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Updated: Jun 5, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Bone assessment in children with chronic kidney disease: data from two new bone imaging techniques in a single-center
Justine Bacchetta1, Stéphanie Boutroy, Nicolas Vilayphiou
1Service de Néphrologie et Rhumatologie Pédiatriques, Centre de Référence des Maladies Rénales Rares, Hôpital Femme Mère Enfant, 59 Bd Pinel, 69677, Bron, France. justine.bacchetta@chu-lyon.fr
Insights
Pediatric chronic kidney disease (CKD) patients showed no significant bone microarchitecture differences compared to controls using advanced imaging. Further longitudinal studies are needed to understand bone health in pediatric CKD.
Area of Science:
- Pediatric Nephrology
- Bone Metabolism
- Medical Imaging
Background:
- Bone damage is a significant challenge in pediatric chronic kidney disease (CKD).
- Dual-energy X-ray absorptiometry (DXA) for bone mineral density (BMD) assessment has limitations in CKD patients.
- Novel imaging techniques are needed to better evaluate bone quality in children with CKD.
Purpose of the Study:
- To evaluate bone quality in children with CKD using advanced imaging techniques.
- To compare bone microarchitecture and volumetric BMD between CKD children and healthy controls.
- To explore bone texture analysis in younger CKD patients.
Main Methods:
- Pilot cross-sectional study involving 22 CKD children and 19 healthy controls.
- High-resolution peripheral quantitative computed tomography (HR-pQCT) for bone imaging and microarchitecture assessment.
- Bone texture analysis (BMA) performed on younger patients and controls.
Main Results:
- Older CKD children had lower height and weight but comparable BMD and microarchitecture to controls.
- Cortical BMD correlated significantly with glomerular filtration rate, age, and BMI in univariate analysis.
- No significant differences in bone texture parameters were found between younger CKD patients and controls.
Conclusions:
- Current advanced bone imaging techniques appear feasible for pediatric CKD assessment.
- No significant differences in bone density or microarchitecture were detected between CKD children and controls in this pilot study.
- Further longitudinal research is essential to investigate the long-term bone and cardiovascular effects of CKD-related metabolic dysregulation.
Abstract:
Bone damage in children with chronic kidney disease (CKD) is a challenge for pediatric nephrologists. Areal measurements of bone mineral density (BMD) by dual x-ray absorptiometry (DXA) have been routinely performed to assess bone mass but recent international guidelines have concluded that DXA was of less value in CKD. The aim of this study is to evaluate bone quality in CKD children using new bone imaging techniques in a pilot cross-sectional single-center study. We performed bone imaging (high-resolution peripheral quantitative computed tomography, HR-pQCT, XtremeCT, Scanco Medical AG, Switzerland), to assess compartmental volumetric BMD and trabecular microarchitecture in 22 CKD children and 19 controls. In seven younger patients (i.e., under 10 years of age), we performed bone texture analysis (BMA, D3A Medical Systems, France) in comparison to 15 healthy prepubertal controls. Among older children, CKD patients had significantly lower height and body weight without significant impairment of BMD and microarchitecture than healthy controls. In univariate analysis, there were significant correlations between cortical BMD and glomerular filtration rate (r= -0.46), age (r=0.60) and body mass index (r=0.67). In younger children, bone texture parameters were not different between patients and controls. Our results did not show significant differences between healthy controls and CKD children for compartmental bone densities and microarchitecture, but the small sample size and the heterogeneity of the CKD group require caution in the interpretation. Novel bone imaging techniques seem feasible in children, and further longitudinal studies are required to thoroughly explore long-term cardiovascular and bone consequences of phosphate-calcium metabolism deregulation during CKD.
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