Evidence map›Paper›PMID 42850326›Full record

Observational studyEuropean journal of pediatrics2026

Vitamin D status and adiposity in children with low-energy fractures: a prospective case-control study.

Andrea Cosentino, Daniel Weghuber, Pier Francesco Indelli, Nicole Fantini, Wilhelm Berger, Olaf Stefan Schmidt, Wolfgang Högler

Registry-linked trialAbstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07143552 (A Prospective Case-Control Study of Vitamin D Status, Bone Metabolic Markers, and Overweight in Pediatric Low-Energy Fractures), which is not on this map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

NCT07143552 recruitingnot on this map

A Prospective Case-Control Study of Vitamin D Status, Bone Metabolic Markers, and Overweight in Pediatric Low-Energy Fractures

TypeobservationalSponsorParacelsus Medical UniversityRan2024 to 2026Enrolled100ConditionsPediatric Fractures, Hypovitaminosis D, Obesity and Overweight
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Andrea CosentinoParacelsus Medical University, Strubergasse 21, 5020, Salzburg, Austria. andreacosentino2@gmail.com.ORCID http://orcid.org/0000-0001-7885-512X
Daniel WeghuberDepartment of Pediatrics, Paracelsus Medical University, Strubergasse 21, 5020, Salzburg, Austria.
Pier Francesco IndelliInstitute of Biomechanics, Paracelsus Medical University, Strubergasse 21, 5020, Salzburg, Austria.
Nicole FantiniDepartment of Pediatrics, Hospital of Merano (SABES-ASDAA), Via Rossini 5, 39012, Merano-Meran, Italy.
Wilhelm BergerDepartment of Orthopedics and Traumatology, Hospital of Merano (SABES-ASDAA), Via Rossini 5, 39012, Merano-Meran, Italy.
Olaf Stefan SchmidtDepartment of Orthopedics and Traumatology, Hospital of Merano (SABES-ASDAA), Via Rossini 5, 39012, Merano-Meran, Italy.
Wolfgang HöglerCentre for Growth and Osteology, Department of Paediatrics and Adolescent Medicine, Johannes Kepler University, 4020, Linz, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fractures in children are influenced by both skeletal biology and mechanical factors. While alterations in vitamin D and other metabolic markers have been proposed as contributors to fracture risk, their role in predicting fractures in otherwise healthy pediatric populations remains unclear. This study aimed to determine whether biochemical markers of bone metabolism and body mass are independently associated with fracture occurrence and fracture patterns in children after low-energy trauma and to assess their impact on fracture patterns and anatomical distribution. We conducted a prospective case-control study including 100 children presenting after low-energy trauma (50 with radiographically confirmed fractures and 50 controls). Serum 25OH vitamin D (25OHD), parathyroid hormone (PTH), calcium, phosphate, and alkaline phosphatase (ALP) were measured within 1 week of presentation. Associations with fracture occurrence were assessed using multivariable logistic regression, including age, sex, body mass index z-score (BMI-z), an interaction term between 25OHD and BMI-z, and an additional exploratory model evaluating a 25OHD × season interaction. The discriminatory ability of 25OHD was evaluated using receiver operating characteristic analysis. Children with fractures had lower serum 25OHD concentrations and a higher prevalence of levels below 50 nmol/L compared with controls. Other biochemical markers were largely within normal ranges, although ALP levels were modestly higher in fracture patients. In multivariable analysis, 25OHD levels below 50 nmol/L were associated with increased odds of fracture, whereas age and BMI-z were not independently associated with fracture occurrence. However, a significant interaction between 25OHD and BMI-z was observed, indicating that the association between vitamin D status and fracture risk is influenced by adiposity. The overall discriminatory ability of 25OHD for fracture risk was modest.

conclusionLower 25OHD levels were observed in children with low-energy fractures. The association between vitamin D status and fracture risk appears to be modest and influenced by adiposity, with a more pronounced effect at higher BMI-z levels. Therefore, fracture susceptibility in otherwise healthy children is likely driven primarily by biomechanical and developmental factors rather than vitamin D status, supporting a targeted rather than routine laboratory assessment of metabolic markers in children presenting with fractures. CLINICALTRIALS: gov Identifier: NCT07143552. WHAT IS KNOWN: • Lower serum 25-hydroxyvitamin D concentrations have been reported in children with fractures, but the relationship between vitamin D status and fracture risk remains controversial. • Childhood obesity is associated with lower circulating vitamin D concentrations and may independently influence fracture susceptibility. WHAT IS NEW: • Vitamin D insufficiency (< 50 nmol/L) was associated with increased odds of low-energy fractures in children, although its overall discriminatory ability was modest. • The association between vitamin D status and fracture risk was modified by adiposity, with a stronger relationship observed in children with higher BMI-z. • Biochemical markers of bone mineralization were largely normal, supporting the concept that fracture susceptibility in otherwise healthy children is driven predominantly by biomechanical and developmental factors rather than clinically relevant metabolic bone disease.

Indexed as

AdiposityFractures, BoneVitamin DVitamin D DeficiencyAdolescentAlkaline PhosphataseBiomarkersBody Mass IndexCase-Control StudiesChildChild, PreschoolFemaleHumansLogistic ModelsMaleParathyroid Hormone25-hydroxyvitamin DAlkaline PhosphataseBiomarkersParathyroid HormoneVitamin DAdiposityAlkaline phosphataseBody mass indexBone mineralizationCalcium metabolismLow-energy traumaParathyroid hormonePediatric bone healthPediatric fractureVitamin D

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Registered trials

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.