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Urine liver-type fatty acid-binding protein predicts graft outcome up to 2 years after kidney transplantation

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dc.contributor.authorYang, J.-
dc.contributor.authorChoi, H. M.-
dc.contributor.authorSeo, M. Y.-
dc.contributor.authorLee, J. Y.-
dc.contributor.authorKim, K.-
dc.contributor.authorJun, H.-
dc.contributor.authorJung, C. W.-
dc.contributor.authorPark, K. T.-
dc.contributor.authorKim, M. -G.-
dc.contributor.authorJo, S. -K.-
dc.contributor.authorCho, W.-
dc.contributor.authorKim, H. K.-
dc.date.accessioned2022-07-16T05:33:05Z-
dc.date.available2022-07-16T05:33:05Z-
dc.date.created2021-05-13-
dc.date.issued2014-03-
dc.identifier.issn0041-1345-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160398-
dc.description.abstractBackground Several new biomarkers for the detection of early tubular injury have been investigated in kidney transplant recipients. We recently identified day 2 urinary neutrophil gelatinase-associated lipocalin (NGAL) as a predictor of slow graft function and adverse 1-year outcome. In the present study, we further investigated the value of urinary NGAL and liver-type fatty acid binding protein (L-FABP) for predicting long-term graft outcomes up to 2 years. Methods This study was a single-center, prospective observational study. Serial urinary NGAL and L-FABP levels at 0 hours, 2 days, and 6 days after kidney transplantation (KT) were measured, and the clinical data were assessed during the 2-year period after KT. Results During the 2-year follow-up period, 13 (18.8%), 5 (7.2%), and 4 (5.8%) patients were diagnosed with acute T-cell-mediated rejection, acute antibody-mediated rejection (AMR) and chronic AMR, respectively. In addition, 10 patients (14.3%) developed calcineurin inhibitor toxicity and 6 (8.7%) developed BK viremia. The mean estimated glomerular filtration rates (eGFR) at 1 and 2 years after KT were 65.1 ± 19.1 and 58.5 ± 22.6 mL/min/1.73 m2, respectively, When poor long-term graft function was defined as eGFR of less than 50 mL/min/1.73 m 2 at 2 years, elderly donors, acute rejection, and high 0-hour urinary L-FABP levels were significant risk factors. Furthermore, in rejection-free patients, L-FABP was strongly associated with poor long-term graft function (P =.006). Multivariate logistic regression analysis showed that high 0-hour L-FABP (P =.015) and acute rejection (P =.006) were independent factors predicting poor long-term graft function. Receiver operating characteristic analysis showed that the area under the curve for urinary L-FABP was 0.692 (P =.036). Conclusions Our results suggest that urinary L-FABP may be a useful predictor of adverse long-term outcomes in KT patients.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE INC-
dc.titleUrine liver-type fatty acid-binding protein predicts graft outcome up to 2 years after kidney transplantation-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, H. M.-
dc.identifier.doi10.1016/j.transproceed.2013.11.130-
dc.identifier.scopusid2-s2.0-84896441603-
dc.identifier.wosid000333572100019-
dc.identifier.bibliographicCitationTRANSPLANTATION PROCEEDINGS, v.46, no.2, pp.376 - 380-
dc.relation.isPartOfTRANSPLANTATION PROCEEDINGS-
dc.citation.titleTRANSPLANTATION PROCEEDINGS-
dc.citation.volume46-
dc.citation.number2-
dc.citation.startPage376-
dc.citation.endPage380-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaSurgery-
dc.relation.journalResearchAreaTransplantation-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategorySurgery-
dc.relation.journalWebOfScienceCategoryTransplantation-
dc.subject.keywordPlusGELATINASE-ASSOCIATED LIPOCALIN-
dc.subject.keywordPlusACUTE ISCHEMIC-INJURY-
dc.subject.keywordPlusRENAL-TRANSPLANTATION-
dc.subject.keywordPlusADVERSE OUTCOMES-
dc.subject.keywordPlusCARDIAC-SURGERY-
dc.subject.keywordPlusBIOMARKER-
dc.subject.keywordPlusNGAL-
dc.subject.keywordPlusNEPHROPATHY-
dc.subject.keywordPlusDIALYSIS-
dc.subject.keywordPlusDISEASE-
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