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地诺单抗治疗脊髓性肌萎缩症男孩的严重废用性骨质疏松症

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

作者信息

Kutilek Stepan

机构信息

Department of Pediatrics, Pardubice Hospital, Pardubice, Czech Republic.

出版信息

Acta Med Iran. 2017 Oct;55(10):658-660.

Abstract

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.

摘要

地诺单抗是一种针对核因子κB受体活化因子配体的全人源重组单克隆抗体。地诺单抗用于治疗绝经后骨质疏松症和癌症相关的骨疾病。关于地诺单抗在儿童中的治疗数据非常稀少。一名14岁患有脊髓性肌萎缩症(SMA)和严重废用性骨质疏松症(脊柱骨密度L1-L4 BMD -6.2SD Z评分)且有两处常见脆性骨折的男孩接受了地诺单抗治疗。他在基线时和七个月后接受了60mg皮下注射。首次注射六个月后,L1-L4骨密度增加了19%。注射耐受性良好,无任何不良反应。血钙保持稳定(2.3 - 2.4mmol/L)。计划在六个月后进行第三次地诺单抗注射。在此之前,他患上了肺炎并因呼吸衰竭死亡,呼吸衰竭是SMA患者常见的死亡原因。这与地诺单抗治疗无关。总之,一剂地诺单抗显著增加了一名重度骨质疏松症儿童的骨密度。

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