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Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss
Bisphosphonate is widely used to treat patients with primary and secondary osteoporosis. The chronic administration of furosemide is considered a risk factor for osteoporosis mainly due to the increased urinary excretion of calcium, leading to a long-term negative balance of calcium. We describe two...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society for Pediatric Endocrinology
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004841/ https://www.ncbi.nlm.nih.gov/pubmed/24790329 http://dx.doi.org/10.1297/cpe.15.101 |
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author | Kubota, Takuo Namba, Noriyuki Kurotobi, Shunji Kogaki, Shigetoyo Hirai, Haruhiko Kitaoka, Taichi Nakajima, Shigeo Ozono, Keiichi |
author_facet | Kubota, Takuo Namba, Noriyuki Kurotobi, Shunji Kogaki, Shigetoyo Hirai, Haruhiko Kitaoka, Taichi Nakajima, Shigeo Ozono, Keiichi |
author_sort | Kubota, Takuo |
collection | PubMed |
description | Bisphosphonate is widely used to treat patients with primary and secondary osteoporosis. The chronic administration of furosemide is considered a risk factor for osteoporosis mainly due to the increased urinary excretion of calcium, leading to a long-term negative balance of calcium. We describe two patients with mild heart failure who took furosemide for more than 5 yr and developed hyperparathyroidism and lumbago associated with low bone mineral density. Their serum levels of intact parathyroid hormone and bone mineral density (BMD) of the lumbar spine (L2-L4) were 180.8 and 144.3 pg/ml, and 71% and 80% of the mean of healthy women, respectively. The oral administration of alendronate or risedronate was effective for lumbago and improved BMD, although the urinary excretion of calcium and hyperparathyroidism were not changed. For the medical treatment of lumbago and decreased bone mass secondary to the long-term administration of furosemide, bisphosphonate is proposed when the dose of furosemide cannot be reduced. However, it may be important to give sufficient calcium and vitamin D to patients to improve secondary hyperparathyroidism. |
format | Online Article Text |
id | pubmed-4004841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Japanese Society for Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
spelling | pubmed-40048412014-04-30 Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss Kubota, Takuo Namba, Noriyuki Kurotobi, Shunji Kogaki, Shigetoyo Hirai, Haruhiko Kitaoka, Taichi Nakajima, Shigeo Ozono, Keiichi Clin Pediatr Endocrinol Original Article Bisphosphonate is widely used to treat patients with primary and secondary osteoporosis. The chronic administration of furosemide is considered a risk factor for osteoporosis mainly due to the increased urinary excretion of calcium, leading to a long-term negative balance of calcium. We describe two patients with mild heart failure who took furosemide for more than 5 yr and developed hyperparathyroidism and lumbago associated with low bone mineral density. Their serum levels of intact parathyroid hormone and bone mineral density (BMD) of the lumbar spine (L2-L4) were 180.8 and 144.3 pg/ml, and 71% and 80% of the mean of healthy women, respectively. The oral administration of alendronate or risedronate was effective for lumbago and improved BMD, although the urinary excretion of calcium and hyperparathyroidism were not changed. For the medical treatment of lumbago and decreased bone mass secondary to the long-term administration of furosemide, bisphosphonate is proposed when the dose of furosemide cannot be reduced. However, it may be important to give sufficient calcium and vitamin D to patients to improve secondary hyperparathyroidism. The Japanese Society for Pediatric Endocrinology 2006-08-02 2006 /pmc/articles/PMC4004841/ /pubmed/24790329 http://dx.doi.org/10.1297/cpe.15.101 Text en 2006©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Article Kubota, Takuo Namba, Noriyuki Kurotobi, Shunji Kogaki, Shigetoyo Hirai, Haruhiko Kitaoka, Taichi Nakajima, Shigeo Ozono, Keiichi Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss |
title | Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by
Chronic Administration of Furosemide without Alteration of Its Administration and Urinary
Calcium Loss |
title_full | Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by
Chronic Administration of Furosemide without Alteration of Its Administration and Urinary
Calcium Loss |
title_fullStr | Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by
Chronic Administration of Furosemide without Alteration of Its Administration and Urinary
Calcium Loss |
title_full_unstemmed | Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by
Chronic Administration of Furosemide without Alteration of Its Administration and Urinary
Calcium Loss |
title_short | Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by
Chronic Administration of Furosemide without Alteration of Its Administration and Urinary
Calcium Loss |
title_sort | beneficial effect of oral bisphosphonate treatment on bone loss induced by
chronic administration of furosemide without alteration of its administration and urinary
calcium loss |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004841/ https://www.ncbi.nlm.nih.gov/pubmed/24790329 http://dx.doi.org/10.1297/cpe.15.101 |
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