一名患有 FGF23 相关性低磷血症的患者在接受矫正截骨术后,通过短期布罗苏单抗治疗实现了有效的骨愈合。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Hsin-Sung Chiu, Meng-Ju Melody Tsai, Ting-Ming Wang, Ni-Chung Lee, Yi-Ching Tung
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引用次数: 0

摘要

低磷血症性佝偻病是一种罕见的代谢性骨病,由肾脏磷酸盐消耗引起,导致骨矿化障碍。我们报告了一例成纤维细胞生长因子 23(FGF23)相关性低磷血症佝偻病男孩的病例,他在矫正截骨术后接受了六个月的磷酸盐和活性维生素 D 传统治疗,但胼胝体仍未得到巩固。使用 FGF23 抗体(burosumab)治疗一个月后,患者的病情有了明显改善,不再需要助行器。在接受布罗苏单抗治疗 6 个月后,骨骼几乎完全愈合。本报告首次论述了骨科手术后短期使用布罗苏单抗疗法促进骨愈合的问题。我们的研究结果进一步强调了布罗苏单抗在治疗与 FGF23 相关的低磷酸盐血症方面的临床优势和短期应用,尤其是对于接受骨科手术的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effective bone healing after corrective osteotomy in a patient with FGF23-related hypophosphatemic disease using short-term burosumab treatment.

Hypophosphatemic rickets is a rare metabolic bone disease caused by renal phosphate wasting, leading to impaired bone mineralization. We present a case of a boy with fibroblast growth factor 23 (FGF23)-related hypophosphatemic rickets who did not achieve callus consolidation after six months of conventional therapy with phosphate and active vitamin D following corrective osteotomy. After one month of therapy with an FGF23 antibody (burosumab), the patient demonstrated significant improvement and no longer required a walking aid. Following six months of burosumab therapy, the bone had nearly fully healed. This report is the first to address the short-term use of burosumab therapy to promote bone healing after orthopedic surgery. Our findings further emphasize the clinical advantages and short-term applications of burosumab in FGF23-related hypophosphatemic diseases, especially for patients undergoing orthopedic surgery.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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