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Membranous Nephropathy: From Research Bench to Personalized Care

Membranous nephropathy is a glomerulopathy that causes nephrotic syndrome and, in at least a third of cases, lasting end-stage kidney disease (ESKD). It is also a rare case of revolutionary changes in our understanding of the disease, that translates from scientific findings to real diagnosis and tr...

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Autores principales: Moszczuk, Barbara, Kiryluk, Krzysztof, Pączek, Leszek, Mucha, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998937/
https://www.ncbi.nlm.nih.gov/pubmed/33799372
http://dx.doi.org/10.3390/jcm10061205
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author Moszczuk, Barbara
Kiryluk, Krzysztof
Pączek, Leszek
Mucha, Krzysztof
author_facet Moszczuk, Barbara
Kiryluk, Krzysztof
Pączek, Leszek
Mucha, Krzysztof
author_sort Moszczuk, Barbara
collection PubMed
description Membranous nephropathy is a glomerulopathy that causes nephrotic syndrome and, in at least a third of cases, lasting end-stage kidney disease (ESKD). It is also a rare case of revolutionary changes in our understanding of the disease, that translates from scientific findings to real diagnosis and treatment recommendations in less than ten years. In this review we present: (1) a short history and traditional approach to patients with membranous nephropathy, (2) current recommendations and treatment options that have emerged in recent years, (3) findings of new studies, with a particular focus on serological/immunological methods, genomic and proteomic studies, still requiring validation. With further development in this field, membranous nephropathy may become one of the first nephrological conditions that apply a truly personalized approach with the omission of invasive measures such as kidney biopsy.
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spelling pubmed-79989372021-03-28 Membranous Nephropathy: From Research Bench to Personalized Care Moszczuk, Barbara Kiryluk, Krzysztof Pączek, Leszek Mucha, Krzysztof J Clin Med Review Membranous nephropathy is a glomerulopathy that causes nephrotic syndrome and, in at least a third of cases, lasting end-stage kidney disease (ESKD). It is also a rare case of revolutionary changes in our understanding of the disease, that translates from scientific findings to real diagnosis and treatment recommendations in less than ten years. In this review we present: (1) a short history and traditional approach to patients with membranous nephropathy, (2) current recommendations and treatment options that have emerged in recent years, (3) findings of new studies, with a particular focus on serological/immunological methods, genomic and proteomic studies, still requiring validation. With further development in this field, membranous nephropathy may become one of the first nephrological conditions that apply a truly personalized approach with the omission of invasive measures such as kidney biopsy. MDPI 2021-03-14 /pmc/articles/PMC7998937/ /pubmed/33799372 http://dx.doi.org/10.3390/jcm10061205 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Moszczuk, Barbara
Kiryluk, Krzysztof
Pączek, Leszek
Mucha, Krzysztof
Membranous Nephropathy: From Research Bench to Personalized Care
title Membranous Nephropathy: From Research Bench to Personalized Care
title_full Membranous Nephropathy: From Research Bench to Personalized Care
title_fullStr Membranous Nephropathy: From Research Bench to Personalized Care
title_full_unstemmed Membranous Nephropathy: From Research Bench to Personalized Care
title_short Membranous Nephropathy: From Research Bench to Personalized Care
title_sort membranous nephropathy: from research bench to personalized care
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998937/
https://www.ncbi.nlm.nih.gov/pubmed/33799372
http://dx.doi.org/10.3390/jcm10061205
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