DNA damage in kidney transplant patients. Role of organ origin

Zuray Corredor1, Lara Rodríguez-Ribera1, Elisabet Coll2

  • 1Grup de Mutagènesi, Departament de Genètica i de Microbiologia, Edifici C, Universitat Autònoma de Barcelona, Bellaterra, Cerdanyola del Vallès, 08193, Spain.

Insights

Kidney transplant recipients showed increased genomic damage post-transplant, despite improved kidney function. Living donor transplants had lower DNA damage than cadaveric donor transplants, indicating donor age and type impact genomic health.

Area of Science:

  • Genomic damage and DNA repair
  • Nephrology and transplantation science
  • Biomarkers of cellular damage

Background:

  • Chronic kidney disease (CKD) is associated with elevated genomic damage, worsening with reduced kidney function.
  • Hemodialysis patients exhibit maximum levels of genomic damage.
  • Kidney transplantation improves renal function and patient survival.

Purpose of the Study:

  • To evaluate changes in DNA damage levels following kidney transplantation.
  • To compare DNA damage in living donor versus cadaveric donor recipients.
  • To assess the relationship between renal function improvement and genomic damage post-transplant.

Main Methods:

  • Utilized the alkaline comet assay to quantify DNA breaks and oxidative DNA damage.
  • Employed the micronucleus assay to detect chromosomal breakage and aneuploidy.
  • Monitored 50 CKD patients at 6 and 12 months post-kidney transplantation.

Main Results:

  • All patients exhibited increased genomic damage levels at 6 and 12 months post-transplantation compared to pre-transplant levels.
  • Despite improved metabolic functions, DNA damage increased after transplantation.
  • Advanced donor age positively correlated with higher DNA damage.
  • Genomic damage was significantly lower in living donor transplants compared to cadaveric donor transplants.

Conclusions:

  • Kidney transplantation leads to an increase in DNA damage, even with improved renal function.
  • Cadaveric donor transplants are associated with higher levels of genomic damage than living donor transplants.
  • Donor characteristics, such as age and type, influence post-transplant genomic damage levels.

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