SAT0413 Urinary Lipocalin-2 as a Biomarker of Renal Disease Activity in Patients with Lupus Nephritis: A Prospective Study

BackgroundLupus nephritis (LN) is a common manifestation among patients with systemic lupus erythematosus (SLE), occurring in over 50%. One major determinant of poor prognosis among patients with SLE is renal involvement (1). Available renal biomarkers that measure the degree of SLE renal disease ac...

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Veröffentlicht in:Annals of the rheumatic diseases 2015-06, Vol.74 (Suppl 2), p.808-809
Hauptverfasser: Gamal, N. M., Mustafa, N.M., Abda, E. A.M., Afifi, O., Fathi, N.
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Mustafa, N.M.
Abda, E. A.M.
Afifi, O.
Fathi, N.
description BackgroundLupus nephritis (LN) is a common manifestation among patients with systemic lupus erythematosus (SLE), occurring in over 50%. One major determinant of poor prognosis among patients with SLE is renal involvement (1). Available renal biomarkers that measure the degree of SLE renal disease activity are too insensitive to allow for early identification of patients with active SLE nephritis, prohibiting early initiation of therapy to avoid permanent renal damage (2). Lipocalin-2 was regarded a novel biomarker in various types of acute kidney injury and chronic kidney diseases (3,4).ObjectivesThe aim of this study was to detect the levels of urinary lipocalin-2 excretion in SLE patients, to determine its association with SLE disease activity focusing on nephritis and to assess its value in predicting changes of SLE disease activity.MethodsThe study included 50 adult SLE patients met 1997 revised ACR classification criteria for SLE and 20 matched healthy controls. Patients were clinically and laboratory evaluated. Activity was assessed using SLEDAI score. SLE patients were classified into 2 groups (with LN and without LN) based on renal parameters of SLEDAI score. Urinary lipocalin-2 levels were measured using ELISA in SLE patients and controls. Twenty five of included patients were enrolled in a longitudinal study one year after the initial visit. SLEDAI score, laboratory investigation and urinary lipocalin-2 levels were assessed and compared with their initial values.ResultsUrinary lipocalin-2 levels were significantly higher in SLE patients (13.2±2.44 ng/ml) compared with normal controls (1.70±0.23 ng/ml) (p=0.004). Among SLE patients, urinary lipocalin-2 levels were significantly higher in patients with LN (22.95±4.41 ng/ml; n=22) than in those without LN (5.39±1.54 ng/ml; n=28) (p=0.000). Urinary lipocalin-2 of patients with LN correlated significantly with the renal SLEDAI score (r=0.790, p=0.000), but not with extrarenal disease activity. Within follow up group, urinary lipocalin-2 levels showed significant difference when compared between with and without LN groups (p =0.016). Change in total and renal SLEDAI scores were associated with change of urinary lipocalin-2 levels within follow up group but none of these changes reached statistical significance.ConclusionsUrinary lipocalin-2 is a potential biomarker for renal disease activity in adult SLE patients and its serial measurements may be valuable in predict worsening of SLE disease activity.R
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M. ; Mustafa, N.M. ; Abda, E. A.M. ; Afifi, O. ; Fathi, N.</creator><creatorcontrib>Gamal, N. M. ; Mustafa, N.M. ; Abda, E. A.M. ; Afifi, O. ; Fathi, N.</creatorcontrib><description>BackgroundLupus nephritis (LN) is a common manifestation among patients with systemic lupus erythematosus (SLE), occurring in over 50%. One major determinant of poor prognosis among patients with SLE is renal involvement (1). Available renal biomarkers that measure the degree of SLE renal disease activity are too insensitive to allow for early identification of patients with active SLE nephritis, prohibiting early initiation of therapy to avoid permanent renal damage (2). Lipocalin-2 was regarded a novel biomarker in various types of acute kidney injury and chronic kidney diseases (3,4).ObjectivesThe aim of this study was to detect the levels of urinary lipocalin-2 excretion in SLE patients, to determine its association with SLE disease activity focusing on nephritis and to assess its value in predicting changes of SLE disease activity.MethodsThe study included 50 adult SLE patients met 1997 revised ACR classification criteria for SLE and 20 matched healthy controls. Patients were clinically and laboratory evaluated. Activity was assessed using SLEDAI score. SLE patients were classified into 2 groups (with LN and without LN) based on renal parameters of SLEDAI score. Urinary lipocalin-2 levels were measured using ELISA in SLE patients and controls. Twenty five of included patients were enrolled in a longitudinal study one year after the initial visit. SLEDAI score, laboratory investigation and urinary lipocalin-2 levels were assessed and compared with their initial values.ResultsUrinary lipocalin-2 levels were significantly higher in SLE patients (13.2±2.44 ng/ml) compared with normal controls (1.70±0.23 ng/ml) (p=0.004). Among SLE patients, urinary lipocalin-2 levels were significantly higher in patients with LN (22.95±4.41 ng/ml; n=22) than in those without LN (5.39±1.54 ng/ml; n=28) (p=0.000). Urinary lipocalin-2 of patients with LN correlated significantly with the renal SLEDAI score (r=0.790, p=0.000), but not with extrarenal disease activity. Within follow up group, urinary lipocalin-2 levels showed significant difference when compared between with and without LN groups (p =0.016). Change in total and renal SLEDAI scores were associated with change of urinary lipocalin-2 levels within follow up group but none of these changes reached statistical significance.ConclusionsUrinary lipocalin-2 is a potential biomarker for renal disease activity in adult SLE patients and its serial measurements may be valuable in predict worsening of SLE disease activity.ReferencesBastian HM, Alarcon GS, Roseman JM, McGwin G Jr, Vila LM, Fessler BJ, Reveille JD. Systemic lupus erythematosus in a multi-ethnic US cohort (LUMINA) XLII: Factors predictive of new or worsening proteinuria. Rheumatology 2007; 46:683–9Ho A, Barr SG, Magder LS, Petri M. A decrease in complement is associated with increased renal and hematologic activity in patients with systemic lupus erythematosus. Arthritis Rheum 2001; 44:2350–2357Bolignano D, Donato V, Coppolino G, Campo S, Buemi A, Lacquaniti A, Beumi M. Neutrophil gelatinase-associated lipocalin (NGAL) as a marker of kidney damage, American Journal of Kidney Diseases 2008; vol. 52, no. 3, 595–605Rubinstein T, Pitashny M and Putterman C. The novel role of neutrophil gelatinase-B associated lipocalin (NGAL)/ Lipocalin-2 as a biomarker for lupus nephritis. Autoimmunity Reviews vol 7 2008; no. 3, 229–234Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2015-eular.1871</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><ispartof>Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.808-809</ispartof><rights>2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2015 (c) 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/74/Suppl_2/808.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/74/Suppl_2/808.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77342,77373</link.rule.ids></links><search><creatorcontrib>Gamal, N. M.</creatorcontrib><creatorcontrib>Mustafa, N.M.</creatorcontrib><creatorcontrib>Abda, E. A.M.</creatorcontrib><creatorcontrib>Afifi, O.</creatorcontrib><creatorcontrib>Fathi, N.</creatorcontrib><title>SAT0413 Urinary Lipocalin-2 as a Biomarker of Renal Disease Activity in Patients with Lupus Nephritis: A Prospective Study</title><title>Annals of the rheumatic diseases</title><description>BackgroundLupus nephritis (LN) is a common manifestation among patients with systemic lupus erythematosus (SLE), occurring in over 50%. One major determinant of poor prognosis among patients with SLE is renal involvement (1). Available renal biomarkers that measure the degree of SLE renal disease activity are too insensitive to allow for early identification of patients with active SLE nephritis, prohibiting early initiation of therapy to avoid permanent renal damage (2). Lipocalin-2 was regarded a novel biomarker in various types of acute kidney injury and chronic kidney diseases (3,4).ObjectivesThe aim of this study was to detect the levels of urinary lipocalin-2 excretion in SLE patients, to determine its association with SLE disease activity focusing on nephritis and to assess its value in predicting changes of SLE disease activity.MethodsThe study included 50 adult SLE patients met 1997 revised ACR classification criteria for SLE and 20 matched healthy controls. Patients were clinically and laboratory evaluated. Activity was assessed using SLEDAI score. SLE patients were classified into 2 groups (with LN and without LN) based on renal parameters of SLEDAI score. Urinary lipocalin-2 levels were measured using ELISA in SLE patients and controls. Twenty five of included patients were enrolled in a longitudinal study one year after the initial visit. SLEDAI score, laboratory investigation and urinary lipocalin-2 levels were assessed and compared with their initial values.ResultsUrinary lipocalin-2 levels were significantly higher in SLE patients (13.2±2.44 ng/ml) compared with normal controls (1.70±0.23 ng/ml) (p=0.004). Among SLE patients, urinary lipocalin-2 levels were significantly higher in patients with LN (22.95±4.41 ng/ml; n=22) than in those without LN (5.39±1.54 ng/ml; n=28) (p=0.000). Urinary lipocalin-2 of patients with LN correlated significantly with the renal SLEDAI score (r=0.790, p=0.000), but not with extrarenal disease activity. Within follow up group, urinary lipocalin-2 levels showed significant difference when compared between with and without LN groups (p =0.016). Change in total and renal SLEDAI scores were associated with change of urinary lipocalin-2 levels within follow up group but none of these changes reached statistical significance.ConclusionsUrinary lipocalin-2 is a potential biomarker for renal disease activity in adult SLE patients and its serial measurements may be valuable in predict worsening of SLE disease activity.ReferencesBastian HM, Alarcon GS, Roseman JM, McGwin G Jr, Vila LM, Fessler BJ, Reveille JD. Systemic lupus erythematosus in a multi-ethnic US cohort (LUMINA) XLII: Factors predictive of new or worsening proteinuria. Rheumatology 2007; 46:683–9Ho A, Barr SG, Magder LS, Petri M. A decrease in complement is associated with increased renal and hematologic activity in patients with systemic lupus erythematosus. Arthritis Rheum 2001; 44:2350–2357Bolignano D, Donato V, Coppolino G, Campo S, Buemi A, Lacquaniti A, Beumi M. Neutrophil gelatinase-associated lipocalin (NGAL) as a marker of kidney damage, American Journal of Kidney Diseases 2008; vol. 52, no. 3, 595–605Rubinstein T, Pitashny M and Putterman C. The novel role of neutrophil gelatinase-B associated lipocalin (NGAL)/ Lipocalin-2 as a biomarker for lupus nephritis. Autoimmunity Reviews vol 7 2008; no. 3, 229–234Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkM9OwzAMhyMEEmPwDpF27ojXLmnhNMZfaQLEtnPkpq6WsbUlaUGTOHDhRXkSOsaBKyfL1u-z7I-xHog-QChPsSjcgpp1Zn0wEDAMqFmh60OsYI91IJJxO5Zin3WEEGEQJVIdsiPvl20rYog77H06mokIwq-Pz7mzBboNn9iqNLiyRTDg6DnyC1uu0T2T42XOn6jAFb-0ntATH5navtp6w23BH7G2VNSev9l6wSdN1Xh-T9XC2dr6Mz7ij670FW0J4tO6yTbH7CDHlaeT39pl8-ur2fg2mDzc3I1HkyCFgYIAMVPDBBSKDGRmUilVlopEygQoT0GkuRxmaUpKUGIiaaIojEyS5WgIUZlh2GW93d7KlS8N-Vovy8a1f3gNiQClQoihTZ3vUqa90zvKdeVs-_hGg9Bb3fqPbr3VrX90663ulpY7Ol0v_wV-A4FAjbg</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Gamal, N. M.</creator><creator>Mustafa, N.M.</creator><creator>Abda, E. 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A.M.</creatorcontrib><creatorcontrib>Afifi, O.</creatorcontrib><creatorcontrib>Fathi, N.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gamal, N. M.</au><au>Mustafa, N.M.</au><au>Abda, E. A.M.</au><au>Afifi, O.</au><au>Fathi, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SAT0413 Urinary Lipocalin-2 as a Biomarker of Renal Disease Activity in Patients with Lupus Nephritis: A Prospective Study</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2015-06</date><risdate>2015</risdate><volume>74</volume><issue>Suppl 2</issue><spage>808</spage><epage>809</epage><pages>808-809</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundLupus nephritis (LN) is a common manifestation among patients with systemic lupus erythematosus (SLE), occurring in over 50%. One major determinant of poor prognosis among patients with SLE is renal involvement (1). Available renal biomarkers that measure the degree of SLE renal disease activity are too insensitive to allow for early identification of patients with active SLE nephritis, prohibiting early initiation of therapy to avoid permanent renal damage (2). Lipocalin-2 was regarded a novel biomarker in various types of acute kidney injury and chronic kidney diseases (3,4).ObjectivesThe aim of this study was to detect the levels of urinary lipocalin-2 excretion in SLE patients, to determine its association with SLE disease activity focusing on nephritis and to assess its value in predicting changes of SLE disease activity.MethodsThe study included 50 adult SLE patients met 1997 revised ACR classification criteria for SLE and 20 matched healthy controls. Patients were clinically and laboratory evaluated. Activity was assessed using SLEDAI score. SLE patients were classified into 2 groups (with LN and without LN) based on renal parameters of SLEDAI score. Urinary lipocalin-2 levels were measured using ELISA in SLE patients and controls. Twenty five of included patients were enrolled in a longitudinal study one year after the initial visit. SLEDAI score, laboratory investigation and urinary lipocalin-2 levels were assessed and compared with their initial values.ResultsUrinary lipocalin-2 levels were significantly higher in SLE patients (13.2±2.44 ng/ml) compared with normal controls (1.70±0.23 ng/ml) (p=0.004). Among SLE patients, urinary lipocalin-2 levels were significantly higher in patients with LN (22.95±4.41 ng/ml; n=22) than in those without LN (5.39±1.54 ng/ml; n=28) (p=0.000). Urinary lipocalin-2 of patients with LN correlated significantly with the renal SLEDAI score (r=0.790, p=0.000), but not with extrarenal disease activity. Within follow up group, urinary lipocalin-2 levels showed significant difference when compared between with and without LN groups (p =0.016). Change in total and renal SLEDAI scores were associated with change of urinary lipocalin-2 levels within follow up group but none of these changes reached statistical significance.ConclusionsUrinary lipocalin-2 is a potential biomarker for renal disease activity in adult SLE patients and its serial measurements may be valuable in predict worsening of SLE disease activity.ReferencesBastian HM, Alarcon GS, Roseman JM, McGwin G Jr, Vila LM, Fessler BJ, Reveille JD. Systemic lupus erythematosus in a multi-ethnic US cohort (LUMINA) XLII: Factors predictive of new or worsening proteinuria. Rheumatology 2007; 46:683–9Ho A, Barr SG, Magder LS, Petri M. A decrease in complement is associated with increased renal and hematologic activity in patients with systemic lupus erythematosus. Arthritis Rheum 2001; 44:2350–2357Bolignano D, Donato V, Coppolino G, Campo S, Buemi A, Lacquaniti A, Beumi M. Neutrophil gelatinase-associated lipocalin (NGAL) as a marker of kidney damage, American Journal of Kidney Diseases 2008; vol. 52, no. 3, 595–605Rubinstein T, Pitashny M and Putterman C. The novel role of neutrophil gelatinase-B associated lipocalin (NGAL)/ Lipocalin-2 as a biomarker for lupus nephritis. Autoimmunity Reviews vol 7 2008; no. 3, 229–234Disclosure of InterestNone declared</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2015-eular.1871</doi><tpages>2</tpages></addata></record>
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