Should adolescents with glomerulopathies be treated as children or adults?

Should adolescents with glomerulopathies be treated as children or adults?

Author Requiao-Moura, Lucio R. Autor UNIFESP Google Scholar
Freitas, Taina Veras de S. Autor UNIFESP Google Scholar
Franco, Marcello F. Autor UNIFESP Google Scholar
Pereira, Aparecido B. Autor UNIFESP Google Scholar
Mastroianni-Kirsztajn, Gianna Autor UNIFESP Google Scholar
Institution Universidade Federal de São Paulo (UNIFESP)
Abstract Background: Glomerular diseases are an important cause of end-stage renal disease, especially among young adults. However, clinical and epidemiological surveys involving adolescent populations are scarce. Aim: To determine the pattern of glomerulopathies (GP) in adolescents submitted to renal biopsy.Methods: A retrospective study of patients' records of the Glomerulopathy Section, UNIFESP (Brazil), was performed.Results: Among 72 adolescents (12-18 years) with GP, 15.6 +/- 1.5 years, 58.3% females, the most frequent clinical manifestation was nephrotic syndrome (NS, 71%) and focal segmental glomerulosclerosis (FSGS) was the main histological pattern (24%), followed by minimal change disease (MCD, 19.5%). After comparing the main causes of NS in adolescents with those of adults, we found no statistically significant differences in clinical presentation or outcome. Renal failure-free survival of 1 and 5 years for all GP corresponded to 87.9 and 73.6%, respectively (88.5 and 76.3% for NS).Conclusions: NS was the main manifestation; FSGS and MCD were the most common histological diagnoses. Our data suggest the GP and particularly the NS pattern in adolescents is similar to that of adults, pointing to the need for an adaptation in diagnostic and treatment protocols for this age group, a pattern which corresponds more closely to that of adults. Copyright (c) 2008 S. Karger AG, Basel.
Keywords adolescent
glomerular disease
nephrotic syndrome
Language English
Date 2008-01-01
Published in Nephron Clinical Practice. Basel: Karger, v. 109, n. 3, p. C161-C167, 2008.
ISSN 1660-2110 (Sherpa/Romeo, impact factor)
Publisher Karger
Extent C161-C167
Access rights Closed access
Type Article
Web of Science ID WOS:000258726000008

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