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Updated: Jun 18, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Bone mineral and body composition alterations in paediatric cystic fibrosis patients
Philippe Reix1, Gabriel Bellon, Pierre Braillon
1Service de Pédiatrie, Pneumologie, Allergologie, Mucoviscidose, Hôpital Femme Mère Enfant, 59 boulevard Pinel, Bron cedex, France. philippe.reix@chu-lyon.fr
Insights
Children with cystic fibrosis (CF) show early bone density issues, with body composition changes varying by age. Monitoring bone mineral status using dual-energy X-ray absorptiometry (DXA) is effective in this population.
Area of Science:
- Pediatric Endocrinology
- Bone Metabolism
- Body Composition Analysis
Background:
- Increasing lifespan in cystic fibrosis (CF) patients raises concerns about CF-related bone diseases.
- Previous studies on bone mineralization in children with CF have produced conflicting results.
Purpose of the Study:
- To monitor body composition and bone mineral status in children with CF.
- To assess the utility of dual-energy X-ray absorptiometry (DXA) for evaluating bone health in pediatric CF patients.
Main Methods:
- Review of DXA data from 161 children with CF (mean age 10 years).
- Measurement of total body bone mineral content (BMCt), lean tissue mass (LTMt), and fat mass (FMt).
- Comparison of measured values to ideal weight-for-height standards using BMCt/BMCti, LTMt/LTMti, and FMt/FMti ratios (bt, lt, ft).
Main Results:
- A low bone mineral content ratio (bt) was observed across all age groups (mean bt ratio 0.94).
- Lean tissue mass ratio (lt) decreased in children under 10, while fat mass ratio (ft) increased with age.
- Poor clinical status, nutritional status, and vitamin A levels correlated with lower bt and lt ratios.
Conclusions:
- Children with CF may experience early alterations in bone status.
- Body composition ratios (lt and ft) vary with age in children with CF.
- DXA analysis using standardized ratios is a suitable method for monitoring CF-related bone disease in children.
Background:
With the increased life span of cystic fibrosis (CF) patients, CF-related bone diseases could have an increased prevalence and morbidity in this group. In children, previous retrospective and prospective studies have yielded conflicting results on bone mineralization.
Objective:
To monitor body composition and bone mineral status of children with CF.
Materials And Methods:
We reviewed the dual-energy X-ray absorptiometry (DXA) data of 161 children with CF (age 10 +/- 4.8 years). Total body bone mineral content (BMCt), total lean tissue mass (LTMt) and total fat mass (FMt) were measured and compared to expected data calculated from ideal weight for height (Wi; e.g. BMCti, LTMti, FMti). The bt (BMCt/BMCti), lt (LTMt/LTMti) and ft (FMt/FMti) ratios were used as quantitative variables.
Results:
Low bt ratio was found at all ages (mean bt ratio 0.94 +/- 0.10; P < 0.001), even in children <6 years of age. However, the children's BMCt was satisfactorily adapted to their weight. lt and ft ratios were not constant across age groups. Children <10 years had 8% reduction of their lt ratio, maintaining normal levels thereafter. The opposite trend was found for ft ratio. Poor clinical, nutritional status and vitamin A levels were correlated with bt and lt ratios.
Conclusion:
Our results indicate that children with CF could have early alterations in their bone status and that lt and ft ratios did not have constant values across ages. Interpreting DXA data using this approach is suitable in children with CF.
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