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Effect of donor source on renal allograft function in children on triple immunosuppression

J Laine1, F Fyhrquist, C Holmberg

  • 1II Department of Pediatrics, University of Helsinki, Finland.

Insights

Kidney transplant outcomes from deceased (CAD) and living related donors (LRD) were compared. CAD grafts showed lower initial function but stabilized, with minimal long-term differences, suggesting donor source has little impact on dysfunction.

Area of Science:

  • Nephrology
  • Transplantation Immunology
  • Pediatric Nephrology

Background:

  • Renal transplantation outcomes typically differ between cadaver (CAD) and living related donors (LRD).
  • Previous studies reported excellent 1-year graft survival for both CAD and LRD using triple immunosuppression.

Purpose of the Study:

  • To compare glomerular and tubular function in pediatric renal grafts from LRD versus CAD donors over 3 years post-transplantation.
  • To assess the long-term impact of donor source on allograft function and dysfunction.

Main Methods:

  • Prospective study comparing 23 LRD and 22 CAD renal grafts in preschool children.
  • Glomerular filtration rate (GFR), renal plasma flow, and tubular function were assessed over 3 years.
  • Serum urate levels and cyclosporine-induced nephrotoxicity markers were monitored.

Main Results:

  • CAD grafts exhibited lower initial GFR and renal plasma flow compared to LRD grafts.
  • Both LRD and CAD graft functions remained stable throughout the 3-year follow-up period.
  • No significant differences in GFR or tubular function were observed after 6 months; however, LRD grafts showed better urate handling at 36 months.

Conclusions:

  • Donor source had minimal impact on the development of progressive allograft dysfunction in pediatric renal transplantation with triple immunosuppression.
  • Cyclosporine-induced nephrotoxicity, including hyperkalemia, was noted.
  • Adult CAD grafts are a viable option for pediatric renal transplantation when using triple immunosuppression.

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