Evidence map›Paper›PMID 40493262›Full record

Observational studyPediatric nephrology (Berlin, Germany)2025

Growth dynamics of transversal body dimensions and proportions, with related clinical determinants in children with X-linked hypophosphatemia treated with phosphate supplements and active vitamin D.

Laura Celine Brieger, Stephan Przygodda, Alina Verena Bohlen, Mirko Rehberg, Martin Konrad, Karl Peter Schlingmann, Olaf Hiort, Dorothee Schmidt, Ulrike John-Kroegel, Elke Wuehl and 35 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Pediatric nephrology (Berlin, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Observational
  2. Real-world impact of treatment on growth in children with X-linked hypophosphatemia.The Journal of clinical endocrinology and metabolism · 2026
    Observational
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

45 authors.

Laura Celine BriegerDepartment of Pediatric Kidney, Liver and Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Stephan PrzygoddaDepartment of Pediatric Kidney, Liver and Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Alina Verena BohlenDepartment of Pediatric Kidney, Liver and Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Mirko RehbergDepartment of Pediatrics, Faculty of Medicineand, University Hospital Cologne, University of Cologne, Cologne, Germany.
Martin KonradDepartment of General Pediatrics, Pediatric Nephrology, University Children's Hospital, Münster, Germany.
Karl Peter SchlingmannDepartment of General Pediatrics, Pediatric Nephrology, University Children's Hospital, Münster, Germany.
Olaf HiortDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University of Lübeck, Lübeck, Germany.
Dorothee SchmidtDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University of Lübeck, Lübeck, Germany.
Ulrike John-KroegelDepartment of Pediatric Nephrology, University Children's Hospital, Jena, Germany.
Elke WuehlCenter for Pediatric and Adolescent Medicine, Division of Pediatric Nephrology, Heidelberg University, Heidelberg, Germany.
Markus Josef KemperAsklepios Children's Hospital Hamburg-Heidberg, Hamburg, Germany.
Ute DerichsUniversity Children's Hospital, Mainz, Germany.
Ludwig PatzerElisabeth and St, Barbara Children's Hospital, Halle/Saale, Germany.
Norbert AlbersChristliches Kinderhospital Osnabrück, Osnabrück, Germany.
Desiree DunstheimerDepartment of Paediatric Endocrinologyand, Diabetology University Hospital of Augsburg, Augsburg, Germany.
Sabine HegerKinderkrankenhaus Auf Der Bult, Hannover, Germany.
Karina Grohmann-HeldUniversity Children's Hospital Greifswald, Greifswald, Germany.
Carmen SchroederUniversity Children's Hospital Greifswald, Greifswald, Germany.
Norbert JorchUniversity Children's Hospital, Evangelisches Klinikum Bethel, Bielefeld, Germany.
Elmar SchmidClinic for Pediatric Nephrology Hirschaid, Hirschaid, Germany.
Hagen StaudeUniversity Children's Hospital Rostock, Rostock, Germany.
Marcus WeitzDepartment of General Pediatrics and Hematology/Oncology, University Children's Hospital Tübingen, Tübingen, Germany.
Clemens FreibergDepartment of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, Göttingen, Germany.
Angela HuebnerDepartment of Pediatrics, Faculty of Medicineand, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Anke Heitmeyer-PyperDiessen Am Ammersee, Ammersee Ärzte Diessen, Ammersee, Germany.
Giuseppina SpartaDivision of Pediatric Nephrology, University Children's Hospital Zurich, Zurich, Switzerland.
Carl-Joachim PartschCenter for Hormonal and Metabolic Diseases, Reproductive Medicine and Prenatal Medicine, Endokrinologikum Hamburg, Hamburg, Germany.
Michaela MarxPediatric Endocrinology, Children's Hospital Erlangen, Erlangen, Germany.
Christof LandChild and Adolescent Medicine, Gauting, Germany.
Inka BausUniversity MVZ Kiel, Schleswig-Holstein University Hospital, Kiel, Germany.
Frauke WilkeningHelios Children's Hospital Schwerin, Schwerin, Germany.
Kristina MoellerDepartment of Pediatrics and Adolescent Medicine, Eltern-Kind-Zentrum Prof. Hess, Klinikum Bremen Mitte, Pediatric Nephrology, Bremen, Germany.
Gunter Simic-SchleicherKlinikum Bremen-Nord, Bremen, Germany.
Susann EmptingDepartment of Paediatric Endocrinology and Diabetology, University Children's Hospital Magdeburg, Magdeburg, Germany.
Oliver MetzingDepartment of Pediatric Endocrinology, University Children's Hospital, Jena, Germany.
Verena WagnerPediatric Practice Rostock - Endocrinology and Diabetology, Rostock, Germany.
Martin HolderPediatric Diabetology and Endocrinology, Klinikum Stuttgart, Children's Hospital, OlgahospitalStuttgart, Germany.
Mislav Stjepan ŽebecInstitute for Anthropological Research, Zagreb, Croatia.
Dirk SchnabelCenter for Chronically Sick Children, Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Dieter HaffnerDepartment of Pediatric Kidney, Liver and Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Miroslav ZivicnjakDepartment of Pediatric Kidney, Liver and Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany. zivicnjak.miroslav@mh-hannover.de.ORCID http://orcid.org/0000-0001-9302-712X
on behalf of
German Society for Pediatric Nephrology (GPN)
German Society for Pediatric
Adolescent Endocrinology, Diabetology (DGKED)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildren with X-linked hypophosphatemia (XLH) present with rickets, leg deformities, and growth failure. Bone stability depends on balanced bone growth in both length and width. Data on body proportions, including transverse body dimensions, in children with XLH treated with phosphate supplements and active vitamin D are lacking.

methodsSix major transverse body dimensions of the trunk and extremities, and the frame index (FI), i.e., ratio between bicondylar humerus diameter and height, were measured annually along with clinical characteristics in 109 pediatric patients with XLH, all on supplementation therapy, participating in a prospective multicenter observational study conducted since 1998. Associations between anthropometric and clinical parameters were investigated using linear mixed-effects models.

resultsChildren with XLH exhibited persistent hypophosphatemia and elevated alkaline phosphatase z scores despite supplementation treatment. This was associated with disproportionate transversal skeletal growth, which was most pronounced during adolescence (13-17 years). Bicondylar diameter z scores (tubular bone width) and FI progressively increased with age (each p < 0.05). In addition, FI was identified as a superior indicator of stunting when compared to other measures of transversal dimensionality across all age groups. In young children (2-6 years), transversal growth was most synchronized and associated most strongly with clinical characteristics.

conclusionsOur data show disproportionate growth in transversal body dimensions despite supplementation treatment in children with XLH, suggesting compensatory widening of tubular bones as adaptation for mineral loss caused by persisting rickets. The FI can be used as a general indicator of bone health in children with XLH in clinical practice and trials.

Indexed as

Bone DevelopmentFamilial Hypophosphatemic RicketsPhosphatesVitamin DAdolescentChildChild, PreschoolDietary SupplementsFemaleHumansMaleProspective StudiesPhosphatesVitamin DAlkaline phosphataseBody disproportionFrame indexPhosphateRicketsTransversal body dimensionXLH

Identifiers

PMID40493262
PMCPMC12401769

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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.