Bone mineral density in children with cirrhosis
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Updated: Jul 19, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Nuray Uslu1, Inci Nur Saltik-Temizel, Hülya Demir
1Hacettepe University, Faculty of Medicine, Department of Pediatrics, Section of Gastroenterology, Hepatology and Nutrition, Ankara 06100, Turkey.
Insights
Children with cirrhosis have significantly lower bone mineral density and content compared to healthy children. Early evaluation for osteopenia is recommended for pediatric cirrhosis patients.
Area of Science:
- Pediatric Endocrinology
- Hepatology
- Bone Metabolism
Background:
- Osteoporosis is a significant concern in adults with cirrhosis, but data on pediatric populations are limited.
- This study addresses the knowledge gap regarding bone health in children suffering from cirrhosis.
Purpose of the Study:
- To evaluate and compare bone mineral density (BMD) and bone mineral content (BMC) in children with cirrhosis versus healthy controls.
- To determine if children with cirrhosis exhibit reduced bone mass.
Main Methods:
- Dual-energy X-ray absorptiometry (DXA) was used to measure lumbar spine BMD and BMC in 40 children with cirrhosis (mean age 10.4 years).
- Results were compared to 62 age- and sex-matched healthy children.
- Statistical analysis controlled for confounding factors like weight, height, and pubertal stage.
Main Results:
- Children with cirrhosis showed significantly lower mean lumbar spine BMD (0.482 g/cm²) compared to healthy controls (0.687 g/cm²; P < 0.0001).
- Mean lumbar spine BMC was also significantly reduced in children with cirrhosis (20.008 g) versus controls (32.859 g; P < 0.0001).
- These differences remained significant after adjusting for weight, height, and pubertal stage.
Conclusions:
- Pediatric patients with cirrhosis exhibit significantly diminished bone mineral density and content.
- These findings underscore the need for routine bone health assessment in children diagnosed with cirrhosis.
- Early detection and management of osteopenia are crucial for this vulnerable pediatric group.
Background:
Despite the clinical importance of osteoporosis in individuals with cirrhosis, little is known about it, especially in children. We evaluated the bone mineral density (BMD) and bone mineral content (BMC) of children with cirrhosis.
Methods:
Forty children with cirrhosis (mean age, 10.4 +/- 3.9 years) were involved. BMD and BMC were measured by dual energy X-ray absorptiometry at lumbar vertebrae 1-4, and the results were compared with those of 62 healthy age- and sex-matched children.
Results:
The mean lumbar spine BMD of patients with cirrhosis was 0.482 +/- 0.107 g/cm(2) and that of the controls was 0.687 +/- 0.172 g/cm(2) (P < 0.0001). The mean lumbar spine BMC of patients with cirrhosis was 20.008 +/- 8.409 g and that of controls was 32.859 +/- 14.665 g (P < 0.0001). After the confounding variables (weight, height, and pubertal stage) were controlled for, the difference in BMD and BMC values between patients with cirrhosis and healthy controls was significant (0.535 +/- 0.061 g/cm(2) vs 0.653 +/- 0.048 g/cm(2), and 24.515 +/- 5.052 g vs 29.952 +/- 3.971 g, respectively).
Conclusions:
Because of the significant difference in BMD and BMC values between our patients with cirrhosis and healthy controls, patients with cirrhosis should be evaluated for osteopenia.
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