate improves qol of postmenopausal women with osteoporosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861847/
https://www.ncbi.nlm.nih.gov/pubmed/20458350
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