scholarly journals FACTORS PREDICTING POOR GRAFT FUNCTION AT 1 YEAR AFTER KIDNEY TRANSPLANTATION FROM DECEASED DONORS WITH ACUTE KIDNEY INJURY: AN ANALYSIS OF KOREAN ORGAN TRANSPLANT REGISTRY DATABASE

2020 ◽  
Vol 104 (S3) ◽  
pp. S343-S343
Author(s):  
Jane Ha ◽  
Cheol Woong Jung ◽  
Joong Kyung Kim ◽  
Chan-Duck Kim ◽  
Ji Won Min ◽  
...  
PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10441
Author(s):  
Hui Bi ◽  
Min Zhang ◽  
Jialin Wang ◽  
Gang Long

Background This study aims to identify potential biomarkers associated with acute kidney injury (AKI) post kidney transplantation. Material and Methods Two mRNA expression profiles from Gene Expression Omnibus repertory were downloaded, including 20 delayed graft function (DGF) and 68 immediate graft function (IGF) samples. Differentially expressed genes (DEGs) were identified between DGF and IGF group. The Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis of DEGs were performed. Then, a protein-protein interaction analysis was performed to extract hub genes. The key genes were searched by literature retrieval and cross-validated based on the training dataset. An external dataset was used to validate the expression levels of key genes. Receiver operating characteristic curve analyses were performed to evaluate diagnostic performance of key genes for AKI. Results A total of 330 DEGs were identified between DGF and IGF samples, including 179 up-regulated and 151 down-regulated genes. Of these, OLIG3, EBF3 and ETV1 were transcription factor genes. Moreover, LEP, EIF4A3, WDR3, MC4R, PPP2CB, DDX21 and GPT served as hub genes in PPI network. EBF3 was significantly up-regulated in validation GSE139061 dataset, which was consistently with our initial gene differential expression analysis. Finally, we found that LEP had a great diagnostic value for AKI (AUC = 0.740). Conclusion EBF3 may be associated with the development of AKI following kidney transplantation. Furthermore, LEP had a good diagnostic value for AKI. These findings provide deeper insights into the diagnosis and management of AKI post renal transplantation.


2019 ◽  
Vol 51 (8) ◽  
pp. 2575-2581 ◽  
Author(s):  
Jin Ah Kwon ◽  
Hojong Park ◽  
Sang Jun Park ◽  
Hong Rae Cho ◽  
Minsu Noh ◽  
...  

2019 ◽  
Vol 34 (Supplement_1) ◽  
Author(s):  
Reinis Lulle ◽  
Gritane Klinta ◽  
Asare Lasma ◽  
Jushinskis Janis ◽  
Malcevs Aleksandrs ◽  
...  

2010 ◽  
Vol 90 ◽  
pp. 195
Author(s):  
N. Techawathanawanna ◽  
R. Kunprakan ◽  
P. Lertsithichai ◽  
K. Pipatpannawong ◽  
N. Naitook ◽  
...  

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Jolanta Malyszko ◽  
Ewelina Lukaszyk ◽  
Irena Glowinska ◽  
Magdalena Durlik

PLoS ONE ◽  
2021 ◽  
Vol 16 (3) ◽  
pp. e0249000
Author(s):  
Juan Pei ◽  
Yeoungjee Cho ◽  
Yong Pey See ◽  
Elaine M. Pascoe ◽  
Andrea K. Viecelli ◽  
...  

Background The need for kidney transplantation drives efforts to expand organ donation. The decision to accept organs from donors with acute kidney injury (AKI) can result in a clinical dilemma in the context of conflicting reports from published literature. Material and methods This observational study included all deceased donor kidney transplants performed in Australia and New Zealand between 1997 and 2017. The association of donor-AKI, defined according to KDIGO criteria, with all-cause graft failure was evaluated by multivariable Cox regression. Secondary outcomes included death-censored graft failure, death, delayed graft function (DGF) and acute rejection. Results The study included 10,101 recipients of kidneys from 5,774 deceased donors, of whom 1182 (12%) recipients received kidneys from 662 (11%) donors with AKI. There were 3,259 (32%) all-cause graft failures, which included 1,509 deaths with functioning graft. After adjustment for donor, recipient and transplant characteristics, donor AKI was not associated with all-cause graft failure (adjusted hazard ratio [HR] 1.11, 95% CI 0.99–1.26), death-censored graft failure (HR 1.09, 95% CI 0.92–1.28), death (HR 1.15, 95% CI 0.98–1.35) or graft failure when death was evaluated as a competing event (sub-distribution hazard ratio [sHR] 1.07, 95% CI 0.91–1.26). Donor AKI was not associated with acute rejection but was associated with DGF (adjusted odds ratio [OR] 2.27, 95% CI 1.92–2.68). Conclusion Donor AKI stage was not associated with any kidney transplant outcome, except DGF. Use of kidneys with AKI for transplantation appears to be justified.


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