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Clinical features of thin basement membrane disease and associated glomerulopathies
Yuh-Mou Sue1, Jeng-Jong Huang, Ryh-Yaw Hsieh
1Department of Internal Medicine, Taipei Medical University Municipal Wan Fang Hospital, Taipei, Taiwan.
Background:
Thin basement membrane disease (TBMD) occurs in 5-11% of renal biopsy series, and can be associated with other glomerulopathies (GNs). Data on the prevalence, clinical features, and prognosis of TBMD with other GNs are limited.
Methods And Results:
From June 1990 to May 2001, findings from 658 native kidney biopsies were retrospectively studied. The overall prevalence of TBMD was 7.9% (52 of 658). The mean glomerular basement membrane (GBM) thickness was 206 +/- 30 nm. Clinicopathological features were compared for patients with TBMD only (n = 14) and in those with TBMD and GN (n = 38). Focal segmental glomerulosclerosis, mesangial proliferative GN, and minimal change disease were the most common GNs associated with TBMD. After a mean follow-up period of 44.9 +/- 42.5 months, the group who only had TBMD revealed a relatively benign disease with microscopic haematuria and trivial proteinuria, a low prevalence of hypertension, and no renal progression. In the group who had both TBMD and GN, heavy proteinuria (6.1 +/- 5.2 g/day), hypoalbuminaemia (26 +/- 12 g/L) and renal insufficiency (76 +/- 25 mL/min) might develop.
Conclusion:
We suggested that the TBMD is a developmental abnormality of little or no significance and that it is the underlying associated GN rather than TBMD, which has the relevance to the outcome of renal disease.
Insights
Thin basement membrane disease (TBMD) is often benign. Associated glomerulopathies (GNs), not TBMD itself, determine the renal disease outcome and prognosis.
Area of Science:
- Nephrology
- Pathology
- Glomerular Diseases
Background:
- Thin basement membrane disease (TBMD) is found in 5-11% of renal biopsies.
- Its association with other glomerulopathies (GNs) and subsequent prognosis are not well-documented.
Purpose of the Study:
- To determine the prevalence, clinical features, and prognosis of TBMD.
- To investigate the impact of co-existing GNs on TBMD outcomes.
Main Methods:
- Retrospective analysis of 658 native kidney biopsies from June 1990 to May 2001.
- Comparison of clinicopathological features between TBMD-only and TBMD with GN groups.
- Mean follow-up of 44.9 months.
Main Results:
- TBMD prevalence was 7.9% (52/658) with a mean GBM thickness of 206 nm.
- TBMD-only group showed benign findings: microscopic hematuria, minimal proteinuria, low hypertension, and no progression.
- TBMD with GN group presented with heavy proteinuria, hypoalbuminemia, and renal insufficiency.
Conclusions:
- TBMD is likely a developmental abnormality with minimal clinical significance.
- The prognosis of renal disease in patients with TBMD is primarily determined by the co-existing glomerulopathy.
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