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First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator

Background: We have previously shown that metzincin protease ADAMTS-4 accompanies renal fibrogenesis, as it appears in the blood of hemodialysis patients. Methods: Native kidney (NKB) and kidney transplant (TXCI) biopsy samples as well as plasma from patients with various stages of CKD were compared...

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Autores principales: Vojtusek, Ivana Kovacevic, Laganovic, Mario, Burek Kamenaric, Marija, Bulimbasic, Stela, Hrkac, Stela, Salai, Grgur, Ivkovic, Vanja, Coric, Marijana, Novak, Rudjer, Grgurevic, Lovorka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947148/
https://www.ncbi.nlm.nih.gov/pubmed/35328201
http://dx.doi.org/10.3390/diagnostics12030648
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author Vojtusek, Ivana Kovacevic
Laganovic, Mario
Burek Kamenaric, Marija
Bulimbasic, Stela
Hrkac, Stela
Salai, Grgur
Ivkovic, Vanja
Coric, Marijana
Novak, Rudjer
Grgurevic, Lovorka
author_facet Vojtusek, Ivana Kovacevic
Laganovic, Mario
Burek Kamenaric, Marija
Bulimbasic, Stela
Hrkac, Stela
Salai, Grgur
Ivkovic, Vanja
Coric, Marijana
Novak, Rudjer
Grgurevic, Lovorka
author_sort Vojtusek, Ivana Kovacevic
collection PubMed
description Background: We have previously shown that metzincin protease ADAMTS-4 accompanies renal fibrogenesis, as it appears in the blood of hemodialysis patients. Methods: Native kidney (NKB) and kidney transplant (TXCI) biopsy samples as well as plasma from patients with various stages of CKD were compared to controls. In paired analysis, 15 TXCI samples were compared with their zero-time biopsies (TX0). Tissues were evaluated and scored (interstitial fibrosis and tubular atrophy (IFTA) for NKB and Banff ci for TXCI). Immunohistochemical (IHC) staining for ADAMTS-4 and BMP-1 was performed. Plasma ADAMTS-4 was detected using ELISA. Results: ADAMTS-4 IHC expression was significantly higher in interstitial compartment (INT) of NKB and TXCI group in peritubular capillaries (PTC) and interstitial stroma (INT). Patients with higher stages of interstitial fibrosis (ci > 1 and IFTA > 1) expressed ADAMTS-4 in INT more frequently in both groups (p = 0.005; p = 0.013; respectively). In paired comparison, TXCI samples expressed ADAMTS-4 in INT and PTC more often than TX0. ADAMTS-4 plasma concentration varied significantly across CKD stages, being highest in CKD 2 and 3 compared to other groups (p = 0.0064). Hemodialysis patients had higher concentrations of ADAMTS-4 compared to peritoneal dialysis (p < 0.00001). Conclusion: ADAMTS-4 might have a significant role in CKD as a potential novel diagnostic indicator.
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spelling pubmed-89471482022-03-25 First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator Vojtusek, Ivana Kovacevic Laganovic, Mario Burek Kamenaric, Marija Bulimbasic, Stela Hrkac, Stela Salai, Grgur Ivkovic, Vanja Coric, Marijana Novak, Rudjer Grgurevic, Lovorka Diagnostics (Basel) Article Background: We have previously shown that metzincin protease ADAMTS-4 accompanies renal fibrogenesis, as it appears in the blood of hemodialysis patients. Methods: Native kidney (NKB) and kidney transplant (TXCI) biopsy samples as well as plasma from patients with various stages of CKD were compared to controls. In paired analysis, 15 TXCI samples were compared with their zero-time biopsies (TX0). Tissues were evaluated and scored (interstitial fibrosis and tubular atrophy (IFTA) for NKB and Banff ci for TXCI). Immunohistochemical (IHC) staining for ADAMTS-4 and BMP-1 was performed. Plasma ADAMTS-4 was detected using ELISA. Results: ADAMTS-4 IHC expression was significantly higher in interstitial compartment (INT) of NKB and TXCI group in peritubular capillaries (PTC) and interstitial stroma (INT). Patients with higher stages of interstitial fibrosis (ci > 1 and IFTA > 1) expressed ADAMTS-4 in INT more frequently in both groups (p = 0.005; p = 0.013; respectively). In paired comparison, TXCI samples expressed ADAMTS-4 in INT and PTC more often than TX0. ADAMTS-4 plasma concentration varied significantly across CKD stages, being highest in CKD 2 and 3 compared to other groups (p = 0.0064). Hemodialysis patients had higher concentrations of ADAMTS-4 compared to peritoneal dialysis (p < 0.00001). Conclusion: ADAMTS-4 might have a significant role in CKD as a potential novel diagnostic indicator. MDPI 2022-03-07 /pmc/articles/PMC8947148/ /pubmed/35328201 http://dx.doi.org/10.3390/diagnostics12030648 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vojtusek, Ivana Kovacevic
Laganovic, Mario
Burek Kamenaric, Marija
Bulimbasic, Stela
Hrkac, Stela
Salai, Grgur
Ivkovic, Vanja
Coric, Marijana
Novak, Rudjer
Grgurevic, Lovorka
First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title_full First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title_fullStr First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title_full_unstemmed First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title_short First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
title_sort first characterization of adamts-4 in kidney tissue and plasma of patients with chronic kidney disease—a potential novel diagnostic indicator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947148/
https://www.ncbi.nlm.nih.gov/pubmed/35328201
http://dx.doi.org/10.3390/diagnostics12030648
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