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Published on: October 11, 2014
Study of Glomerulopathy in Donors after Kidney Transplantation
Minako Murata1, Asami Takeda2, Yasuhiro Ootsuka2
1Department of Kidney Disease Center, Nagoya Daini Red Cross Hospital, Nagoya, Japan, minakom@nagoya2.jrc.or.jp.
Insights
Living kidney donors may face risks of kidney disease post-donation. Baseline biopsies and long-term follow-up are crucial for early detection and management of kidney conditions in these individuals.
Area of Science:
- Nephrology
- Transplantation Immunology
- Urology
Background:
- Living kidney donation is a vital treatment for end-stage renal disease.
- Emerging evidence suggests potential long-term renal function decline in living kidney donors.
Purpose of the Study:
- To investigate the clinical and pathological characteristics of living kidney donors who developed kidney disease post-donation.
- To emphasize the importance of baseline renal assessment and ongoing monitoring for living kidney donors.
Main Methods:
- Retrospective analysis of 1,625 living kidney donors from January 1991 to May 2019.
- Detailed review of clinical records and renal biopsy findings for 7 donors who developed kidney disease.
Main Results:
- Identified 7 cases of post-donation kidney disease, including IgA nephropathy (3), membranous nephropathy (2), ANCA-associated glomerulonephritis (1), and secondary FSGS (1).
- Latent IgA deposition was noted in all IgA nephropathy cases; one membranous nephropathy case showed baseline biopsy findings despite being asymptomatic.
- Most patients, excluding those with ANCA-associated nephropathy and secondary FSGS, showed recovery or maintained adequate renal function after treatment.
Conclusions:
- Baseline renal biopsies are essential for evaluating donor kidney health prior to donation.
- Long-term follow-up tailored to baseline biopsy findings is recommended for living kidney donors.
- Prompt diagnosis and treatment are critical for managing kidney disease in living kidney donors.
Introduction:
Living kidney donation improves the lives of individuals with kidney failure; however, recent studies have suggested that living kidney donors may be at a relatively higher risk of reduced renal function than healthy non-donors. We therefore aimed to evaluate the clinical and pathological findings in living kidney donors who developed kidney disease.
Methods:
From January 1991 to May 2019, 1,625 live kidney donations were performed at our hospital. Among the donors, 7 developed kidney disease after donation and underwent open renal biopsy. We studied the clinical and pathological findings of these patients from their clinical records.
Results:
There were 3 patients with immunoglobulin A (IgA) nephropathy, 2 with membranous nephropathy, 1 with anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis, and 1 with secondary focal segmental glomerulosclerosis (FSGS). All patients with IgA nephropathy had latent IgA deposition on their baseline biopsy. One patient with membranous nephropathy demonstrated findings of membranous nephropathy on the baseline biopsy, despite being asymptomatic. All patients, except for those with ANCA-associated nephropathy and secondary FSGS, recovered from the nephritis or maintained an adequate renal function after treatment.
Discussion/Conclusion:
Baseline biopsy is necessary for assessing the renal condition of kidney donors, and these donors require long-term follow-up based on their baseline biopsy findings. If donors develop kidney disease, appropriate diagnosis and treatment are essential.
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