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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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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. |
format | Online Article Text |
id | pubmed-7056733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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