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.

Abstract

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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