Steroid-sensitive nephrotic syndrome: From childhood to adulthood

Background: The clinical presentation, treatment, and outcome of steroid-sensitive nephrotic syndrome (SSNS) during childhood have been extensively studied. Conversely, few data regarding the outcome in adulthood of childhood SSNS have been published previously. We undertook to conduct a retrospecti...

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Published in:American journal of kidney diseases Vol. 41; no. 3; pp. 550 - 557
Main Authors: Fakhouri, Fadi, Bocquet, Nathalie, Taupin, Pierre, Presne, Claire, Gagnadoux, Marie-France, Landais, Paul, Lesavre, Philippe, Chauveau, Dominique, Knebelmann, Bertrand, Broyer, Michel, Grünfeld, Jean-Pierre, Niaudet, Patrick
Format: Journal Article
Language:English
Published: Orlando, FL Elsevier Inc 01-03-2003
Elsevier
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Summary:Background: The clinical presentation, treatment, and outcome of steroid-sensitive nephrotic syndrome (SSNS) during childhood have been extensively studied. Conversely, few data regarding the outcome in adulthood of childhood SSNS have been published previously. We undertook to conduct a retrospective study of the outcome in adulthood of a large cohort of patients diagnosed with an SSNS during childhood. Methods: We identified all children born between 1970 and 1975 who had been admitted to our institution for an SSNS. Data regarding the outcome in adulthood of these patients were obtained through mailed questionnaires or phone calls to patients and/or their parents or through attending physicians. Results: One hundred seventeen patients were identified. Data regarding the outcome of SSNS in adulthood were available for 102 patients (87.2%). Forty-three patients (42.2%) experienced at least one relapse of nephrotic syndrome in adulthood. By univariate analysis, young age at onset (<6 years) and more severe disease in childhood, indicated by a greater number of relapses (12.9 for adulthood relapsers versus 5.4 for adulthood nonrelapsers; P < 0.0001) and more frequent use of immunosuppressors (74.4% versus 31.6%; P < 0.0001) or cyclosporine (42.9% versus 7.3%; P < 0.0001) were predictive of the occurrence of SSNS relapse in adulthood. Conversely, relapse rate in the first 6 months of disease was not predictive of further relapses in adulthood. By multivariate analysis, only number of relapses during childhood was predictive of adulthood relapses (P < 0.0058). Long-term side effects of steroids were found in 44.2% of adulthood relapsers; the most frequent were osteoporosis and excess weight. Conclusion: The incidence of childhood SSNS relapses in adulthood was relatively high in our study. Further studies are required to assess long-term complications in adults with relapses and a history of prolonged steroid and immunosuppressor use. Am J Kidney Dis 41:550-557. © 2003 by the National Kidney Foundation, Inc.
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ISSN:0272-6386
1523-6838
DOI:10.1053/ajkd.2003.50116