| Literature DB >> 30312536 |
John B Whitlam1,2,3, Ling Ling2, Alison Skene4, John Kanellis5, Francseco L Ierino3,6, Howard R Slater2,7, Damien L Bruno8, David A Power1,3.
Abstract
Graft-derived cell-free DNA (donor-derived cell-free DNA) is an emerging marker of kidney allograft injury. Studies examining the clinical validity of this biomarker have previously used the graft fraction, or proportion of total cell-free DNA that is graft-derived. The present study evaluated the diagnostic validity of absolute measurements of graft-derived cell-free DNA, as well as calculated graft fraction, for the diagnosis of graft dysfunction. Plasma graft-derived cell-free DNA, total cell-free DNA, and graft fraction were correlated with biopsy diagnosis as well as individual Banff scores. Sixty-one samples were included in the analysis. For the diagnosis of antibody mediated rejection, the receiver-operator characteristic area under the curves of graft-derived cell-free DNA and graft fraction were 0.91 (95% CI 0.82-0.98) and 0.89 (95% CI 0.79-0.98), respectively. Both measures did not diagnose borderline or type 1A cellular mediated rejection. Graft fraction was associated with a broader range of Banff lesions, including lesions associated with cellular mediated rejection, while graft-derived cell-free DNA appeared more specific for antibody mediated rejection. Limitations of this study include a small sample size and lack of a validation cohort. The capacity for absolute quantification, and lower barriers to implementation of this methodology recommend it for further study.Entities:
Keywords: biomarker; clinical research/practice; diagnostic techniques and imaging; genetics; kidney (allograft) function/dysfunction; kidney transplantation/nephrology; organ transplantation in general; rejection; rejection: antibody-mediated (ABMR); translational research/science
Year: 2018 PMID: 30312536 DOI: 10.1111/ajt.15142
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086