Department of Orthopaedic Surgery, Aichi Children's Health and Medical Center, Obu.
Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya.
J Pediatr Orthop B. 2024 Jan 1;33(1):90-96. doi: 10.1097/BPB.0000000000001054. Epub 2022 Dec 26.
Fibroblast growth factor 23 (FGF23)-related hypophosphatemic rickets (HPR) are characterized by excess circulating FGF23 and low concentrations of serum phosphorus, leading to skeletal manifestations of rickets, including lower limb deformities in children. The objective of this study was to prospectively evaluate whether treatment with burosumab, a monoclonal antibody neutralizing FGF23, changes lower limb deformities in HPR. Patients who were 15 years of age or younger with a documented clinical diagnosis of HPR, receiving burosumab treatment, and had a minimum follow-up period of one year were included in the study. Various radiological parameters were measured from anteroposterior and lateral radiographs of the bilateral lower limbs taken before administration of burosumab and at 3, 6, 9, and 12 months after treatment for evaluation of lower limb alignment. Outcome was classified as 'improvement', 'no change', or 'deterioration' after 12 months treatment. Five patients (10 limbs), with a mean age of 7.2 years were included in this study. The outcome was 'improvement' in six limbs and 'no change' in four limbs. There were no limbs of 'deterioration'. The improvement in deformities after treatment was more significant in younger patients who originally showed severe lower limb deformities. Older patients with milder deformities, on the other hand, showed less improvement. Burosumab therapy favorably changed lower-limb malalignment in children with FGF23-related HPR.
成纤维细胞生长因子 23(FGF23)相关低磷血症性佝偻病(HPR)的特征是循环中 FGF23 过多和血清磷浓度降低,导致佝偻病的骨骼表现,包括儿童下肢畸形。本研究的目的是前瞻性评估成纤维细胞生长因子 23 中和单克隆抗体布罗索尤单抗治疗是否能改变 HPR 中的下肢畸形。本研究纳入了年龄在 15 岁及以下、有明确 HPR 临床诊断、接受布罗索尤单抗治疗且随访时间至少 1 年的患者。从双侧下肢前后位和侧位 X 光片测量各种影像学参数,在布罗索尤单抗治疗前和治疗后 3、6、9 和 12 个月进行评估,以评估下肢对线。根据 12 个月治疗后的结果将结局分为“改善”、“无变化”或“恶化”。本研究纳入了 5 名(10 条肢体)患者,平均年龄为 7.2 岁。6 条肢体的结局为“改善”,4 条肢体为“无变化”。没有肢体“恶化”。在最初表现出严重下肢畸形的年轻患者中,治疗后畸形的改善更为显著。另一方面,畸形较轻的老年患者的改善较少。布罗索尤单抗治疗可显著改善 FGF23 相关 HPR 儿童的下肢对线不良。