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Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as prognostic markers in idiopathic membranous nephropathy

Background Urinary excretion of alpha-1-microglobulin and beta-2-microglobulin reflects tubular damage and predicts outcome in patients with idiopathic membranous nephropathy with reasonable accuracy. Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin are novel biomarker...

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Published in:Annals of clinical biochemistry 2016-01, Vol.53 (1), p.51-57
Main Authors: Maas, Rutger JH, van den Brand, Jan AJG, Waanders, Femke, Meijer, Esther, Goor van, Harry, Peters, Hilde P, Hofstra, Julia M, Wetzels, Jack FM
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container_title Annals of clinical biochemistry
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van den Brand, Jan AJG
Waanders, Femke
Meijer, Esther
Goor van, Harry
Peters, Hilde P
Hofstra, Julia M
Wetzels, Jack FM
description Background Urinary excretion of alpha-1-microglobulin and beta-2-microglobulin reflects tubular damage and predicts outcome in patients with idiopathic membranous nephropathy with reasonable accuracy. Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin are novel biomarkers of tubular damage. We investigated if these markers could improve prediction of outcome in idiopathic membranous nephropathy. Methods We measured kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin in urine samples from patients with idiopathic membranous nephropathy, who had nephrotic proteinuria and normal renal function. Excretion of alpha-1-microglobulin and beta-2-microglobulin had been measured previously. Progression was defined as a serum creatinine rise >30%, a rise in serum creatinine to an absolute value of ≥135 µmol/L, or a clinical decision to start immunosuppressive therapy. Remission was defined as proteinuria 50% reduction from baseline. Results Sixty-nine patients were included. Median follow-up was 35 months (interquartile range 18–63 months). Progression occurred in 30 patients (44%), and spontaneous remission in 36 (52%). Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates were significantly correlated with each other, and with alpha-1-microglobulin and beta-2-microglobulin. The areas under the receiver operating characteristic curves for progression were 0.75 (0.62–0.87) for kidney injury molecule-1 and 0.74 (0.62–0.87) for neutrophil gelatinase-associated lipocalin. In multivariate analysis with either alpha-1-microglobulin and beta-2-microglobulin, kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin did not independently predict outcome. Conclusion Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates correlated with excretion rates of other tubular damage markers and predicted outcome in patients with idiopathic membranous nephropathy. They did not add prognostic value compared to measurement of either alpha-1-microglobulin or beta-2-microglobulin.
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Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin are novel biomarkers of tubular damage. We investigated if these markers could improve prediction of outcome in idiopathic membranous nephropathy. Methods We measured kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin in urine samples from patients with idiopathic membranous nephropathy, who had nephrotic proteinuria and normal renal function. Excretion of alpha-1-microglobulin and beta-2-microglobulin had been measured previously. Progression was defined as a serum creatinine rise &gt;30%, a rise in serum creatinine to an absolute value of ≥135 µmol/L, or a clinical decision to start immunosuppressive therapy. Remission was defined as proteinuria &lt;3.5 g/day and &gt;50% reduction from baseline. Results Sixty-nine patients were included. Median follow-up was 35 months (interquartile range 18–63 months). Progression occurred in 30 patients (44%), and spontaneous remission in 36 (52%). Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates were significantly correlated with each other, and with alpha-1-microglobulin and beta-2-microglobulin. The areas under the receiver operating characteristic curves for progression were 0.75 (0.62–0.87) for kidney injury molecule-1 and 0.74 (0.62–0.87) for neutrophil gelatinase-associated lipocalin. In multivariate analysis with either alpha-1-microglobulin and beta-2-microglobulin, kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin did not independently predict outcome. Conclusion Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates correlated with excretion rates of other tubular damage markers and predicted outcome in patients with idiopathic membranous nephropathy. They did not add prognostic value compared to measurement of either alpha-1-microglobulin or beta-2-microglobulin.</description><identifier>ISSN: 0004-5632</identifier><identifier>EISSN: 1758-1001</identifier><identifier>DOI: 10.1177/0004563215579694</identifier><identifier>PMID: 25762211</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Acute-Phase Proteins - urine ; Adult ; Biomarkers - urine ; Female ; Glomerulonephritis, Membranous - diagnosis ; Glomerulonephritis, Membranous - urine ; Hepatitis A Virus Cellular Receptor 1 ; Humans ; Lipocalin-2 ; Lipocalins - urine ; Male ; Membrane Glycoproteins - urine ; Middle Aged ; Prognosis ; Proto-Oncogene Proteins - urine ; Receptors, Virus</subject><ispartof>Annals of clinical biochemistry, 2016-01, Vol.53 (1), p.51-57</ispartof><rights>The Author(s) 2015</rights><rights>The Author(s) 2015.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-1630a48e1b8c4a215b2c57760fb8bf4429b1928fc0920adb7cbceaadf6490223</citedby><cites>FETCH-LOGICAL-c412t-1630a48e1b8c4a215b2c57760fb8bf4429b1928fc0920adb7cbceaadf6490223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25762211$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maas, Rutger JH</creatorcontrib><creatorcontrib>van den Brand, Jan AJG</creatorcontrib><creatorcontrib>Waanders, Femke</creatorcontrib><creatorcontrib>Meijer, Esther</creatorcontrib><creatorcontrib>Goor van, Harry</creatorcontrib><creatorcontrib>Peters, Hilde P</creatorcontrib><creatorcontrib>Hofstra, Julia M</creatorcontrib><creatorcontrib>Wetzels, Jack FM</creatorcontrib><title>Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as prognostic markers in idiopathic membranous nephropathy</title><title>Annals of clinical biochemistry</title><addtitle>Ann Clin Biochem</addtitle><description>Background Urinary excretion of alpha-1-microglobulin and beta-2-microglobulin reflects tubular damage and predicts outcome in patients with idiopathic membranous nephropathy with reasonable accuracy. Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin are novel biomarkers of tubular damage. We investigated if these markers could improve prediction of outcome in idiopathic membranous nephropathy. Methods We measured kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin in urine samples from patients with idiopathic membranous nephropathy, who had nephrotic proteinuria and normal renal function. Excretion of alpha-1-microglobulin and beta-2-microglobulin had been measured previously. Progression was defined as a serum creatinine rise &gt;30%, a rise in serum creatinine to an absolute value of ≥135 µmol/L, or a clinical decision to start immunosuppressive therapy. Remission was defined as proteinuria &lt;3.5 g/day and &gt;50% reduction from baseline. Results Sixty-nine patients were included. Median follow-up was 35 months (interquartile range 18–63 months). Progression occurred in 30 patients (44%), and spontaneous remission in 36 (52%). Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates were significantly correlated with each other, and with alpha-1-microglobulin and beta-2-microglobulin. The areas under the receiver operating characteristic curves for progression were 0.75 (0.62–0.87) for kidney injury molecule-1 and 0.74 (0.62–0.87) for neutrophil gelatinase-associated lipocalin. In multivariate analysis with either alpha-1-microglobulin and beta-2-microglobulin, kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin did not independently predict outcome. Conclusion Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates correlated with excretion rates of other tubular damage markers and predicted outcome in patients with idiopathic membranous nephropathy. They did not add prognostic value compared to measurement of either alpha-1-microglobulin or beta-2-microglobulin.</description><subject>Acute-Phase Proteins - urine</subject><subject>Adult</subject><subject>Biomarkers - urine</subject><subject>Female</subject><subject>Glomerulonephritis, Membranous - diagnosis</subject><subject>Glomerulonephritis, Membranous - urine</subject><subject>Hepatitis A Virus Cellular Receptor 1</subject><subject>Humans</subject><subject>Lipocalin-2</subject><subject>Lipocalins - urine</subject><subject>Male</subject><subject>Membrane Glycoproteins - urine</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Proto-Oncogene Proteins - urine</subject><subject>Receptors, Virus</subject><issn>0004-5632</issn><issn>1758-1001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU2P1DAMhiMEYmcX7pxQjlwKcZo27RGt-NKuxGXvlZO6MxnSpCTtYa78cjLMwgEJiZNl-_Uj2y9jr0C8BdD6nRBCNW0toWl03_bqCduBbroKhICnbHduV-f-FbvO-VhSqYV4zq5ko1spAXbsx50bA524C8ctnfgcPdnNUwUcw8gDbWuKy8F5viePqwuYqcKco3W40si9W6JF7wLHzJcU9yHm1Vk-Y_pGKRcsd6OLC66Hc5VmkzDELRfycki_6qcX7NmEPtPLx3jDHj5-eLj9XN1__fTl9v19ZRXItYK2Fqg6AtNZheVkI22jdSsm05lJKdkb6GU3WdFLgaPR1lhCHKdW9ULK-oa9uWDLmt83yuswu2zJewxUNhqgvKRulVTNf0gbgL4VfV2k4iK1KeacaBqW5Mr1pwHEcPZo-NujMvL6kb6ZmcY_A79NKYLqIsi4p-EYtxTKX_4N_AmiZZuQ</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Maas, Rutger JH</creator><creator>van den Brand, Jan AJG</creator><creator>Waanders, Femke</creator><creator>Meijer, Esther</creator><creator>Goor van, Harry</creator><creator>Peters, Hilde P</creator><creator>Hofstra, Julia M</creator><creator>Wetzels, Jack FM</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201601</creationdate><title>Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as prognostic markers in idiopathic membranous nephropathy</title><author>Maas, Rutger JH ; van den Brand, Jan AJG ; Waanders, Femke ; Meijer, Esther ; Goor van, Harry ; Peters, Hilde P ; Hofstra, Julia M ; Wetzels, Jack FM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-1630a48e1b8c4a215b2c57760fb8bf4429b1928fc0920adb7cbceaadf6490223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute-Phase Proteins - urine</topic><topic>Adult</topic><topic>Biomarkers - urine</topic><topic>Female</topic><topic>Glomerulonephritis, Membranous - diagnosis</topic><topic>Glomerulonephritis, Membranous - urine</topic><topic>Hepatitis A Virus Cellular Receptor 1</topic><topic>Humans</topic><topic>Lipocalin-2</topic><topic>Lipocalins - urine</topic><topic>Male</topic><topic>Membrane Glycoproteins - urine</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Proto-Oncogene Proteins - urine</topic><topic>Receptors, Virus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maas, Rutger JH</creatorcontrib><creatorcontrib>van den Brand, Jan AJG</creatorcontrib><creatorcontrib>Waanders, Femke</creatorcontrib><creatorcontrib>Meijer, Esther</creatorcontrib><creatorcontrib>Goor van, Harry</creatorcontrib><creatorcontrib>Peters, Hilde P</creatorcontrib><creatorcontrib>Hofstra, Julia M</creatorcontrib><creatorcontrib>Wetzels, Jack FM</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Annals of clinical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maas, Rutger JH</au><au>van den Brand, Jan AJG</au><au>Waanders, Femke</au><au>Meijer, Esther</au><au>Goor van, Harry</au><au>Peters, Hilde P</au><au>Hofstra, Julia M</au><au>Wetzels, Jack FM</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as prognostic markers in idiopathic membranous nephropathy</atitle><jtitle>Annals of clinical biochemistry</jtitle><addtitle>Ann Clin Biochem</addtitle><date>2016-01</date><risdate>2016</risdate><volume>53</volume><issue>1</issue><spage>51</spage><epage>57</epage><pages>51-57</pages><issn>0004-5632</issn><eissn>1758-1001</eissn><abstract>Background Urinary excretion of alpha-1-microglobulin and beta-2-microglobulin reflects tubular damage and predicts outcome in patients with idiopathic membranous nephropathy with reasonable accuracy. Urinary kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin are novel biomarkers of tubular damage. We investigated if these markers could improve prediction of outcome in idiopathic membranous nephropathy. Methods We measured kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin in urine samples from patients with idiopathic membranous nephropathy, who had nephrotic proteinuria and normal renal function. Excretion of alpha-1-microglobulin and beta-2-microglobulin had been measured previously. Progression was defined as a serum creatinine rise &gt;30%, a rise in serum creatinine to an absolute value of ≥135 µmol/L, or a clinical decision to start immunosuppressive therapy. Remission was defined as proteinuria &lt;3.5 g/day and &gt;50% reduction from baseline. Results Sixty-nine patients were included. Median follow-up was 35 months (interquartile range 18–63 months). Progression occurred in 30 patients (44%), and spontaneous remission in 36 (52%). Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates were significantly correlated with each other, and with alpha-1-microglobulin and beta-2-microglobulin. The areas under the receiver operating characteristic curves for progression were 0.75 (0.62–0.87) for kidney injury molecule-1 and 0.74 (0.62–0.87) for neutrophil gelatinase-associated lipocalin. In multivariate analysis with either alpha-1-microglobulin and beta-2-microglobulin, kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin did not independently predict outcome. Conclusion Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin excretion rates correlated with excretion rates of other tubular damage markers and predicted outcome in patients with idiopathic membranous nephropathy. They did not add prognostic value compared to measurement of either alpha-1-microglobulin or beta-2-microglobulin.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25762211</pmid><doi>10.1177/0004563215579694</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute-Phase Proteins - urine
Adult
Biomarkers - urine
Female
Glomerulonephritis, Membranous - diagnosis
Glomerulonephritis, Membranous - urine
Hepatitis A Virus Cellular Receptor 1
Humans
Lipocalin-2
Lipocalins - urine
Male
Membrane Glycoproteins - urine
Middle Aged
Prognosis
Proto-Oncogene Proteins - urine
Receptors, Virus
title Kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin as prognostic markers in idiopathic membranous nephropathy
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