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Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction.
Whitlam, John B; Ling, Ling; Skene, Alison; Kanellis, John; Ierino, Francseco L; Slater, Howard R; Bruno, Damien L; Power, David A.
Afiliación
  • Whitlam JB; Department of Nephrology, Austin Health, Melbourne, Victoria, Australia.
  • Ling L; Cyto-molecular Diagnostics Research Melbourne, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Skene A; Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Kanellis J; Cyto-molecular Diagnostics Research Melbourne, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Ierino FL; Department of Anatomical Pathology, Austin Health, Melbourne, Victoria, Australia.
  • Slater HR; Department of Nephrology, Department of Medicine, Monash Health and Centre for Inflammatory Diseases, Monash University, Melbourne, Victoria, Australia.
  • Bruno DL; Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Power DA; Department of Nephrology, St Vincent's Health, Melbourne, Victoria, Australia.
Am J Transplant ; 19(4): 1037-1049, 2019 04.
Article en En | MEDLINE | ID: mdl-30312536
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Ácidos Nucleicos Libres de Células / Rechazo de Injerto Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2019 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Riñón / Ácidos Nucleicos Libres de Células / Rechazo de Injerto Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2019 Tipo del documento: Article País de afiliación: Australia