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dc.contributor.authorAnfaiha-Sánchez, Miriames_ES
dc.contributor.authorRodrigo Calabia, Emilio es_ES
dc.contributor.authorOrtiz, Albertoes_ES
dc.contributor.authorMartín-Lorenzo, Martaes_ES
dc.contributor.authorÁlvarez-Llamas, Gloriaes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-09-27T15:26:37Z
dc.date.available2023-09-27T15:26:37Z
dc.date.issued2023es_ES
dc.identifier.issn2048-8505es_ES
dc.identifier.issn2048-8513es_ES
dc.identifier.urihttps://hdl.handle.net/10902/30014
dc.description.abstractKidney transplantation is the treatment of choice for patients with kidney failure. Priority on the waiting list and optimal donor–recipient matching are guided by mathematical scores, clinical variables and macroscopic observation of the donated organ. Despite the increasing rates of successful kidney transplantation, maximizing the number of available organs while ensuring the optimum long-term performance of the transplanted kidney remains both key and challenging, and no unequivocal markers are available for clinical decision making. Moreover, the majority of studies performed thus far has focused on the risk of primary non-function and delayed graft function and subsequent survival and have mainly analysed recipients’ samples. Given the increasing use of donors with expanded criteria and/or cardiac death, predicting whether grafts will provide sufficient kidney function is increasingly more challenging. Here we compile the available tools for pre-transplant kidney evaluation and summarize the latest molecular data from donors that may predict short-term (immediate or delayed graft function), medium-term (6 months) and long-term (≥12 months) kidney function. The use of liquid biopsy (urine, serum, plasma) to overcome the limitations of the pre transplant histological evaluation is proposed. Novel molecules and approaches such as the use of urinary extracellular vesicles are also reviewed and discussed, along with directions for future researches_ES
dc.description.sponsorshipFunding: This work was supported by Fundación Mutua Madrileña, Instituto de Salud Carlos III (RICORS2040-RD21/0005/0001) FEDER funds, Fundación SENEFRO/SEN and Comunidad Autónoma de Madrid (CAM) (2018-T2/BMD-11561, PEJD-2020-AI/BMD-17899)es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsAttribution-NonCommercial 4.0 International*
dc.rights© The Author(s) 2022es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.sourceClinical Kidney Journal, 2023, 16,(3), 447-455es_ES
dc.subject.otherAcute kidney injuryes_ES
dc.subject.otherBiomarkerses_ES
dc.subject.otherChronic kidney diseasees_ES
dc.subject.otherDelayed graft functiones_ES
dc.subject.otherDonores_ES
dc.subject.otherExtracellular vesicleses_ES
dc.titleDonor liquid biopsy and outcomes in kidney transplantationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1093/ckj/sfac227es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/ckj/sfac227es_ES
dc.type.versionpublishedVersiones_ES


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Attribution-NonCommercial 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial 4.0 International