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Published on: May 7, 2019
Recurrent IgA Nephropathy After Kidney Transplantation
S Nijim1, V Vujjini1, S Alasfar1
1Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Recurrence of Immunoglobulin A (IgA) nephropathy after kidney transplant significantly reduces allograft survival. Younger recipients and living related donors are linked to higher IgA recurrence rates.
Area of Science:
- Nephrology
- Transplantation Immunology
- Glomerular Diseases
Background:
- Immunoglobulin A (IgA) nephropathy is a leading cause of kidney disease globally.
- High rates of IgA nephropathy recurrence post-kidney transplantation pose a significant clinical challenge.
- Understanding recurrence factors is vital for improving long-term transplant outcomes.
Purpose of the Study:
- To evaluate the survival of kidney allografts in patients with IgA nephropathy.
- To determine the impact of IgA recurrence on allograft function and survival.
- To identify risk factors associated with IgA nephropathy recurrence after transplantation.
Main Methods:
- Retrospective analysis of 104 kidney transplant recipients with IgA nephropathy between 1993 and 2014.
- Inclusion of patients who underwent single or multiple allografts.
- Documentation and analysis of IgA recurrence events and associated clinical data.
Main Results:
- IgA nephropathy recurrence was observed in 19% of allografts, with a median time to recurrence of 6.75 years.
- Younger age at transplantation (mean 37.7 years) and living related donors were associated with increased recurrence risk.
- Allograft survival was significantly reduced in patients with recurrence (6.5 years) versus those without (10.4 years).
- At 6 years post-transplant, 52% of the recurrence group experienced allograft failure compared to 10% in the non-recurrence group.
Conclusions:
- Post-transplant IgA nephropathy recurrence is a major contributor to kidney allograft loss.
- Younger recipient age and the use of living related donors are significant risk factors for recurrence.
- Intensified monitoring and timely treatment are essential for managing IgA recurrence and preserving allograft function.
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