Characterizing Early Donor‐Derived
cfDNA
Kinetics in Stable Pediatric Living‐Donor Liver Transplant Recipients
Naresh Shanmugam, Avinash Ramani, Bhavani Gunasekaran, Pavan Kumar K. Bapatla, Nivethitha Jayakanthan, Ebila Yesudhasan, Mohanty Rithika, Agragesh Ramani, Anu Vasudevan, V. R. Jagadeesh Menon, Ashwin Rammohan, Mohamed Rela ABSTRACT
Background
Early and precise assessment of graft health is vital for pediatric liver transplant patients; however, current monitoring methods depend largely on invasive biopsies and non‐specific biochemical tests. Donor‐derived cell‐free DNA (ddcfDNA) has emerged as a promising non‐invasive biomarker for detecting graft injury, but data on its early post‐transplant kinetics, baseline levels, and the influence of donor and recipient factors in stable pediatric populations remain limited.
Objective
To prospectively characterize the early postoperative patterns of ddcfDNA and explore baseline ranges in clinically stable pediatric recipients of living donor liver transplants (LDLT), while evaluating the influence of recipient and donor demographic and clinical variables on ddcfDNA dynamics for improved non‐invasive graft monitoring.
Methods
In a cohort of 22 stable pediatric LDLT recipients, ddcfDNA levels were measured longitudinally using the Trunome GrafAssure assay at postoperative days 1–2, 7, 10–14, and 30–31. Concurrent liver function tests and clinical data were also collected. Statistical analyses were performed to evaluate correlations and determine the significance of the observed relationships.
Results
ddcfDNA peaked on days 1–2 (~9.0%, 2.3 ng/mL), declined sharply by day 7 (~2.4%, 1.0 ng/mL), and stabilized by days 30–31 (~2.0%, 0.2 ng/mL). Liver enzymes decreased gradually. The absolute quantification values and the ddcfDNA percentage correlated with AST and ALT early post‐transplant, with associations diminishing over time. Recipient and donor characteristics did not significantly affect ddcfDNA levels.
Conclusion
dd‐cfDNA demonstrates rapid postoperative clearance and stable longitudinal trends in clinically stable pediatric liver transplant recipients. The baseline values and kinetic patterns characterized provide a preliminary reference framework for future comparative studies evaluating dd‐cfDNA behavior during graft dysfunction, rejection, or other adverse events in the early postoperative and surveillance periods.