Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classification
Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, pa...
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creator | Sethi, Sanjeev Beck, Laurence H. Glassock, Richard J. Haas, Mark De Vriese, An S. Caza, Tiffany N. Hoxha, Elion Lambeau, Gérard Tomas, Nicola M. Madden, Benjamin Debiec, Hanna D’Agati, Vivette D. Alexander, Mariam P. Amer, Hatem Appel, Gerald B. Barbour, Sean J. Caravaca-Fontan, Fernando Cattran, Daniel C. Casal Moura, Marta D’Avila, Domingos O. Eick, Renato G. Garovic, Vesna D. Greene, Eddie L. Herrera Hernandez, Loren P. Jennette, J. Charles Lieske, John C. Markowitz, Glen S. Nath, Karl A. Nasr, Samih H. Nast, Cynthia C. Pani, Antonello Praga, Manuel Remuzzi, Giuseppe Rennke, Helmut G. Ruggenenti, Piero Roccatello, Dario Soler, Maria Jose Specks, Ulrich Stahl, Rolf A.K. Singh, Raman Deep Theis, Jason D. Velosa, Jorge A. Wetzels, Jack F.M. Winearls, Christopher G. Yandian, Federico Zand, Ladan Ronco, Pierre Fervenza, Fernando C. |
description | Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%–90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment. |
doi_str_mv | 10.1016/j.kint.2023.06.032 |
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Charles ; Lieske, John C. ; Markowitz, Glen S. ; Nath, Karl A. ; Nasr, Samih H. ; Nast, Cynthia C. ; Pani, Antonello ; Praga, Manuel ; Remuzzi, Giuseppe ; Rennke, Helmut G. ; Ruggenenti, Piero ; Roccatello, Dario ; Soler, Maria Jose ; Specks, Ulrich ; Stahl, Rolf A.K. ; Singh, Raman Deep ; Theis, Jason D. ; Velosa, Jorge A. ; Wetzels, Jack F.M. ; Winearls, Christopher G. ; Yandian, Federico ; Zand, Ladan ; Ronco, Pierre ; Fervenza, Fernando C.</creator><creatorcontrib>Sethi, Sanjeev ; Beck, Laurence H. ; Glassock, Richard J. ; Haas, Mark ; De Vriese, An S. ; Caza, Tiffany N. ; Hoxha, Elion ; Lambeau, Gérard ; Tomas, Nicola M. ; Madden, Benjamin ; Debiec, Hanna ; D’Agati, Vivette D. ; Alexander, Mariam P. ; Amer, Hatem ; Appel, Gerald B. ; Barbour, Sean J. ; Caravaca-Fontan, Fernando ; Cattran, Daniel C. ; Casal Moura, Marta ; D’Avila, Domingos O. ; Eick, Renato G. ; Garovic, Vesna D. ; Greene, Eddie L. ; Herrera Hernandez, Loren P. ; Jennette, J. Charles ; Lieske, John C. ; Markowitz, Glen S. ; Nath, Karl A. ; Nasr, Samih H. ; Nast, Cynthia C. ; Pani, Antonello ; Praga, Manuel ; Remuzzi, Giuseppe ; Rennke, Helmut G. ; Ruggenenti, Piero ; Roccatello, Dario ; Soler, Maria Jose ; Specks, Ulrich ; Stahl, Rolf A.K. ; Singh, Raman Deep ; Theis, Jason D. ; Velosa, Jorge A. ; Wetzels, Jack F.M. ; Winearls, Christopher G. ; Yandian, Federico ; Zand, Ladan ; Ronco, Pierre ; Fervenza, Fernando C.</creatorcontrib><description>Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%–90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment.</description><identifier>ISSN: 0085-2538</identifier><identifier>EISSN: 1523-1755</identifier><identifier>DOI: 10.1016/j.kint.2023.06.032</identifier><identifier>PMID: 37795587</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Autoantibodies ; classification ; Consensus ; Glomerular Basement Membrane - pathology ; Glomerulonephritis, Membranous - diagnosis ; Glomerulonephritis, Membranous - therapy ; Humans ; Life Sciences ; membranous nephropathy ; Nephrectomy ; Receptors, Phospholipase A2 ; target antigens</subject><ispartof>Kidney international, 2023-12, Vol.104 (6), p.1092-1102</ispartof><rights>2023 International Society of Nephrology and Mayo Foundation for Medical Education and Research</rights><rights>Copyright © 2023 International Society of Nephrology and Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-6e215a0ad0263a94c3e382bfb07df2998f079b9574284b31b09d9bb403d997373</citedby><cites>FETCH-LOGICAL-c434t-6e215a0ad0263a94c3e382bfb07df2998f079b9574284b31b09d9bb403d997373</cites><orcidid>0000-0002-9239-518X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37795587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04263636$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sethi, Sanjeev</creatorcontrib><creatorcontrib>Beck, Laurence H.</creatorcontrib><creatorcontrib>Glassock, Richard J.</creatorcontrib><creatorcontrib>Haas, Mark</creatorcontrib><creatorcontrib>De Vriese, An S.</creatorcontrib><creatorcontrib>Caza, Tiffany N.</creatorcontrib><creatorcontrib>Hoxha, Elion</creatorcontrib><creatorcontrib>Lambeau, Gérard</creatorcontrib><creatorcontrib>Tomas, Nicola M.</creatorcontrib><creatorcontrib>Madden, Benjamin</creatorcontrib><creatorcontrib>Debiec, Hanna</creatorcontrib><creatorcontrib>D’Agati, Vivette D.</creatorcontrib><creatorcontrib>Alexander, Mariam P.</creatorcontrib><creatorcontrib>Amer, Hatem</creatorcontrib><creatorcontrib>Appel, Gerald B.</creatorcontrib><creatorcontrib>Barbour, Sean J.</creatorcontrib><creatorcontrib>Caravaca-Fontan, Fernando</creatorcontrib><creatorcontrib>Cattran, Daniel C.</creatorcontrib><creatorcontrib>Casal Moura, Marta</creatorcontrib><creatorcontrib>D’Avila, Domingos O.</creatorcontrib><creatorcontrib>Eick, Renato G.</creatorcontrib><creatorcontrib>Garovic, Vesna D.</creatorcontrib><creatorcontrib>Greene, Eddie L.</creatorcontrib><creatorcontrib>Herrera Hernandez, Loren P.</creatorcontrib><creatorcontrib>Jennette, J. Charles</creatorcontrib><creatorcontrib>Lieske, John C.</creatorcontrib><creatorcontrib>Markowitz, Glen S.</creatorcontrib><creatorcontrib>Nath, Karl A.</creatorcontrib><creatorcontrib>Nasr, Samih H.</creatorcontrib><creatorcontrib>Nast, Cynthia C.</creatorcontrib><creatorcontrib>Pani, Antonello</creatorcontrib><creatorcontrib>Praga, Manuel</creatorcontrib><creatorcontrib>Remuzzi, Giuseppe</creatorcontrib><creatorcontrib>Rennke, Helmut G.</creatorcontrib><creatorcontrib>Ruggenenti, Piero</creatorcontrib><creatorcontrib>Roccatello, Dario</creatorcontrib><creatorcontrib>Soler, Maria Jose</creatorcontrib><creatorcontrib>Specks, Ulrich</creatorcontrib><creatorcontrib>Stahl, Rolf A.K.</creatorcontrib><creatorcontrib>Singh, Raman Deep</creatorcontrib><creatorcontrib>Theis, Jason D.</creatorcontrib><creatorcontrib>Velosa, Jorge A.</creatorcontrib><creatorcontrib>Wetzels, Jack F.M.</creatorcontrib><creatorcontrib>Winearls, Christopher G.</creatorcontrib><creatorcontrib>Yandian, Federico</creatorcontrib><creatorcontrib>Zand, Ladan</creatorcontrib><creatorcontrib>Ronco, Pierre</creatorcontrib><creatorcontrib>Fervenza, Fernando C.</creatorcontrib><title>Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classification</title><title>Kidney international</title><addtitle>Kidney Int</addtitle><description>Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%–90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment.</description><subject>Autoantibodies</subject><subject>classification</subject><subject>Consensus</subject><subject>Glomerular Basement Membrane - pathology</subject><subject>Glomerulonephritis, Membranous - diagnosis</subject><subject>Glomerulonephritis, Membranous - therapy</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>membranous nephropathy</subject><subject>Nephrectomy</subject><subject>Receptors, Phospholipase A2</subject><subject>target antigens</subject><issn>0085-2538</issn><issn>1523-1755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu3CAQhlHVqtmkfYEeKo7Nwe4Axpiql2jVNJU2yiU99YAAYy1bG1zwrrRvH7ab5liNxAyjb37B_Ah9IFATIO3nXf3bh6WmQFkNbQ2MvkIrwimriOD8NVoBdLyinHUX6DLnHZS7ZPAWXTAhJOedWKFf9_oY8Xr0wVtsY8gu5H3Gyc0xLTgGPLnJJB1iaQY3b1Oc9bI9fsFzqWLWIx5iwhqHeHAjtqPO2Q_e6sXH8A69GfSY3fvnfIV-3n57XN9Vm4fvP9Y3m8o2rFmq1lHCNegeaMu0bCxzrKNmMCD6gUrZDSCkkVw0tGsMIwZkL41pgPVSCibYFbo-6271qObkJ52OKmqv7m426tSDpiiXOJDCfjqz5f1_9i4vavLZunHUwZU_KtoJRjmUo6D0jNoUc05ueNEmoE4GqJ06GaBOBihoFfwd-visvzeT619G_m28AF_PgCsbOXiXVLbeBet6n5xdVB_9__SfAHQllq4</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Sethi, Sanjeev</creator><creator>Beck, Laurence H.</creator><creator>Glassock, Richard J.</creator><creator>Haas, Mark</creator><creator>De Vriese, An S.</creator><creator>Caza, Tiffany N.</creator><creator>Hoxha, Elion</creator><creator>Lambeau, Gérard</creator><creator>Tomas, Nicola M.</creator><creator>Madden, Benjamin</creator><creator>Debiec, Hanna</creator><creator>D’Agati, Vivette D.</creator><creator>Alexander, Mariam P.</creator><creator>Amer, Hatem</creator><creator>Appel, Gerald B.</creator><creator>Barbour, Sean J.</creator><creator>Caravaca-Fontan, Fernando</creator><creator>Cattran, Daniel C.</creator><creator>Casal Moura, Marta</creator><creator>D’Avila, Domingos O.</creator><creator>Eick, Renato G.</creator><creator>Garovic, Vesna D.</creator><creator>Greene, Eddie L.</creator><creator>Herrera Hernandez, Loren P.</creator><creator>Jennette, J. 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Charles ; Lieske, John C. ; Markowitz, Glen S. ; Nath, Karl A. ; Nasr, Samih H. ; Nast, Cynthia C. ; Pani, Antonello ; Praga, Manuel ; Remuzzi, Giuseppe ; Rennke, Helmut G. ; Ruggenenti, Piero ; Roccatello, Dario ; Soler, Maria Jose ; Specks, Ulrich ; Stahl, Rolf A.K. ; Singh, Raman Deep ; Theis, Jason D. ; Velosa, Jorge A. ; Wetzels, Jack F.M. ; Winearls, Christopher G. ; Yandian, Federico ; Zand, Ladan ; Ronco, Pierre ; Fervenza, Fernando C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-6e215a0ad0263a94c3e382bfb07df2998f079b9574284b31b09d9bb403d997373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Autoantibodies</topic><topic>classification</topic><topic>Consensus</topic><topic>Glomerular Basement Membrane - pathology</topic><topic>Glomerulonephritis, Membranous - diagnosis</topic><topic>Glomerulonephritis, Membranous - therapy</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>membranous nephropathy</topic><topic>Nephrectomy</topic><topic>Receptors, Phospholipase A2</topic><topic>target antigens</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sethi, Sanjeev</creatorcontrib><creatorcontrib>Beck, Laurence H.</creatorcontrib><creatorcontrib>Glassock, Richard J.</creatorcontrib><creatorcontrib>Haas, Mark</creatorcontrib><creatorcontrib>De Vriese, An S.</creatorcontrib><creatorcontrib>Caza, Tiffany N.</creatorcontrib><creatorcontrib>Hoxha, Elion</creatorcontrib><creatorcontrib>Lambeau, Gérard</creatorcontrib><creatorcontrib>Tomas, Nicola M.</creatorcontrib><creatorcontrib>Madden, Benjamin</creatorcontrib><creatorcontrib>Debiec, Hanna</creatorcontrib><creatorcontrib>D’Agati, Vivette D.</creatorcontrib><creatorcontrib>Alexander, Mariam P.</creatorcontrib><creatorcontrib>Amer, Hatem</creatorcontrib><creatorcontrib>Appel, Gerald B.</creatorcontrib><creatorcontrib>Barbour, Sean J.</creatorcontrib><creatorcontrib>Caravaca-Fontan, Fernando</creatorcontrib><creatorcontrib>Cattran, Daniel C.</creatorcontrib><creatorcontrib>Casal Moura, Marta</creatorcontrib><creatorcontrib>D’Avila, Domingos O.</creatorcontrib><creatorcontrib>Eick, Renato G.</creatorcontrib><creatorcontrib>Garovic, Vesna D.</creatorcontrib><creatorcontrib>Greene, Eddie L.</creatorcontrib><creatorcontrib>Herrera Hernandez, Loren P.</creatorcontrib><creatorcontrib>Jennette, J. 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Charles</au><au>Lieske, John C.</au><au>Markowitz, Glen S.</au><au>Nath, Karl A.</au><au>Nasr, Samih H.</au><au>Nast, Cynthia C.</au><au>Pani, Antonello</au><au>Praga, Manuel</au><au>Remuzzi, Giuseppe</au><au>Rennke, Helmut G.</au><au>Ruggenenti, Piero</au><au>Roccatello, Dario</au><au>Soler, Maria Jose</au><au>Specks, Ulrich</au><au>Stahl, Rolf A.K.</au><au>Singh, Raman Deep</au><au>Theis, Jason D.</au><au>Velosa, Jorge A.</au><au>Wetzels, Jack F.M.</au><au>Winearls, Christopher G.</au><au>Yandian, Federico</au><au>Zand, Ladan</au><au>Ronco, Pierre</au><au>Fervenza, Fernando C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classification</atitle><jtitle>Kidney international</jtitle><addtitle>Kidney Int</addtitle><date>2023-12-01</date><risdate>2023</risdate><volume>104</volume><issue>6</issue><spage>1092</spage><epage>1102</epage><pages>1092-1102</pages><issn>0085-2538</issn><eissn>1523-1755</eissn><abstract>Membranous nephropathy (MN) is a pattern of injury caused by autoantibodies binding to specific target antigens, with accumulation of immune complexes along the subepithelial region of glomerular basement membranes. The past 20 years have brought revolutionary advances in the understanding of MN, particularly via the discovery of novel target antigens and their respective autoantibodies. These discoveries have challenged the traditional classification of MN into primary and secondary forms. At least 14 target antigens have been identified, accounting for 80%–90% of cases of MN. Many of the forms of MN associated with these novel MN target antigens have distinctive clinical and pathologic phenotypes. The Mayo Clinic consensus report on MN proposes a 2-step classification of MN. The first step, when possible, is identification of the target antigen, based on a multistep algorithm and using a combination of serology, staining of the kidney biopsy tissue by immunofluorescence or immunohistochemistry, and/or mass spectrometry methodology. The second step is the search for a potential underlying disease or associated condition, which is particularly relevant when knowledge of the target antigen is available to direct it. The meeting acknowledges that the resources and equipment required to perform the proposed testing may not be generally available. However, the meeting consensus was that the time has come to adopt an antigen-based classification of MN because this approach will allow for accurate and specific MN diagnosis, with significant implications for patient management and targeted treatment.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37795587</pmid><doi>10.1016/j.kint.2023.06.032</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9239-518X</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 0085-2538 |
ispartof | Kidney international, 2023-12, Vol.104 (6), p.1092-1102 |
issn | 0085-2538 1523-1755 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_04263636v1 |
source | MEDLINE; Alma/SFX Local Collection |
subjects | Autoantibodies classification Consensus Glomerular Basement Membrane - pathology Glomerulonephritis, Membranous - diagnosis Glomerulonephritis, Membranous - therapy Humans Life Sciences membranous nephropathy Nephrectomy Receptors, Phospholipase A2 target antigens |
title | Mayo Clinic consensus report on membranous nephropathy: proposal for a novel classification |
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