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Published in: Pediatric Nephrology 1/2014

01-01-2014 | Original Article

Do C1q or IgM nephropathies predict disease severity in children with minimal change nephrotic syndrome?

Authors: Mateja Vintar Spreitzer, Alenka Vizjak, Dušan Ferluga, Rajko B. Kenda, Tanja Kersnik Levart

Published in: Pediatric Nephrology | Issue 1/2014

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Abstract

Background

It has been suggested that C1q and immunoglobulin M (IgM) nephropathy are variants of minimal change nephrotic syndrome (MCNS). Many researchers believe that these two conditions signify a worse prognosis for children with MCNS in comparison with immunofluorescence (IF)-negative MCNS. The aim of our study was to determine the prognostic significance of C1q nephropathy and IgM nephropathy in children with MCNS.

Methods

Fifty-five children with MCNS who had been biopsied over the course of 24 years at our institution were retrospectively categorized into three groups on the basis of IF microscopy findings: IF-negative MCNS (29/55 patients), MCNS with IgM nephropathy (19/55 patients), and MCNS with C1q nephropathy (7/55 patients). Clinical characteristics at disease presentation, clinical course, and renal outcome were compared between groups during the median follow-up period of 16.9 years (minimum 1.0, maximum 31.1 years).

Results

No statistically significant differences in clinical characteristics at disease presentation, clinical course, and renal outcome were found. Children with IgM nephropathy, C1q nephropathy, and IF-negative MCNS were clinically indistinguishable.

Conclusions

We concluded that C1q or IgM nephropathy variants do not seem to signify a worse prognosis in children with MCNS in comparison with IF-negative MCNS.
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Metadata
Title
Do C1q or IgM nephropathies predict disease severity in children with minimal change nephrotic syndrome?
Authors
Mateja Vintar Spreitzer
Alenka Vizjak
Dušan Ferluga
Rajko B. Kenda
Tanja Kersnik Levart
Publication date
01-01-2014
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Nephrology / Issue 1/2014
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-013-2551-3

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