Ali Dalal S, Mirza Reza D, Hussein Salma, Alsarraf Farah, Alexander R Todd, Abu Alrob Hajar, Appelman-Dijkstra Natasha M, Biosse-Duplan Martin, Brandi Maria Luisa, Carpenter Thomas O, Chaussain Catherine, Dandurand Karel, Filler Guido, Florenzano Pablo, Fukumoto Seiji, Grasemann Corinna, Imel Erik A, Jan de Beur Suzanne M, Morgante Emmett, Ward Leanne M, Khan Aliya A, Guyatt Gordon
Division of Endocrinology and Metabolism, McMaster University, Hamilton, ON, Canada L8S 4L8.
Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada L8S 4L8.
J Clin Endocrinol Metab. 2025 Apr 22;110(5):1205-1217. doi: 10.1210/clinem/dgaf011.
To examine the evidence addressing the management of X-linked hypophosphatemia (XLH) in children to inform treatment recommendations.
We searched Embase, MEDLINE, Web of Science, and Cochrane Central up to May 2023. Eligible studies included randomized controlled trials (RCTs) and observational studies of individuals younger than 18 years with clinically or genetically confirmed XLH. Manuscripts comparing burosumab to either no treatment or conventional therapy (phosphate and active vitamin D) or evaluating conventional therapy to no treatment were included. Two reviewers independently determined eligibility, extracted data, and assessed risk of bias (RoB). GRADE methodology was used to assess evidence certainty.
We screened 4114 records and assessed 254 full texts. One RCT and one post hoc study proved eligible when comparing burosumab to conventional therapy or no treatment. The open-label RCT was at high RoB, with certainty of evidence ranging from moderate to very low. Burosumab, compared to conventional therapy, probably prevents lower limb deformity and improves physical health quality of life (QoL) (moderate certainty). Burosumab may increase height and enhance the burden of symptoms related to chronic hypophosphatemia (low certainty). Burosumab probably increases treatment-emergent adverse events (moderate certainty) and may increase dental abscesses (low certainty). One observational study assessing conventional therapy vs no treatment was at high RoB, providing very low certainty evidence regarding the impact of conventional therapy on final height.
Our review indicates that burosumab likely provides benefits to children by preventing lower limb deformity and improving physical health QoL while potentially increasing height. However, burosumab may also increase adverse events. Our review found limited evidence regarding the impact of conventional therapy compared to no treatment on final height. Further research is required to understand the long-term effect of medical therapy in children.
研究关于儿童X连锁低磷血症(XLH)管理的证据,为治疗建议提供依据。
截至2023年5月,我们检索了Embase、MEDLINE、Web of Science和Cochrane Central。符合条件的研究包括针对18岁以下临床或基因确诊XLH个体的随机对照试验(RCT)和观察性研究。纳入比较布罗索尤单抗与未治疗或传统疗法(磷酸盐和活性维生素D)的手稿,或评估传统疗法与未治疗对比的手稿。两名 reviewers 独立确定纳入资格、提取数据并评估偏倚风险(RoB)。采用GRADE方法评估证据确定性。
我们筛选了4114条记录并评估了254篇全文。在比较布罗索尤单抗与传统疗法或未治疗时,一项RCT和一项事后分析研究符合条件。开放标签RCT的RoB较高,证据确定性从中度到极低。与传统疗法相比,布罗索尤单抗可能预防下肢畸形并改善身体健康生活质量(QoL)(中度确定性)。布罗索尤单抗可能增加身高并加重与慢性低磷血症相关的症状负担(低确定性)。布罗索尤单抗可能增加治疗中出现的不良事件(中度确定性),并可能增加牙脓肿(低确定性)。一项评估传统疗法与未治疗对比的观察性研究的RoB较高,提供了关于传统疗法对最终身高影响的极低确定性证据。
我们的综述表明,布罗索尤单抗可能通过预防下肢畸形和改善身体健康QoL为儿童带来益处,同时可能增加身高。然而,布罗索尤单抗也可能增加不良事件。我们的综述发现,与未治疗相比,关于传统疗法对最终身高影响的证据有限。需要进一步研究以了解儿童药物治疗的长期效果。