Total Cell-Free DNA Predicts Death and Infection Following Pediatric and Adult Heart Transplantation

• Published in: The Annals of thoracic surgery Vol. 112; no. 4; pp. 1282 - 1289
• Main Authors: Scott, John P., Ragalie, William S., Stamm, Karl D., Mahnke, Donna K., Liang, Huan ling, Simpson, Pippa M., Dasgupta, Mahua, Katz, Ronit, North, Paula E., Tomita-Mitchell, Aoy, Zangwill, Steven D., Kindel, Steven J., Mitchell, Michael E.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.10.2021
• Subjects: DF; cfDNA; CI; TCF; TFI; CAV; OHT; EMB; IQR
• ISSN: 0003-4975; 1552-6259
• DOI: 10.1016/j.athoracsur.2020.08.006

Elevated total cell-free DNA (TCF) concentration has been associated with critical illness in adults and elevated donor fraction (DF), the ratio of donor specific cell-free DNA to total cell-free DNA present in the recipient’s plasma, is associated with rejection following cardiac transplantation. This study investigates relationships between TCF and clinical outcomes after heart transplantation. A prospective, blinded, observational study of 87 heart transplantation recipients was performed. Samples were collected at transplantation, prior to endomyocardial biopsy, during treatment for rejection, and at hospital readmissions. Longitudinal clinical data were collected and entered into a RedCAP (Vanderbilt University) database. TCF and DF levels were correlated with endomyocardial biopsy and angiography results, as well as clinical outcomes. Logistic regression for modeling and repeated measures analysis using generalized linear modeling was used. The standard receiver operating characteristic curve, hazard ratios, and odds ratios were calculated. There were 257 samples from 87 recipients analyzed. TCF greater than 50 ng/mL were associated with increased mortality (P = .01, area under the curve 0.93, sensitivity 0.44, specificity 0.97) and treatment for infection (P < .005, area under the curve 0.68, sensitivity 0.45, specificity 0.96). Increased DF was not correlated with treatment for infection. DF was associated with rejection and cardiac allograft vasculopathy (P < .001), but TCF was not. TCF elevation predicted death and treatment for infection. DF elevation predicted histopathologic acute rejection and cardiac allograft vasculopathy. Surveillance of TCF and DF levels may inform treatment after heart transplantation.