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Repeated Kidney Biopsy in Membranoproliferative Glomerulonephritis
Ai-Hui Li1,2,3,4,5, Yang Li1,2,3,4,5, Meng-Shi Li1,2,3,4,5
1Renal Division, Peking University First Hospital, Beijing, China.
Introduction:
Membranoproliferative glomerulonephritis (MPGN) is a heterogeneous pattern of glomerular injury. Repeated kidney biopsies may elucidate pathogenic mechanisms and guide diagnostic strategies.
Methods:
We included 82 patients diagnosed with MPGN by kidney biopsy who underwent at least two biopsies between 1997 and 2023 at Peking University First Hospital. Clinical and pathological data were analyzed retrospectively.
Results:
Of 342 MPGN patients, 95 (28%) had repeated biopsies (0.9-4.0 years apart). This incidence was higher than in other glomerulonephropathies under immunosuppression. Among the 82 patients analyzed (excluding kidney transplants and ≤3-month biopsy intervals), 42 were initially diagnosed with non-MPGN pathology. At the second biopsy, proteinuria increased (from 2.9 to 6.3 g/day), eGFR declined (from 76 to 47 mL/min/1.73 m2), and renal C3 deposition was stronger (p = 0.04). Thirty patients (37%) had etiological reclassification, mostly to monoclonal gammopathy of renal significance (MGRS). Compared to idiopathic MPGN, MGRS patients were older (53 vs. 35 years) and had worse renal function (eGFR 57 vs. 81 mL/min/1.73 m2) but slower eGFR decline (-7 vs. -12 mL/min/1.73 m2/year). Most MGRS patients (64%) remained negative for monoclonal protein in serum or urine immunofixation, necessitating repeat biopsy and clone-directed therapy.
Conclusion:
In this study, about half and one-third of patients underwent morphological and etiological reclassification, respectively. Stronger complement deposition may drive morphological changes. Repeated kidney biopsies are crucial for diagnosing MGRS, especially in patients with negative immunofixation.
Insights
Repeated kidney biopsies are vital for diagnosing membranoproliferative glomerulonephritis (MPGN), especially for identifying monoclonal gammopathy of renal significance (MGRS) when initial tests are negative.
Area of Science:
- Nephrology
- Pathology
- Immunology
Background:
- Membranoproliferative glomerulonephritis (MPGN) is a complex glomerular disease with heterogeneous presentations.
- Accurate diagnosis and pathogenic understanding of MPGN often require serial investigations.
Purpose of the Study:
- To evaluate the diagnostic yield of repeated kidney biopsies in patients with MPGN.
- To assess changes in clinical and pathological findings and reclassification rates, particularly for monoclonal gammopathy of renal significance (MGRS).
Main Methods:
- Retrospective analysis of clinical and pathological data from 82 patients with MPGN who underwent at least two kidney biopsies.
- Comparison of findings between initial and subsequent biopsies, including proteinuria, estimated glomerular filtration rate (eGFR), and renal complement deposition.
- Analysis of etiological reclassification, focusing on the distinction between idiopathic MPGN and MGRS.
Main Results:
- Approximately 28% of MPGN patients underwent repeat biopsies, a higher incidence than in other glomerulonephropathies under immunosuppression.
- Repeat biopsies revealed significant increases in proteinuria and renal C3 deposition, along with a decline in eGFR.
- Thirty-seven percent of patients were reclassified etiologically, predominantly to MGRS, which was associated with older age and poorer renal function but slower eGFR decline compared to idiopathic MPGN.
- A significant proportion of MGRS patients (64%) tested negative for monoclonal proteins in initial serum or urine immunofixation.
Conclusions:
- Repeated kidney biopsies are essential for morphological and etiological reclassification in MPGN, with about half and one-third of patients benefiting, respectively.
- Stronger complement deposition may correlate with morphological changes observed in serial biopsies.
- Repeat kidney biopsies are critical for diagnosing MGRS, particularly in cases with initially negative immunofixation results, guiding targeted therapy.
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