# The lived experience of adolescents with X-linked hypophosphataemia treated with burosumab at end of skeletal growth: a mixed-methods analysis

**Authors:** Vrinda Saraff, Pedro Arango Sancho, Justine Bacchetta, Annemieke M. Boot, Christine Burren, Amish Chinoy, Poonam Dharmaraj, Maria Amelia Gómez Llorente, Juan David González Rodríguez, Iva Gueorguieva, Elin Haf Davies, Wesley Hayes, Sandra Komarzynski, Héctor Ríos Duro, Angela J. Rylands, Kerry Sandilands, Angela Williams, Emily Hardie, Haruka Ishii, Dirk Schnabel, Santhani M. Selveindran, Agnès Linglart

PMC · DOI: 10.1371/journal.pone.0344902 · 2026-03-20

## TL;DR

This study explores how adolescents with a rare genetic disorder feel and function while on a specific treatment before their bones stop growing.

## Contribution

The study provides new insights into adolescents' lived experiences with XLH and burosumab treatment at the end of skeletal growth.

## Key findings

- Low median symptom severity scores for pain, stiffness, and fatigue were reported.
- Symptoms were often triggered by physical activity but rarely disrupted daily life.
- Some adolescents experienced emotional concerns related to treatment transition.

## Abstract

X-linked hypophosphataemia is a rare, genetic, lifelong disorder caused by phosphate-regulating endopeptidase homologue X-linked pathogenic variants and, if left untreated, is associated with a progressive accumulation of musculoskeletal manifestations. Burosumab is a fully human monoclonal antibody that targets circulating fibroblast growth factor 23 and directly inhibits its activity, thereby correcting the abnormal phosphate homoeostasis in people with X-linked hypophosphataemia (XLH). The efficacy and safety of burosumab has been demonstrated in a programme of clinical trials in children and adults. Few data describe the experience of adolescents with XLH receiving burosumab treatment before and after skeletal growth ends. This prospective, multicentre, mixed-methods study described the lived experience of adolescents with XLH treated with burosumab at the end of skeletal growth (NCT05181839). Using patient-reported outcomes, wearable devices, and interviews, we found low median symptom severity scores for pain (0.00), stiffness (0.00), and fatigue (1.75) on a 0–10 scale. Symptoms were usually triggered by physical activity but rarely interfered with daily life. Some adolescents reported emotional concerns related to XLH and treatment transition. These insights can inform patient support during transition to adult care.

## Linked entities

- **Diseases:** XLH (MONDO:0010619)

## Full-text entities

- **Genes:** PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, FGF23 (fibroblast growth factor 23) [NCBI Gene 8074] {aka ADHR, FGFN, HFTC2, HPDR2, HYPF, PHPTC}, PHEX (phosphate regulating endopeptidase X-linked) [NCBI Gene 5251] {aka HPDR, HPDR1, HYP, HYP1, LXHR, PEX}
- **Diseases:** X-linked hypophosphataemia (MESH:C536424), enthesopathies (MESH:D000070676), impaired mobility (MESH:D014086), dental abscesses (MESH:D000038), depression (MESH:D003866), bruise (MESH:D003288), nephrocalcinosis (MESH:D009397), muscle weakness (MESH:D018908), muscle (MESH:D019042), Pain (MESH:D010146), Stiffness (MESH:C566112), osteoarthritis (MESH:D010003), bone and joint pain (MESH:D018771), skeletal deformities (MESH:D009140), abnormal gait (MESH:D020233), loss of physical function (MESH:D059445), muscle pain (MESH:D063806), Fatigue (MESH:D005221), secondary hyperparathyroidism (MESH:D006962), genetic disorder (MESH:D030342), fractures (MESH:D050723), short stature (MESH:D006130), rickets (MESH:D012279), anxiety (MESH:D001007)
- **Chemicals:** EoSG (-), 1,25[OH]2D (MESH:C097949), phosphate (MESH:D010710), Burosumab (MESH:C000601956), vitamin D (MESH:D014807)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13004326/full.md

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Source: https://tomesphere.com/paper/PMC13004326