Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy

Denosumab is a fully human recombinant monoclonal antibody to the receptor activator of nuclear factor-κB ligand. Denosumab is used in the treatment of postmenopausal osteoporosis and cancer-related bone disorders. There are only very scarce data on denosumab treatment in children. 14-year-old boy...

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Main Author: Stepan Kutilek
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2017-12-01
Series:Acta Medica Iranica
Subjects:
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/5707
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spelling doaj-4a066a61feed4dcc9691c1fb087822902020-11-25T03:43:00ZengTehran University of Medical SciencesActa Medica Iranica0044-60251735-96942017-12-0155105220Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular AtrophyStepan Kutilek0Department of Pediatrics, Pardubice Hospital, Pardubice, Czech Republic. Denosumab is a fully human recombinant monoclonal antibody to the receptor activator of nuclear factor-κB ligand. Denosumab is used in the treatment of postmenopausal osteoporosis and cancer-related bone disorders. There are only very scarce data on denosumab treatment in children. 14-year-old boy with spinal muscular atrophy (SMA) and severe disuse osteoporosis (spinal bone mineral density L1-L4 BMD-6.2SD Z-score) and two prevalent fragility fractures was treated with denosumab. He received 60 mg  subcutaneous injection at the baseline and seven months later. Six months after the initial injection there was a 19% increase in L1-L4 BMD. The injections were well tolerated without any adverse reactions. Calcemia remained stable (2.3-2.4 mmol/L). He was scheduled for the third denosumab injection six months later. Prior to this date, he acquired pneumonia and died due to respiratory failure, which is a frequent cause of death in patients with SMA. There was no relation to the denosumab treatment. In conclusion, one dose of denosumab significantly increased BMD in a child with severe osteoporosis. https://acta.tums.ac.ir/index.php/acta/article/view/5707DenosumabSpinal muscular atrophyFracturesBoneOsteoporosisBone mineral density
collection DOAJ
language English
format Article
sources DOAJ
author Stepan Kutilek
spellingShingle Stepan Kutilek
Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
Acta Medica Iranica
Denosumab
Spinal muscular atrophy
Fractures
Bone
Osteoporosis
Bone mineral density
author_facet Stepan Kutilek
author_sort Stepan Kutilek
title Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
title_short Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
title_full Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
title_fullStr Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
title_full_unstemmed Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy
title_sort denosumab treatment of severe disuse osteoporosis in a boy with spinal muscular atrophy
publisher Tehran University of Medical Sciences
series Acta Medica Iranica
issn 0044-6025
1735-9694
publishDate 2017-12-01
description Denosumab is a fully human recombinant monoclonal antibody to the receptor activator of nuclear factor-κB ligand. Denosumab is used in the treatment of postmenopausal osteoporosis and cancer-related bone disorders. There are only very scarce data on denosumab treatment in children. 14-year-old boy with spinal muscular atrophy (SMA) and severe disuse osteoporosis (spinal bone mineral density L1-L4 BMD-6.2SD Z-score) and two prevalent fragility fractures was treated with denosumab. He received 60 mg  subcutaneous injection at the baseline and seven months later. Six months after the initial injection there was a 19% increase in L1-L4 BMD. The injections were well tolerated without any adverse reactions. Calcemia remained stable (2.3-2.4 mmol/L). He was scheduled for the third denosumab injection six months later. Prior to this date, he acquired pneumonia and died due to respiratory failure, which is a frequent cause of death in patients with SMA. There was no relation to the denosumab treatment. In conclusion, one dose of denosumab significantly increased BMD in a child with severe osteoporosis.
topic Denosumab
Spinal muscular atrophy
Fractures
Bone
Osteoporosis
Bone mineral density
url https://acta.tums.ac.ir/index.php/acta/article/view/5707
work_keys_str_mv AT stepankutilek denosumabtreatmentofseveredisuseosteoporosisinaboywithspinalmuscularatrophy
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