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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Tehran University of Medical Sciences
2017-12-01
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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.
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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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1724522045249683456 |