Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study

Abstract Background Bisphosphonates are recommended for use as first-line therapy for the prevention and treatment of glucocorticoid-induced osteoporosis in adults. However, the appropriate usage of bisphosphonates for the prevention or treatment of glucocorticoid-induced osteoporosis in children re...

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Main Authors: Yuzaburo Inoue, Kanako Mitsunaga, Takeshi Yamamoto, Koki Chiba, Fumiya Yamaide, Taiji Nakano, Yoshinori Morita, Akiko Yamaide, Shuichi Suzuki, Takayasu Arima, Ken-ichi Yamaguchi, Minako Tomiita, Naoki Shimojo, Yoichi Kohno
Format: Article
Language:English
Published: BMC 2018-06-01
Series:Pediatric Rheumatology Online Journal
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Online Access:http://link.springer.com/article/10.1186/s12969-018-0258-5
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author Yuzaburo Inoue
Kanako Mitsunaga
Takeshi Yamamoto
Koki Chiba
Fumiya Yamaide
Taiji Nakano
Yoshinori Morita
Akiko Yamaide
Shuichi Suzuki
Takayasu Arima
Ken-ichi Yamaguchi
Minako Tomiita
Naoki Shimojo
Yoichi Kohno
author_facet Yuzaburo Inoue
Kanako Mitsunaga
Takeshi Yamamoto
Koki Chiba
Fumiya Yamaide
Taiji Nakano
Yoshinori Morita
Akiko Yamaide
Shuichi Suzuki
Takayasu Arima
Ken-ichi Yamaguchi
Minako Tomiita
Naoki Shimojo
Yoichi Kohno
author_sort Yuzaburo Inoue
collection DOAJ
description Abstract Background Bisphosphonates are recommended for use as first-line therapy for the prevention and treatment of glucocorticoid-induced osteoporosis in adults. However, the appropriate usage of bisphosphonates for the prevention or treatment of glucocorticoid-induced osteoporosis in children remains unclear. Methods We performed a cross-sectional study to clarify the factors associated with the development of glucocorticoid-induced bone loss and osteoporosis in patients with childhood-onset rheumatic disease and to investigate the impact of the early use of alendronate. We recruited 39 patients with childhood-onset rheumatic disease who were evaluated to detect bone loss or osteoporosis at 3 months to 1.5 years after the initiation of treatment. The primary outcome of the study was the presence of bone loss or osteoporosis at the initial evaluation of the bone mineral density after at least 3 months of glucocorticoid therapy. Results Bone loss and a history of fracture were found in 56 and 18% of the participants, respectively. Weekly oral alendronate therapy (median, 25.4 mg/m2) had been started by the time of the evaluation of osteoporosis in 46% of the participants and within 3 months after the start of glucocorticoid in 31% of the participants. There were no significant differences between the participants with bone loss (wBL group) and without bone loss (w/oBL group) in terms of gender, primary disease, or the age at the onset of primary disease. In terms of glucocorticoid use, there was no significant difference in the age at the start of glucocorticoid therapy, the length of glucocorticoid use, or the dose of glucocorticoids. The proportion of patients in the w/oBL group who received alendronate within 3 months after the start of glucocorticoid therapy was significantly greater than that in the wBL group. In the logistic regression analysis, only “alendronate therapy within 3 months after the start of glucocorticoid therapy” had a statistically significant effect on the development of bone loss (OR, 0.08; 95% CI, 0.02–0.43). The analysis did not reveal any factors associated with the development of osteoporosis. Conclusions The early use of alendronate may have a preventive effect against the development of bone loss in glucocorticoid-treated patients with childhood-onset rheumatic disease.
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spelling doaj.art-2b5054ef234d4399a5f93928e9b789b12022-12-22T02:55:49ZengBMCPediatric Rheumatology Online Journal1546-00962018-06-011611910.1186/s12969-018-0258-5Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional studyYuzaburo Inoue0Kanako Mitsunaga1Takeshi Yamamoto2Koki Chiba3Fumiya Yamaide4Taiji Nakano5Yoshinori Morita6Akiko Yamaide7Shuichi Suzuki8Takayasu Arima9Ken-ichi Yamaguchi10Minako Tomiita11Naoki Shimojo12Yoichi Kohno13Department of Pediatrics, Eastern Chiba Medical CenterDepartment of Pediatrics, Chiba Kaihin Municipal HospitalDepartment of Allergy and Rheumatology, Chiba Children’s HospitalDepartment of Traditional Medicine, Toho University Omori Medical CenterDepartment of Pediatrics, Graduate School of Medicine, Chiba UniversityDepartment of Pediatrics, Graduate School of Medicine, Chiba UniversityDepartment of Pediatrics, IMS Memorial HospitalDepartment of Allergy and Rheumatology, Chiba Children’s HospitalDepartment of Pediatrics, Shimoshizu National HospitalDepartment of Pediatrics, Kimitsu Chuo HospitalImmuno-Rheumatology Center, St.Luke’s Internationl HospitalDepartment of Allergy and Rheumatology, Chiba Children’s HospitalDepartment of Pediatrics, Graduate School of Medicine, Chiba UniversityChiba Rosai HospitalAbstract Background Bisphosphonates are recommended for use as first-line therapy for the prevention and treatment of glucocorticoid-induced osteoporosis in adults. However, the appropriate usage of bisphosphonates for the prevention or treatment of glucocorticoid-induced osteoporosis in children remains unclear. Methods We performed a cross-sectional study to clarify the factors associated with the development of glucocorticoid-induced bone loss and osteoporosis in patients with childhood-onset rheumatic disease and to investigate the impact of the early use of alendronate. We recruited 39 patients with childhood-onset rheumatic disease who were evaluated to detect bone loss or osteoporosis at 3 months to 1.5 years after the initiation of treatment. The primary outcome of the study was the presence of bone loss or osteoporosis at the initial evaluation of the bone mineral density after at least 3 months of glucocorticoid therapy. Results Bone loss and a history of fracture were found in 56 and 18% of the participants, respectively. Weekly oral alendronate therapy (median, 25.4 mg/m2) had been started by the time of the evaluation of osteoporosis in 46% of the participants and within 3 months after the start of glucocorticoid in 31% of the participants. There were no significant differences between the participants with bone loss (wBL group) and without bone loss (w/oBL group) in terms of gender, primary disease, or the age at the onset of primary disease. In terms of glucocorticoid use, there was no significant difference in the age at the start of glucocorticoid therapy, the length of glucocorticoid use, or the dose of glucocorticoids. The proportion of patients in the w/oBL group who received alendronate within 3 months after the start of glucocorticoid therapy was significantly greater than that in the wBL group. In the logistic regression analysis, only “alendronate therapy within 3 months after the start of glucocorticoid therapy” had a statistically significant effect on the development of bone loss (OR, 0.08; 95% CI, 0.02–0.43). The analysis did not reveal any factors associated with the development of osteoporosis. Conclusions The early use of alendronate may have a preventive effect against the development of bone loss in glucocorticoid-treated patients with childhood-onset rheumatic disease.http://link.springer.com/article/10.1186/s12969-018-0258-5OsteoporosisBone lossAlendronateGlucocorticoidChildhood-onset rheumatic disease
spellingShingle Yuzaburo Inoue
Kanako Mitsunaga
Takeshi Yamamoto
Koki Chiba
Fumiya Yamaide
Taiji Nakano
Yoshinori Morita
Akiko Yamaide
Shuichi Suzuki
Takayasu Arima
Ken-ichi Yamaguchi
Minako Tomiita
Naoki Shimojo
Yoichi Kohno
Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
Pediatric Rheumatology Online Journal
Osteoporosis
Bone loss
Alendronate
Glucocorticoid
Childhood-onset rheumatic disease
title Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
title_full Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
title_fullStr Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
title_full_unstemmed Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
title_short Early use of alendronate as a protective factor against the development of glucocorticoid-induced bone loss in childhood-onset rheumatic diseases: a cross-sectional study
title_sort early use of alendronate as a protective factor against the development of glucocorticoid induced bone loss in childhood onset rheumatic diseases a cross sectional study
topic Osteoporosis
Bone loss
Alendronate
Glucocorticoid
Childhood-onset rheumatic disease
url http://link.springer.com/article/10.1186/s12969-018-0258-5
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