Source:http://linkedlifedata.com/resource/pubmed/id/16528543
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2006-5-16
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pubmed:abstractText |
Acute kidney injury secondary to ischemia-reperfusion in renal allografts often results in delayed graft function. We tested the hypothesis that expression of neutrophil gelatinase-associated lipocalin (NGAL) is an early marker of acute kidney injury following transplantation. Sections from paraffin-embedded protocol biopsy specimens obtained at approximately one hour of reperfusion after transplantation of 13 cadaveric (CAD) and 12 living-related (LRD) renal allografts were examined by immunohistochemistry for expression of NGAL. The staining intensity was correlated with cold ischemia time, peak post-operative serum creatinine, and dialysis requirement. There were no differences between the LRD and CAD groups in age, gender or preoperative serum creatinine. Using a scoring system of 0 (no staining) to 3 (most intense staining), NGAL expression was significantly increased in CAD specimens (2.3+/-0.8 versus 0.8+/-0.7 in LRD, p<0.001). There was a strong correlation between NGAL staining intensity and cold ischemia time (R=0.87, p<0.001). Importantly, NGAL staining in these early CAD biopsies was strongly correlated with peak postoperative serum creatinine, which occurred days later (R=0.86, p<0.001). Four patients developed delayed graft function requiring dialysis during the first week posttransplantation; all of these patients displayed the most intense NGAL staining in their first protocol biopsies. We conclude that NGAL staining intensity in early protocol biopsies represents a novel predictive biomarker of acute kidney injury following transplantation.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/DK-58872,
http://linkedlifedata.com/resource/pubmed/grant/P50-DK52612,
http://linkedlifedata.com/resource/pubmed/grant/R01-DK53289,
http://linkedlifedata.com/resource/pubmed/grant/R01-DK55388,
http://linkedlifedata.com/resource/pubmed/grant/R21-DK070163
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acute-Phase Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/LCN2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Lipocalins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0931-041X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
856-63
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:16528543-Acute Kidney Injury,
pubmed-meshheading:16528543-Acute-Phase Proteins,
pubmed-meshheading:16528543-Adolescent,
pubmed-meshheading:16528543-Adult,
pubmed-meshheading:16528543-Biological Markers,
pubmed-meshheading:16528543-Cadaver,
pubmed-meshheading:16528543-Child,
pubmed-meshheading:16528543-Delayed Graft Function,
pubmed-meshheading:16528543-Female,
pubmed-meshheading:16528543-Humans,
pubmed-meshheading:16528543-Kidney,
pubmed-meshheading:16528543-Kidney Transplantation,
pubmed-meshheading:16528543-Lipocalins,
pubmed-meshheading:16528543-Living Donors,
pubmed-meshheading:16528543-Male,
pubmed-meshheading:16528543-Prognosis,
pubmed-meshheading:16528543-Proto-Oncogene Proteins,
pubmed-meshheading:16528543-Reperfusion Injury,
pubmed-meshheading:16528543-Tissue Donors
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pubmed:year |
2006
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pubmed:articleTitle |
Kidney NGAL is a novel early marker of acute injury following transplantation.
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pubmed:affiliation |
Nephrology and Hypertension, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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