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Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort

BACKGROUND: C3 glomerulopathy (C3G) is a rare kidney disorder characterized by predominant glomerular depositions of complement C3. C3G can be subdivided into dense deposit disease (DDD) and C3 glomerulonephritis (C3GN). This study describes the long-term follow-up with extensive complement analysis...

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Autores principales: Michels, Marloes A. H. M., Wijnsma, Kioa L., Kurvers, Roel A. J., Westra, Dineke, Schreuder, Michiel F., van Wijk, Joanna A. E., Bouts, Antonia H. M., Gracchi, Valentina, Engels, Flore A. P. T., Keijzer-Veen, Mandy G., Dorresteijn, Eiske M., Volokhina, Elena B., van den Heuvel, Lambertus P. W. J., van de Kar, Nicole C. A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921070/
https://www.ncbi.nlm.nih.gov/pubmed/34476601
http://dx.doi.org/10.1007/s00467-021-05221-6
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author Michels, Marloes A. H. M.
Wijnsma, Kioa L.
Kurvers, Roel A. J.
Westra, Dineke
Schreuder, Michiel F.
van Wijk, Joanna A. E.
Bouts, Antonia H. M.
Gracchi, Valentina
Engels, Flore A. P. T.
Keijzer-Veen, Mandy G.
Dorresteijn, Eiske M.
Volokhina, Elena B.
van den Heuvel, Lambertus P. W. J.
van de Kar, Nicole C. A. J.
author_facet Michels, Marloes A. H. M.
Wijnsma, Kioa L.
Kurvers, Roel A. J.
Westra, Dineke
Schreuder, Michiel F.
van Wijk, Joanna A. E.
Bouts, Antonia H. M.
Gracchi, Valentina
Engels, Flore A. P. T.
Keijzer-Veen, Mandy G.
Dorresteijn, Eiske M.
Volokhina, Elena B.
van den Heuvel, Lambertus P. W. J.
van de Kar, Nicole C. A. J.
author_sort Michels, Marloes A. H. M.
collection PubMed
description BACKGROUND: C3 glomerulopathy (C3G) is a rare kidney disorder characterized by predominant glomerular depositions of complement C3. C3G can be subdivided into dense deposit disease (DDD) and C3 glomerulonephritis (C3GN). This study describes the long-term follow-up with extensive complement analysis of 29 Dutch children with C3G. METHODS: Twenty-nine C3G patients (19 DDD, 10 C3GN) diagnosed between 1992 and 2014 were included. Clinical and laboratory findings were collected at presentation and during follow-up. Specialized assays were used to detect rare variants in complement genes and measure complement-directed autoantibodies and biomarkers in blood. RESULTS: DDD patients presented with lower estimated glomerular filtration rate (eGFR). C3 nephritic factors (C3NeFs) were detected in 20 patients and remained detectable over time despite immunosuppressive treatment. At presentation, low serum C3 levels were detected in 84% of all patients. During follow-up, in about 50% of patients, all of them C3NeF-positive, C3 levels remained low. Linear mixed model analysis showed that C3GN patients had higher soluble C5b-9 (sC5b-9) and lower properdin levels compared to DDD patients. With a median follow-up of 52 months, an overall benign outcome was observed with only six patients with eGFR below 90 ml/min/1.73 m(2) at last follow-up. CONCLUSIONS: We extensively described clinical and laboratory findings including complement features of an exclusively pediatric C3G cohort. Outcome was relatively benign, persistent low C3 correlated with C3NeF presence, and C3GN was associated with higher sC5b-9 and lower properdin levels. Prospective studies are needed to further elucidate the pathogenic mechanisms underlying C3G and guide personalized medicine with complement therapeutics. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-021-05221-6.
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spelling pubmed-89210702022-03-17 Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort Michels, Marloes A. H. M. Wijnsma, Kioa L. Kurvers, Roel A. J. Westra, Dineke Schreuder, Michiel F. van Wijk, Joanna A. E. Bouts, Antonia H. M. Gracchi, Valentina Engels, Flore A. P. T. Keijzer-Veen, Mandy G. Dorresteijn, Eiske M. Volokhina, Elena B. van den Heuvel, Lambertus P. W. J. van de Kar, Nicole C. A. J. Pediatr Nephrol Original Article BACKGROUND: C3 glomerulopathy (C3G) is a rare kidney disorder characterized by predominant glomerular depositions of complement C3. C3G can be subdivided into dense deposit disease (DDD) and C3 glomerulonephritis (C3GN). This study describes the long-term follow-up with extensive complement analysis of 29 Dutch children with C3G. METHODS: Twenty-nine C3G patients (19 DDD, 10 C3GN) diagnosed between 1992 and 2014 were included. Clinical and laboratory findings were collected at presentation and during follow-up. Specialized assays were used to detect rare variants in complement genes and measure complement-directed autoantibodies and biomarkers in blood. RESULTS: DDD patients presented with lower estimated glomerular filtration rate (eGFR). C3 nephritic factors (C3NeFs) were detected in 20 patients and remained detectable over time despite immunosuppressive treatment. At presentation, low serum C3 levels were detected in 84% of all patients. During follow-up, in about 50% of patients, all of them C3NeF-positive, C3 levels remained low. Linear mixed model analysis showed that C3GN patients had higher soluble C5b-9 (sC5b-9) and lower properdin levels compared to DDD patients. With a median follow-up of 52 months, an overall benign outcome was observed with only six patients with eGFR below 90 ml/min/1.73 m(2) at last follow-up. CONCLUSIONS: We extensively described clinical and laboratory findings including complement features of an exclusively pediatric C3G cohort. Outcome was relatively benign, persistent low C3 correlated with C3NeF presence, and C3GN was associated with higher sC5b-9 and lower properdin levels. Prospective studies are needed to further elucidate the pathogenic mechanisms underlying C3G and guide personalized medicine with complement therapeutics. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-021-05221-6. Springer Berlin Heidelberg 2021-09-02 2022 /pmc/articles/PMC8921070/ /pubmed/34476601 http://dx.doi.org/10.1007/s00467-021-05221-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Michels, Marloes A. H. M.
Wijnsma, Kioa L.
Kurvers, Roel A. J.
Westra, Dineke
Schreuder, Michiel F.
van Wijk, Joanna A. E.
Bouts, Antonia H. M.
Gracchi, Valentina
Engels, Flore A. P. T.
Keijzer-Veen, Mandy G.
Dorresteijn, Eiske M.
Volokhina, Elena B.
van den Heuvel, Lambertus P. W. J.
van de Kar, Nicole C. A. J.
Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title_full Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title_fullStr Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title_full_unstemmed Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title_short Long-term follow-up including extensive complement analysis of a pediatric C3 glomerulopathy cohort
title_sort long-term follow-up including extensive complement analysis of a pediatric c3 glomerulopathy cohort
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921070/
https://www.ncbi.nlm.nih.gov/pubmed/34476601
http://dx.doi.org/10.1007/s00467-021-05221-6
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