Post-transplant nuclear renal scans correlate with renal injury biomarkers and early allograft outcomes

Background. Clinical- and histopathology-based scores are limited predictors of allograft outcome. In addition, more objective markers of early transplant function are needed to identify and validate biomarkers and predictive scores. We evaluated existing scores and transcriptome biomarkers of kidne...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2011-09, Vol.26 (9), p.3038-3045
Hauptverfasser: Obeidat, Motaz A., Luyckx, Valerie A., Grebe, Scott O., Jhangri, Gian S., Maguire, Connor, Zavodni, Anna, Jackson, Stuart, Mueller, Thomas F.
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container_issue 9
container_start_page 3038
container_title Nephrology, dialysis, transplantation
container_volume 26
creator Obeidat, Motaz A.
Luyckx, Valerie A.
Grebe, Scott O.
Jhangri, Gian S.
Maguire, Connor
Zavodni, Anna
Jackson, Stuart
Mueller, Thomas F.
description Background. Clinical- and histopathology-based scores are limited predictors of allograft outcome. In addition, more objective markers of early transplant function are needed to identify and validate biomarkers and predictive scores. We evaluated existing scores and transcriptome biomarkers of kidney injury as predictors of early transplant function measured by renal scan. Methods. Clinical, histopathologic and transcriptome data were collected in 143 consecutive kidney transplant recipients. A post-operative renal scan was performed within 48 h. Prediction scores for early outcomes were calculated. Results. Patients were stratified into three groups by renal scan: normal, mild-to-moderate or severe dysfunction. Kidneys with severe dysfunction were more often from deceased donors (P 
doi_str_mv 10.1093/ndt/gfq814
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Clinical- and histopathology-based scores are limited predictors of allograft outcome. In addition, more objective markers of early transplant function are needed to identify and validate biomarkers and predictive scores. We evaluated existing scores and transcriptome biomarkers of kidney injury as predictors of early transplant function measured by renal scan. Methods. Clinical, histopathologic and transcriptome data were collected in 143 consecutive kidney transplant recipients. A post-operative renal scan was performed within 48 h. Prediction scores for early outcomes were calculated. Results. Patients were stratified into three groups by renal scan: normal, mild-to-moderate or severe dysfunction. Kidneys with severe dysfunction were more often from deceased donors (P < 0.001), had greater HLA antigen mismatches (P < 0.001), were transplanted into older recipients (P = 0.040), had lower urine output during the first 8 h (P < 0.001), higher Day 7 serum creatinine (P < 0.001) and higher incidence of delayed graft function (P < 0.001). Clinical- and pathology-based scores did not discriminate between scan groups. In contrast, the overall transcriptome (P < 0.001) and transcripts of preselected acute kidney injury (AKI) genes were significantly different between the groups, with kidney injury molecule 1 (P = 0.001) and neutrophil gelatinase-associated lipocalin (P = 0.002) being most highly expressed and genes associated with glutathione metabolism (GSTA1, 3 and 4) most down-regulated in kidneys with subsequent severe dysfunction. Conclusions. Renal scans reflect early transplant function and allow for a more objective assessment of scores predicting early outcome and for identification of biomarkers. The study shows that transcript levels of AKI genes correlate better with renal scans than clinical- or histopathology-based scores.]]></description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfq814</identifier><identifier>PMID: 21321005</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Acute Kidney Injury - diagnosis ; Acute Kidney Injury - etiology ; Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Biomarkers - analysis ; Biomarkers - metabolism ; Delayed Graft Function - diagnosis ; Delayed Graft Function - etiology ; Emergency and intensive care: renal failure. Dialysis management ; Female ; Follow-Up Studies ; Gene Expression Profiling ; Graft Rejection - diagnosis ; Graft Rejection - etiology ; Humans ; Intensive care medicine ; Kidney - physiopathology ; Kidney Transplantation ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Oligonucleotide Array Sequence Analysis ; Prognosis ; RNA, Messenger - genetics ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Survival Rate ; Transplantation, Homologous</subject><ispartof>Nephrology, dialysis, transplantation, 2011-09, Vol.26 (9), p.3038-3045</ispartof><rights>The Author 2011. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-afbae2c299a19311d8d8c6566ccfb34dfdd90cb7c0b1c2480acde9a6ccfd0c643</citedby><cites>FETCH-LOGICAL-c382t-afbae2c299a19311d8d8c6566ccfb34dfdd90cb7c0b1c2480acde9a6ccfd0c643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24565624$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21321005$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Obeidat, Motaz A.</creatorcontrib><creatorcontrib>Luyckx, Valerie A.</creatorcontrib><creatorcontrib>Grebe, Scott O.</creatorcontrib><creatorcontrib>Jhangri, Gian S.</creatorcontrib><creatorcontrib>Maguire, Connor</creatorcontrib><creatorcontrib>Zavodni, Anna</creatorcontrib><creatorcontrib>Jackson, Stuart</creatorcontrib><creatorcontrib>Mueller, Thomas F.</creatorcontrib><title>Post-transplant nuclear renal scans correlate with renal injury biomarkers and early allograft outcomes</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description><![CDATA[Background. Clinical- and histopathology-based scores are limited predictors of allograft outcome. In addition, more objective markers of early transplant function are needed to identify and validate biomarkers and predictive scores. We evaluated existing scores and transcriptome biomarkers of kidney injury as predictors of early transplant function measured by renal scan. Methods. Clinical, histopathologic and transcriptome data were collected in 143 consecutive kidney transplant recipients. A post-operative renal scan was performed within 48 h. Prediction scores for early outcomes were calculated. Results. Patients were stratified into three groups by renal scan: normal, mild-to-moderate or severe dysfunction. Kidneys with severe dysfunction were more often from deceased donors (P < 0.001), had greater HLA antigen mismatches (P < 0.001), were transplanted into older recipients (P = 0.040), had lower urine output during the first 8 h (P < 0.001), higher Day 7 serum creatinine (P < 0.001) and higher incidence of delayed graft function (P < 0.001). Clinical- and pathology-based scores did not discriminate between scan groups. In contrast, the overall transcriptome (P < 0.001) and transcripts of preselected acute kidney injury (AKI) genes were significantly different between the groups, with kidney injury molecule 1 (P = 0.001) and neutrophil gelatinase-associated lipocalin (P = 0.002) being most highly expressed and genes associated with glutathione metabolism (GSTA1, 3 and 4) most down-regulated in kidneys with subsequent severe dysfunction. Conclusions. Renal scans reflect early transplant function and allow for a more objective assessment of scores predicting early outcome and for identification of biomarkers. The study shows that transcript levels of AKI genes correlate better with renal scans than clinical- or histopathology-based scores.]]></description><subject>Acute Kidney Injury - diagnosis</subject><subject>Acute Kidney Injury - etiology</subject><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Biomarkers - metabolism</subject><subject>Delayed Graft Function - diagnosis</subject><subject>Delayed Graft Function - etiology</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gene Expression Profiling</subject><subject>Graft Rejection - diagnosis</subject><subject>Graft Rejection - etiology</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Kidney - physiopathology</subject><subject>Kidney Transplantation</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Prognosis</subject><subject>RNA, Messenger - genetics</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Survival Rate</subject><subject>Transplantation, Homologous</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqWw4QOQNwgJKdR2nl6iipdUCRawjpyxU1KcOLUdof49rhrojpUX98yM70HokpI7Sng876Sfr-pNQZMjNKVJRiIWF-kxmoaQRiQlfILOnFsTQjjL81M0YTRmlJB0ilZvxvnIW9G5XovO424ArYTFVnVCYwchwGCsVVp4hb8b_zlGTbce7BZXjWmF_VLWYdFJHEb1FgutzcqK2mMzeDCtcufopBbaqYvxnaGPx4f3xXO0fH16WdwvI4gL5iNRV0IxYJwLGj5PZSELyNIsA6irOJG1lJxAlQOpKLCkIAKk4mIXSwJZEs_QzX5vb81mUM6XbeNA6dBNmcGVBWc8yTlNA3m7J8Ea56yqy942ocq2pKTceS2D13LvNcBX49qhapX8Q39FBuB6BERwpusgFBp34JI0tGDJgTND_9_BH-YkkWo</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Obeidat, Motaz A.</creator><creator>Luyckx, Valerie A.</creator><creator>Grebe, Scott O.</creator><creator>Jhangri, Gian S.</creator><creator>Maguire, Connor</creator><creator>Zavodni, Anna</creator><creator>Jackson, Stuart</creator><creator>Mueller, Thomas F.</creator><general>Oxford University Press</general><scope>IQODW</scope><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></search><sort><creationdate>20110901</creationdate><title>Post-transplant nuclear renal scans correlate with renal injury biomarkers and early allograft outcomes</title><author>Obeidat, Motaz A. ; Luyckx, Valerie A. ; Grebe, Scott O. ; Jhangri, Gian S. ; Maguire, Connor ; Zavodni, Anna ; Jackson, Stuart ; Mueller, Thomas F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-afbae2c299a19311d8d8c6566ccfb34dfdd90cb7c0b1c2480acde9a6ccfd0c643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acute Kidney Injury - diagnosis</topic><topic>Acute Kidney Injury - etiology</topic><topic>Adult</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Biomarkers - metabolism</topic><topic>Delayed Graft Function - diagnosis</topic><topic>Delayed Graft Function - etiology</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gene Expression Profiling</topic><topic>Graft Rejection - diagnosis</topic><topic>Graft Rejection - etiology</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Kidney - physiopathology</topic><topic>Kidney Transplantation</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Prognosis</topic><topic>RNA, Messenger - genetics</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Survival Rate</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Obeidat, Motaz A.</creatorcontrib><creatorcontrib>Luyckx, Valerie A.</creatorcontrib><creatorcontrib>Grebe, Scott O.</creatorcontrib><creatorcontrib>Jhangri, Gian S.</creatorcontrib><creatorcontrib>Maguire, Connor</creatorcontrib><creatorcontrib>Zavodni, Anna</creatorcontrib><creatorcontrib>Jackson, Stuart</creatorcontrib><creatorcontrib>Mueller, Thomas F.</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Obeidat, Motaz A.</au><au>Luyckx, Valerie A.</au><au>Grebe, Scott O.</au><au>Jhangri, Gian S.</au><au>Maguire, Connor</au><au>Zavodni, Anna</au><au>Jackson, Stuart</au><au>Mueller, Thomas F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Post-transplant nuclear renal scans correlate with renal injury biomarkers and early allograft outcomes</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>26</volume><issue>9</issue><spage>3038</spage><epage>3045</epage><pages>3038-3045</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract><![CDATA[Background. Clinical- and histopathology-based scores are limited predictors of allograft outcome. In addition, more objective markers of early transplant function are needed to identify and validate biomarkers and predictive scores. We evaluated existing scores and transcriptome biomarkers of kidney injury as predictors of early transplant function measured by renal scan. Methods. Clinical, histopathologic and transcriptome data were collected in 143 consecutive kidney transplant recipients. A post-operative renal scan was performed within 48 h. Prediction scores for early outcomes were calculated. Results. Patients were stratified into three groups by renal scan: normal, mild-to-moderate or severe dysfunction. Kidneys with severe dysfunction were more often from deceased donors (P < 0.001), had greater HLA antigen mismatches (P < 0.001), were transplanted into older recipients (P = 0.040), had lower urine output during the first 8 h (P < 0.001), higher Day 7 serum creatinine (P < 0.001) and higher incidence of delayed graft function (P < 0.001). Clinical- and pathology-based scores did not discriminate between scan groups. In contrast, the overall transcriptome (P < 0.001) and transcripts of preselected acute kidney injury (AKI) genes were significantly different between the groups, with kidney injury molecule 1 (P = 0.001) and neutrophil gelatinase-associated lipocalin (P = 0.002) being most highly expressed and genes associated with glutathione metabolism (GSTA1, 3 and 4) most down-regulated in kidneys with subsequent severe dysfunction. Conclusions. Renal scans reflect early transplant function and allow for a more objective assessment of scores predicting early outcome and for identification of biomarkers. The study shows that transcript levels of AKI genes correlate better with renal scans than clinical- or histopathology-based scores.]]></abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21321005</pmid><doi>10.1093/ndt/gfq814</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute Kidney Injury - diagnosis
Acute Kidney Injury - etiology
Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Biomarkers - analysis
Biomarkers - metabolism
Delayed Graft Function - diagnosis
Delayed Graft Function - etiology
Emergency and intensive care: renal failure. Dialysis management
Female
Follow-Up Studies
Gene Expression Profiling
Graft Rejection - diagnosis
Graft Rejection - etiology
Humans
Intensive care medicine
Kidney - physiopathology
Kidney Transplantation
Magnetic Resonance Imaging
Male
Medical sciences
Middle Aged
Oligonucleotide Array Sequence Analysis
Prognosis
RNA, Messenger - genetics
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the urinary system
Survival Rate
Transplantation, Homologous
title Post-transplant nuclear renal scans correlate with renal injury biomarkers and early allograft outcomes
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