TY - JOUR
T1 - Glucocorticoid-related changes in body mass index among children and adolescents with rheumatic diseases
AU - Shiff, Natalie J.
AU - Brant, Rollin
AU - Guzman, Jaime
AU - Cabral, David A.
AU - Huber, Adam M.
AU - Miettunen, Paivimm
AU - Roth, Johannes
AU - Scuccimarri, Rosie
AU - Alos, Nathalie
AU - Atkinson, Stephanie A.
AU - Collet, Jean Paul
AU - Couch, Robert
AU - Cummings, Elizabeth A.
AU - Dent, Peter B.
AU - Ellsworth, Janet
AU - Hay, John
AU - Houghton, Kristin
AU - Jurencak, Roman
AU - Lang, Bianca
AU - Larche, Maggie
AU - Leblanc, Claire
AU - Rodd, Celia
AU - Saint-Cyr, Claire
AU - Stein, Robert
AU - Stephure, David
AU - Taback, Shayne
AU - Rauch, Frank
AU - Ward, Leanne M.
PY - 2013/1
Y1 - 2013/1
N2 - 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.
AB - 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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U2 - 10.1002/acr.21785
DO - 10.1002/acr.21785
M3 - Article
C2 - 22826190
AN - SCOPUS:84871759333
SN - 2151-464X
VL - 65
SP - 113
EP - 121
JO - Arthritis Care and Research
JF - Arthritis Care and Research
IS - 1
ER -