期刊
CURRENT OSTEOPOROSIS REPORTS
卷 19, 期 3, 页码 271-277出版社
SPRINGER
DOI: 10.1007/s11914-021-00669-9
关键词
X-Linked hypophosphatemia; Burosumab; FGF23; Rickets
资金
- National Institutes of Health through NIAMS [P30AR072581]
X-Linked hypophosphatemia (XLH) is the most common genetic cause of rickets, and treatment with burosumab has shown significant improvements in both children and adults. However, many questions remain regarding its impact on various outcomes.
Purpose of Review X-Linked hypophosphatemia (XLH) is the most common genetic cause of rickets. This review describes advances in the management of XLH using burosumab which was FDA approved for treating children with XLH in 2018. Recent Findings Elevated FGF23 in XLH leads to systemic hypophosphatemia and several musculoskeletal manifestations, including rachitic bone deformities, impaired growth, dental abscesses, insufficiency fractures, osteoarthritis, and enthesopathy, with lifelong consequences for physical function and quality of life. Burosumab treatment has demonstrated clinical improvement of rickets and growth in children, including during a randomized controlled trial compared with conventional therapy. Burosumab also improved pseudofracture healing in adults. Burosumab led to greater improvement in rickets and growth than conventional therapy. However, many questions remain regarding the impact of burosumab on several outcomes, including final height, nephrocalcinosis, dental disease, enthesopathy, and surgical interventions.
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