Systematic Review: Efficacy of Medical Therapy on Outcomes Important to Pediatric Patients With X-Linked Hypophosphatemia

dc.contributor.authorAli, Dalal S.
dc.contributor.authorMirza, Reza D.
dc.contributor.authorHussein, Salma
dc.contributor.authorAlsarraf, Farah
dc.contributor.authorAlexander, R. Todd
dc.contributor.authorAlrob, Hajar Abu
dc.contributor.authorAppelman-Dijkstra, Natasha M.
dc.contributor.authorBiosse-Duplan, Martin
dc.contributor.authorBrandi, Maria Luisa
dc.contributor.authorCarpenter, Thomas O.
dc.contributor.authorChaussain, Catherine
dc.contributor.authorDandurand, Karel
dc.contributor.authorFiller, Guido
dc.contributor.authorFlorenzano, Pablo
dc.contributor.authorFukumoto, Seiji
dc.contributor.authorGrasemann, Corinna
dc.contributor.authorImel, Erik A.
dc.contributor.authorJan de Beur, Suzanne M.
dc.contributor.authorMorgante, Emmett
dc.contributor.authorWard, Leanne M.
dc.contributor.authorKhan, Aliya A.
dc.contributor.authorGuyatt, Gordon
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2025-05-13T11:23:21Z
dc.date.available2025-05-13T11:23:21Z
dc.date.issued2025
dc.description.abstractObjective: To examine the evidence addressing the management of X-linked hypophosphatemia (XLH) in children to inform treatment recommendations. Methods: 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. Results: 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. Conclusion: 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.
dc.eprint.versionFinal published version
dc.identifier.citationAli DS, Mirza RD, Hussein S, et al. Systematic Review: Efficacy of Medical Therapy on Outcomes Important to Pediatric Patients With X-Linked Hypophosphatemia. J Clin Endocrinol Metab. 2025;110(5):1205-1217. doi:10.1210/clinem/dgaf011
dc.identifier.urihttps://hdl.handle.net/1805/48027
dc.language.isoen_US
dc.publisherOxford University Press
dc.relation.isversionof10.1210/clinem/dgaf011
dc.relation.journalThe Journal of Clinical Endocrinology and Metabolism
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.subjectPediatric XLH
dc.subjectChildren XLH
dc.subjectEfficacy
dc.subjectBurosumab
dc.subjectConventional therapy
dc.subjectPatient-important outcomes
dc.titleSystematic Review: Efficacy of Medical Therapy on Outcomes Important to Pediatric Patients With X-Linked Hypophosphatemia
dc.typeArticle
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