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Glucocorticoid-related changes in body mass index among children and adolescents with rheumatic diseases
Natalie J Shiff1, Rollin Brant, Jaime Guzman
1University of Saskatchewan, Saskatoon, Saskatchewan, Canada. natalie.shiff@usask.ca
Insights
Glucocorticoids (GCs) significantly impact children's body mass index (BMI) in rheumatic diseases. High-dose GCs led to a peak BMI Z score at 4 months, with only half of children returning to baseline after 18 months.
Area of Science:
- Pediatric Rheumatology
- Endocrinology
- Growth and Development
Background:
- Glucocorticoids (GCs) are essential for managing pediatric rheumatic diseases.
- GC therapy can lead to significant side effects, including metabolic changes.
- Understanding the impact of GCs on body mass index (BMI) is crucial for long-term patient health.
Purpose of the Study:
- To investigate the temporal and dose-dependent effects of GCs on BMI in children with rheumatic conditions.
- To identify factors influencing BMI changes during GC treatment.
Main Methods:
- Longitudinal study of 130 children initiating GCs for rheumatic disease over 18 months.
- Assessment of BMI, weight, and height Z scores based on GC dosage (high, moderate, low).
- Mixed-effects growth curve models analyzed the impact of GC dose, diagnosis, puberty, activity, and disease activity on BMI and body fat.
Main Results:
- High-dose GCs (≥1.0 mg/kg/day) resulted in a peak BMI Z score of +1.29 at 4 months.
- Moderate-dose GCs (<0.2 mg/kg/day to 7.5 mg/day) showed a peak BMI Z score of +0.69 at 4.2 months.
- GC dose was the primary determinant of BMI Z score and body fat; disease activity and diagnosis also played a role.
Conclusions:
- Children with rheumatic diseases on moderate to high-dose GCs experience a peak in BMI Z scores around 4 months.
- Approximately 50% of children did not return to their baseline BMI Z score within 18 months of GC initiation.
- GC therapy necessitates careful monitoring of BMI and metabolic health in pediatric patients.
Objective:
To examine the temporal and dose-related effects of glucocorticoids (GCs) on body mass index (BMI) in children with rheumatic diseases.
Methods:
Children initiating GCs for a rheumatic disease (n = 130) were assessed every 3 months for 18 months. BMI, weight, and height Z score trajectories were described according to GC starting dosage in prednisone equivalents: high (≥1.0 mg/kg/day), low (<0.2 mg/kg/day to a maximum of 7.5 mg/day), and moderate (between high and low) dosage. The impact of GC dosing, underlying diagnosis, pubertal status, physical activity, and disease activity on BMI Z scores and on percent body fat was assessed with longitudinal mixed-effects growth curve models.
Results:
The GC starting dose was high in 59% and moderate in 39% of patients. The peak BMI Z score was +1.29 at 4 months with high-dose GCs and +0.69 at 4.2 months with moderate-dose GCs (P < 0.001). Overall, 50% (95% confidence interval 41-59%) of the children returned to within +0.25 SD of their baseline BMI Z score. Oral GC dose over the preceding 3 months was the most significant determinant of BMI Z score and percent body fat. The proportion of days in receipt of GCs, disease activity, and a diagnosis of systemic-onset juvenile idiopathic arthritis were also associated with BMI Z scores. The correlation between changes in BMI and changes in percent body fat was 0.09.
Conclusion:
In children with rheumatic diseases starting moderate and high doses of GCs, BMI Z scores peaked at 4 months, and only half returned to within +0.25 SD of their baseline BMI Z score after 18 months.
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