What is the role of cell-free DNA (cfDNA) in simultaneous kidney and pancreas transplantation?

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Last updated: March 31, 2025View editorial policy

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From the Research

Donor-derived cell-free DNA (dd-cfDNA) is a promising non-invasive biomarker for monitoring organ rejection in simultaneous kidney-pancreas transplant (SKPT) recipients, with levels above 1% suggesting rejection requiring further evaluation, as supported by the most recent study 1.

Key Findings

  • dd-cfDNA levels can detect subclinical rejection earlier than conventional markers, allowing for prompt intervention with immunosuppressive therapy adjustments before permanent graft damage occurs 2.
  • The test is typically performed monthly for the first year post-transplant, then quarterly thereafter, with more frequent testing during suspected rejection episodes.
  • AlloSure values below 1% generally indicate stable graft function, while levels above 1% may suggest rejection requiring further evaluation 1.
  • dd-cfDNA measurement can help differentiate rejection from graft injury, such as pancreatitis, with median values in rejection being significantly higher than in quiescence 2.

Clinical Implications

  • cfDNA monitoring represents an important advancement in transplant care by providing real-time insight into graft health with minimal patient burden.
  • Interpretation of dd-cfDNA levels should consider that values may be temporarily elevated during infections or other inflammatory conditions, and the test cannot always distinguish between kidney and pancreas rejection in SKPT recipients.
  • The use of dd-cfDNA in combination with other non-invasive biomarkers, such as donor-specific antibodies, may provide a more comprehensive assessment of allograft health 3.

Limitations

  • The test cannot always distinguish between kidney and pancreas rejection in SKPT recipients.
  • Values may be temporarily elevated during infections or other inflammatory conditions.
  • Further studies are needed to define the optimal cutoff values for dd-cfDNA and to determine the clinical benefit of routine prospective monitoring in SKPT recipients.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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