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Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings

BACKGROUND: In Henoch–Schönlein nephritis (HSN), a risk factor for unfavorable outcome is prolonged proteinuria, but the value of renal biopsies in prognosis assessment is debatable. METHODS: We evaluated serial renal biopsies from 26 HSN patients. Follow-up biopsy occurred at median 2.1 years after...

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Autores principales: Koskela, Mikael, Ylinen, Elisa, Autio-Harmainen, Helena, Tokola, Heikki, Heikkilä, Päivi, Lohi, Jouko, Jalanko, Hannu, Nuutinen, Matti, Jahnukainen, Timo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056733/
https://www.ncbi.nlm.nih.gov/pubmed/31797094
http://dx.doi.org/10.1007/s00467-019-04415-3
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author Koskela, Mikael
Ylinen, Elisa
Autio-Harmainen, Helena
Tokola, Heikki
Heikkilä, Päivi
Lohi, Jouko
Jalanko, Hannu
Nuutinen, Matti
Jahnukainen, Timo
author_facet Koskela, Mikael
Ylinen, Elisa
Autio-Harmainen, Helena
Tokola, Heikki
Heikkilä, Päivi
Lohi, Jouko
Jalanko, Hannu
Nuutinen, Matti
Jahnukainen, Timo
author_sort Koskela, Mikael
collection PubMed
description BACKGROUND: In Henoch–Schönlein nephritis (HSN), a risk factor for unfavorable outcome is prolonged proteinuria, but the value of renal biopsies in prognosis assessment is debatable. METHODS: We evaluated serial renal biopsies from 26 HSN patients. Follow-up biopsy occurred at median 2.1 years after diagnostic biopsy. Patients formed two groups at the follow-up biopsy: patients without proteinuria (group I; n = 11) and with proteinuria (group II; n = 15). Biopsies underwent evaluation according to three classifications: International Study of Kidney Disease in Children (ISKDC), Oxford (MEST-C), and semiquantitative classification (SQC) including an activity and chronicity score. Analysis also included expression of pro-fibrotic (alpha-smooth muscle actin and vimentin) and inflammatory (P-selectin glycoprotein ligand-1) molecules in the diagnostic biopsy specimens. Definition of unfavorable outcome was active renal disease or reduced renal function at last follow-up. RESULTS: Between the biopsies, SQC chronicity score increased in 22 (85%) patients, whereas activity score and ISKDC grade decreased in 21 (81%) and 17 (65%), respectively. Of the MEST-C parameters, endocapillary proliferation (from 83 to 13%; p < 0.001) and crescents (from 63 to 25%; p = 0.022) showed significant reduction, and segmental glomerulosclerosis (from 38 to 79%; p = 0.006) significant increment. These changes occurred similarly in groups I and II. Expression of the pro-fibrotic and inflammatory molecules showed no clinically significant differences between groups I and II. None in group I and five (33%) patients in group II had unfavorable outcome (p = 0.053). CONCLUSIONS: Our results suggest that follow-up biopsies provide limited additional information to clinical symptoms in HSN outcome prediction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00467-019-04415-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-70567332020-03-16 Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings Koskela, Mikael Ylinen, Elisa Autio-Harmainen, Helena Tokola, Heikki Heikkilä, Päivi Lohi, Jouko Jalanko, Hannu Nuutinen, Matti Jahnukainen, Timo Pediatr Nephrol Original Article BACKGROUND: In Henoch–Schönlein nephritis (HSN), a risk factor for unfavorable outcome is prolonged proteinuria, but the value of renal biopsies in prognosis assessment is debatable. METHODS: We evaluated serial renal biopsies from 26 HSN patients. Follow-up biopsy occurred at median 2.1 years after diagnostic biopsy. Patients formed two groups at the follow-up biopsy: patients without proteinuria (group I; n = 11) and with proteinuria (group II; n = 15). Biopsies underwent evaluation according to three classifications: International Study of Kidney Disease in Children (ISKDC), Oxford (MEST-C), and semiquantitative classification (SQC) including an activity and chronicity score. Analysis also included expression of pro-fibrotic (alpha-smooth muscle actin and vimentin) and inflammatory (P-selectin glycoprotein ligand-1) molecules in the diagnostic biopsy specimens. Definition of unfavorable outcome was active renal disease or reduced renal function at last follow-up. RESULTS: Between the biopsies, SQC chronicity score increased in 22 (85%) patients, whereas activity score and ISKDC grade decreased in 21 (81%) and 17 (65%), respectively. Of the MEST-C parameters, endocapillary proliferation (from 83 to 13%; p < 0.001) and crescents (from 63 to 25%; p = 0.022) showed significant reduction, and segmental glomerulosclerosis (from 38 to 79%; p = 0.006) significant increment. These changes occurred similarly in groups I and II. Expression of the pro-fibrotic and inflammatory molecules showed no clinically significant differences between groups I and II. None in group I and five (33%) patients in group II had unfavorable outcome (p = 0.053). CONCLUSIONS: Our results suggest that follow-up biopsies provide limited additional information to clinical symptoms in HSN outcome prediction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00467-019-04415-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-12-03 2020 /pmc/articles/PMC7056733/ /pubmed/31797094 http://dx.doi.org/10.1007/s00467-019-04415-3 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Koskela, Mikael
Ylinen, Elisa
Autio-Harmainen, Helena
Tokola, Heikki
Heikkilä, Päivi
Lohi, Jouko
Jalanko, Hannu
Nuutinen, Matti
Jahnukainen, Timo
Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title_full Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title_fullStr Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title_full_unstemmed Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title_short Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
title_sort prediction of renal outcome in henoch–schönlein nephritis based on biopsy findings
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056733/
https://www.ncbi.nlm.nih.gov/pubmed/31797094
http://dx.doi.org/10.1007/s00467-019-04415-3
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