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Linear Growth and Final Height in Patients with Systemic Juvenile Idiopathic Arthritis Treated with Longterm Glucocorticoids

DOMINIQUE SIMON, CATHERINE FERNANDO, PAUL CZERNICHOW, and ANNE-MARIE PRIEUR

ABSTRACT.

Objective.
To assess linear growth and final height in patients given glucocorticoids during childhood for systemic juvenile idiopathic arthritis (JIA).

Methods. Heights throughout followup for JIA and final height were recorded in 24 patients. Height data were expressed as the height standard deviation score for chronological age (HSDS/CA). Final height was compared to reference values for the French population and to target height.

Results. During glucocorticoid therapy, mean loss of HSDS/CA was -2.7 ± 1.5 and was positively correlated with prednisone therapy duration (p < 0.01). After prednisone discontinuation, 17 patients (70%) had catch-up growth and 7 (30%) continued to experience slow linear growth. Mean final height was -2.0 ± 1.8 HSDS and was correlated with mean height at prednisone discontinuation (p < 0.0001). Mean final height was significantly greater in the patients with catch-up growth at prednisone discontinuation (-1.5 ± 1.6 vs -3.6 ± 1.2 HSDS), and 87% of patients had a final height below their target height.

Conclusion. These data suggest that chronic inflammation and prednisone therapy may adversely affect growth in patients with JIA, and that final height may be closely dependent both on the severity of growth retardation during the active phase of the disease and on linear growth after remission. Thus treatments like growth hormone presently under investigation to improve final height may be most effective when given early after disease onset and/or at remission. (J Rheumatol 2002;29:1296-300)

Key Indexing Terms:

JUVENILE IDIOPATHIC ARTHRITIS
GLUCOCORTICOID THERAPY
GROWTH
GROWTH HORMONE
FINAL HEIGHT


From the Department of Endocrinology and Diabetology, Robert Debré Hospital; and Department of Pediatric Immuno-Hematology and Rheumatology, Necker-Enfants-Malades Hospital, University of Paris V, Paris, France.

D. Simon, MD; C. Fernando, MD; P. Czernichow, MD, Department of Endocrinology and Diabetology, Robert Debré Hospital; A.M. Prieur, MD, Department of Pediatric Immuno-Hematology and Rheumatology, Necker-Enfants-Malades Hospital.

Address reprint requests to Dr. D. Simon, Department of Endocrinology and Diabetology, Hôpital Robert Debré, 48 boulevard Sérurier, 75019 Paris, France.

Submitted May 10, 2001; revision accepted December 7, 2001.




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© 2002. The Journal of Rheumatology Publishing Company Limited.
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