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Updated: Jul 14, 2026

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma
Published on: November 4, 2010
[Inhaled corticosteroid therapy and bone metabolism in asthmatic children]
C Galván Fernández1, C Oliva Hernández, R S Suárez López de Vergara
1Centros de Salud Laguna-S Benito y Finca, Spain. cgalvanf@comtf.es
Insights
Inhaled corticosteroids (ICS) therapy in children with asthma may impact bone mineral density (BMD), potentially increasing osteopenia risk. Bone formation and resorption markers remain unaffected by ICS treatment.
Area of Science:
- Pediatric Endocrinology
- Respiratory Medicine
- Bone Metabolism
Context:
- Asthma is a common chronic respiratory disease in children.
- Inhaled corticosteroids (ICS) are the mainstay of asthma treatment.
- Potential long-term effects of ICS on bone metabolism require investigation.
Purpose:
- To investigate the association between ICS therapy and bone metabolism in children.
- To compare bone mineral density (BMD) and bone turnover markers in asthmatic children on ICS with healthy children.
Summary:
- 151 children (1-17 years) were studied: 71 on long-term ICS, 44 on intermittent ICS, and 36 healthy controls.
- Significant differences in BMD were observed between long-term ICS users and healthy controls.
- No significant differences in bone formation or resorption markers were found among the groups.
Impact:
- ICS treatment in asthmatic children may negatively affect BMD, increasing osteopenia risk.
- Osteopenia in these children might be influenced by factors beyond ICS therapy.
- Further research is needed to elucidate the multifactorial nature of bone metabolism changes in pediatric asthma.
Objective:
To explore the association between inhaled corticosteroids (ICS) therapy and bone metabolism.
Patients And Methods:
The sample was composed of 151 children, aged between 1 and 17 years. There were 71 asthmatics treated with ICS for at least 6 months (group 1), 44 asthmatics treated occasionally with ICS during exacerbations (group 2), and 36 healthy children (group 3). Bone mineral density (BMD) and markers of bone formation and resorption were measured. These measures, as well as other related factors, were compared among groups. Regression models for osteopenia and BMD were used with the group as the independent variable adjusted by factors with differences between groups. A two-tailed level of p < 0.05 was used in all tests.
Results:
No differences in BMD were found between groups 1 and 2 but significant differences were found between groups 1 and 3 (p = 0.003). No differences were found in markers of bone formation and resorption among the groups. No association was found between BMD and the type, daily dose or accumulated dose of ICS. Group 1 showed an osteopenia odds ratio relative to group 3 of 2.94 (95 % CI: 1.49-5.78) and an average reduction of BMD of 0.50 (95 % CI: 0.32-0.68) was found from group 3 to 2 and from group 2 to 1. In group 1, markers of bone resorption significantly increased in asthmatics with osteopenia compared with those without osteopenia.
Conclusions:
ICS treatment in asthmatic children seems to affect BMD. Markers of bone formation and resorption are unaffected. Osteopenia in these children could also be related to other factors that increase bone resorption.
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