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Published on: January 29, 2018
Patterns of bone mineral acquisition in children with epidermolysis bullosa: a longitudinal study
1Department of Dermatology Pediatrics, Stanford University School of Medicine, Stanford, CA 94305-5168, USA.
Insights
Children with generalized epidermolysis bullosa (EB) show inadequate bone mineral density (BMD) gains, not premature bone loss. Interventions are needed to improve bone health in these patients.
Area of Science:
- Pediatric Endocrinology
- Bone Metabolism
- Genetic Disorders
Background:
- Generalized epidermolysis bullosa (EB) is associated with reduced bone mass and fractures.
- The underlying cause of bone density issues in EB, whether poor acquisition or accelerated loss, remains unclear.
Purpose of the Study:
- To investigate bone mineral acquisition patterns in children with generalized EB.
- To identify clinical and laboratory factors associated with changes in areal bone mineral density (aBMD) over time.
Main Methods:
- A longitudinal study of 17 children (≥6 years) with generalized EB over at least 12 months.
- Evaluations included clinical assessments, laboratory tests, and dual-energy X-ray absorptiometry (DXA) of the lumbar spine.
- Statistical analyses compared baseline and follow-up measures and group differences based on aBMD Z-score changes.
Main Results:
- While subjects grew in height and weight, mean Z-scores for these parameters did not significantly improve.
- Lumbar spine bone mineral content and aBMD increased significantly, but mean aBMD Z-scores remained unchanged.
- No significant differences in clinical or laboratory characteristics were found between subjects who gained aBMD Z-scores and those who did not.
Conclusions:
- Inadequate bone mineral density accrual, rather than bone loss, is the primary driver of low bone mass in children with generalized EB.
- Clinical interventions targeting overall health and bone building are recommended for this population.
Background:
Reduced bone mass and fractures are known complications of generalized forms of epidermolysis bullosa (EB). However, the aetiology - inadequate bone acquisition, premature bone loss, or a combination - is unclear.
Objectives:
To determine patterns of bone mineral acquisition in children with EB and to identify clinical and laboratory correlates of change in areal bone mineral density (aBMD).
Methods:
Seventeen subjects ≥ 6 years of age with generalized EB were studied at two visits at least 12 months apart with clinical and laboratory evaluations and dual energy X-ray absorptiometry scans of the lumbar spine. Wilcoxon signed-rank tests were used to determine if changes from baseline to follow-up were significant. Wilcoxon rank-sum tests were used to compare subjects with gains in aBMD Z-score with those who experienced no change or decreases to determine if baseline laboratory or clinical characteristics differed between the two groups.
Results:
Subjects gained height and weight at follow-up, but there was no significant improvement in mean Z-scores for height, weight or body mass index. Laboratory values did not change significantly. Mean bone mineral content and aBMD of the lumbar spine increased significantly at follow-up, but mean aBMD Z-scores remained static. No differences in clinical characteristics or laboratory values were seen between subjects with increased aBMD Z-scores vs. those whose scores decreased or did not change.
Conclusions:
Low bone mass in children with generalized EB is due primarily to inadequate gains in aBMD. Interventions to improve overall health and to help build bone mass in this patient population are warranted.
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