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Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study
BACKGROUND AND AIMS: Clinical data regarding alendronate jelly are limited. We compared the efficacy and safety of once‐weekly alendronate oral jelly with once‐weekly alendronate tablet formulations in the context of primary osteoporosis. METHODS: In this 6‐month, open‐label, prospective, observatio...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346986/ https://www.ncbi.nlm.nih.gov/pubmed/30697599 http://dx.doi.org/10.1002/hsr2.107 |
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author | Okimoto, Nobukazu Uemura, Yukari Yoshioka, Toru Arita, Shinobu Tsurukami, Hiroshi Otomo, Hajime Nishida, Satoshi Ogawa, Takayuki Hirao, Ken Ikeda, Satoshi Matsumoto, Hidehiro Toten, Yoriko Katae, Yuji Okazaki, Yuichi Nakagawa, Tsuyoshi Sakai, Akinori |
author_facet | Okimoto, Nobukazu Uemura, Yukari Yoshioka, Toru Arita, Shinobu Tsurukami, Hiroshi Otomo, Hajime Nishida, Satoshi Ogawa, Takayuki Hirao, Ken Ikeda, Satoshi Matsumoto, Hidehiro Toten, Yoriko Katae, Yuji Okazaki, Yuichi Nakagawa, Tsuyoshi Sakai, Akinori |
author_sort | Okimoto, Nobukazu |
collection | PubMed |
description | BACKGROUND AND AIMS: Clinical data regarding alendronate jelly are limited. We compared the efficacy and safety of once‐weekly alendronate oral jelly with once‐weekly alendronate tablet formulations in the context of primary osteoporosis. METHODS: In this 6‐month, open‐label, prospective, observational study, Japanese patients aged ≥60 years with primary osteoporosis were included from 14 primary care centres in Japan. The effects of once‐weekly alendronate oral jelly and tablet formulations on bone mineral density (BMD), bone turnover markers, and quality of life related to gastrointestinal symptoms were assessed at baseline and 6 months. Treatment was allocated by patient preference. This potentially confounding factor was adjusted for statistically. RESULTS: In total, 170 patients were enrolled (jelly, n = 97; tablet, n = 73). Mean percent changes in radius, lumbar spine, femoral neck, and hip BMD were similar in both treatment groups at 6 months. Both formulations decreased tartrate‐resistant acid phosphatase 5b (TRACP‐5b) and procollagen 1 N‐terminal peptide (P1NP) between baseline and 6 months (by about 50% and 60%, respectively); no significant differences in mean changes were noted in these markers between groups. At 6 months, no significant differences were noted in visual analogue scale or EuroQOL five‐dimension questionnaire scores between groups. The jelly group had significantly lower scores than the tablet group in the Izumo scale domains of heartburn (−0.81, P = 0.0040), epigastralgia (−0.94, P = 0.0003), and epigastric fullness (−0.49, P = 0.044). During treatment, more patients discontinued for upper gastrointestinal symptoms in the tablet group (n = 4) than the jelly group (n = 1). CONCLUSIONS: Once‐weekly alendronate oral jelly 35 mg may be a suitable alternative therapeutic agent for primary osteoporosis in Japan. |
format | Online Article Text |
id | pubmed-6346986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63469862019-01-29 Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study Okimoto, Nobukazu Uemura, Yukari Yoshioka, Toru Arita, Shinobu Tsurukami, Hiroshi Otomo, Hajime Nishida, Satoshi Ogawa, Takayuki Hirao, Ken Ikeda, Satoshi Matsumoto, Hidehiro Toten, Yoriko Katae, Yuji Okazaki, Yuichi Nakagawa, Tsuyoshi Sakai, Akinori Health Sci Rep Research Articles BACKGROUND AND AIMS: Clinical data regarding alendronate jelly are limited. We compared the efficacy and safety of once‐weekly alendronate oral jelly with once‐weekly alendronate tablet formulations in the context of primary osteoporosis. METHODS: In this 6‐month, open‐label, prospective, observational study, Japanese patients aged ≥60 years with primary osteoporosis were included from 14 primary care centres in Japan. The effects of once‐weekly alendronate oral jelly and tablet formulations on bone mineral density (BMD), bone turnover markers, and quality of life related to gastrointestinal symptoms were assessed at baseline and 6 months. Treatment was allocated by patient preference. This potentially confounding factor was adjusted for statistically. RESULTS: In total, 170 patients were enrolled (jelly, n = 97; tablet, n = 73). Mean percent changes in radius, lumbar spine, femoral neck, and hip BMD were similar in both treatment groups at 6 months. Both formulations decreased tartrate‐resistant acid phosphatase 5b (TRACP‐5b) and procollagen 1 N‐terminal peptide (P1NP) between baseline and 6 months (by about 50% and 60%, respectively); no significant differences in mean changes were noted in these markers between groups. At 6 months, no significant differences were noted in visual analogue scale or EuroQOL five‐dimension questionnaire scores between groups. The jelly group had significantly lower scores than the tablet group in the Izumo scale domains of heartburn (−0.81, P = 0.0040), epigastralgia (−0.94, P = 0.0003), and epigastric fullness (−0.49, P = 0.044). During treatment, more patients discontinued for upper gastrointestinal symptoms in the tablet group (n = 4) than the jelly group (n = 1). CONCLUSIONS: Once‐weekly alendronate oral jelly 35 mg may be a suitable alternative therapeutic agent for primary osteoporosis in Japan. John Wiley and Sons Inc. 2018-12-12 /pmc/articles/PMC6346986/ /pubmed/30697599 http://dx.doi.org/10.1002/hsr2.107 Text en © 2018 The Authors. Health Science Reports published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Okimoto, Nobukazu Uemura, Yukari Yoshioka, Toru Arita, Shinobu Tsurukami, Hiroshi Otomo, Hajime Nishida, Satoshi Ogawa, Takayuki Hirao, Ken Ikeda, Satoshi Matsumoto, Hidehiro Toten, Yoriko Katae, Yuji Okazaki, Yuichi Nakagawa, Tsuyoshi Sakai, Akinori Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title | Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title_full | Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title_fullStr | Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title_full_unstemmed | Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title_short | Treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for Japanese patients with primary osteoporosis: An open‐label, prospective, observational study |
title_sort | treatment with once‐weekly alendronate oral jelly compared with once‐weekly alendronate oral tablet for japanese patients with primary osteoporosis: an open‐label, prospective, observational study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346986/ https://www.ncbi.nlm.nih.gov/pubmed/30697599 http://dx.doi.org/10.1002/hsr2.107 |
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