Evidence map›Paper›PMID 35399930›Full record

Observational studyFrontiers in endocrinology2022

Persistent Lower Limb Deformities Despite Amelioration of Rickets in X-Linked Hypophosphatemia (XLH) - A Prospective Observational Study.

Gabriel T Mindler, Alexandra Stauffer, Andreas Kranzl, Stefan Penzkofer, Rudolf Ganger, Christof Radler, Gabriele Haeusler, Adalbert Raimann

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Real-world impact of treatment on growth in children with X-linked hypophosphatemia.The Journal of clinical endocrinology and metabolism · 2026
    Observational
  2. Article
  3. Lower Limb Deformity in Different Types of Rickets.Journal of clinical medicine · 2025
    Review
  4. Article
  5. Article
  6. UnusualJBMR plus · 2025
    Article
  7. Article
  8. Achondroplasia current concept of orthopaedic management.Journal of children's orthopaedics · 2024
    Review
  9. Article
  10. What's new in pediatric lower limb reconstruction?Journal of children's orthopaedics · 2024
    Article
  11. Impact of burosumab on lower limb alignment in children with X-linked hypophosphatemia.Journal of the Pediatric Orthopaedic Society of North America · 2024
    Article
  12. Article
  13. De Novo Large Deletions in theDiagnostics (Basel, Switzerland) · 2023
    Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Gabriel T MindlerDepartment of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Vienna, Austria.
Alexandra StaufferDepartment of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Vienna, Austria.
Andreas KranzlVienna Bone and Growth Center, Vienna, Austria.
Stefan PenzkoferMRI Institute Bader, Orthopaedic Hospital Speising, Vienna, Austria.
Rudolf GangerDepartment of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Vienna, Austria.
Christof RadlerDepartment of Pediatric Orthopaedics, Orthopaedic Hospital Speising, Vienna, Austria.
Gabriele HaeuslerVienna Bone and Growth Center, Vienna, Austria.
Adalbert RaimannVienna Bone and Growth Center, Vienna, Austria.
Orthopaedic Hospital Speising · ATMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gait deviations, lower limb pain and joint stiffness represent key symptoms in patients with X-linked hypophosphatemia (XLH, OMIM 307800), a rare disorder of mineral homeostasis. While the pathomechanism for rickets is well understood, the direct role of PHEX (Phosphate-regulating neutral endopeptidase) deficiency in non-rachitic features including complex deformities, skull and dental affections remains unclear. FGF23-inhibiting antibody treatment can normalize serum phosphate levels and to improve rickets in XLH patients. However, linear growth remains impaired and effects on lower limb deformity and gait are insufficiently studied. Aims: To characterize and evaluate the course of lower limb deformity in a case series of pediatric XLH patients receiving Burosumab therapy. Methods: Comparative assessment of planar radiographs, gait analysis, biochemical and clinical features of pediatric patients before and ≥12 months after initiation of FGF23-inhibiting was performed prospectively. Lower limb maltorsion was quantified by torsional MRI and gait analysis. Standardized deformity analysis of lower limb anteroposterior radiographs was conducted. Results: Seven patients (age 9.0 +/-3.6 years) were eligible for this study. All patients received conventional treatment before onset of antibody treatment. Maltorsion of the femur was observed in 8/14 legs using torsional MRI (mean antetorsion 8.79°). Maltorsion of the tibia was observed in 9/14 legs (mean external torsion 2.8°). Gait analysis confirmed MRI findings with femoral external malrotation prior to and one year after onset of Burosumab therapy. Internal foot progression (intoeing gait) remained pathological in all cases (mean 2.2°). Knee rotation was pathologically internal 10/14 legs. Mean mechanical axis deviation (MAD) of 16.1mm prior to Burosumab changed in average by 3.9mm. Three children underwent guided growth procedures within the observation period. Mild postprocedural rebound of frontal axis deviation was observed under Burosumab treatment in one patient. Conclusions: This is the first study to investigate lower limb deformity parameters quantitatively in children with XLH receiving Burosumab. One year of Burosumab therapy was associated with persistent maltorsion and frontal axis deviation (varus/valgus) despite improved rickets in this small, prospective uncontrolled study.

Indexed as

Familial Hypophosphatemic RicketsLower ExtremityChildFibroblast Growth FactorsHumansPhosphatesProspective StudiesFibroblast Growth FactorsPhosphatesBurosumabdeformitiesFGF23.phosphateskeletal dysplasiatorsionX-linked hypophosphatemia (XLH)

Identifiers

PMID35399930
PMCPMC8987359
OpenAlexW4220847080

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.