Literature DB >> 14996302

Clinical features of thin basement membrane disease and associated glomerulopathies.

Yuh-Mou Sue1, Jeng-Jong Huang, Ryh-Yaw Hsieh, Fen-Fen Chen.   

Abstract

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.

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Year:  2004        PMID: 14996302     DOI: 10.1111/j.1440-1797.2003.00223.x

Source DB:  PubMed          Journal:  Nephrology (Carlton)        ISSN: 1320-5358            Impact factor:   2.506


  5 in total

1.  Pattern of double glomerulopathy in children.

Authors:  Hae Il Cheong; Hee Yeon Cho; Kyung Chul Moon; Il Soo Ha; Yong Choi
Journal:  Pediatr Nephrol       Date:  2006-11-16       Impact factor: 3.714

2.  Pathologic glomerular characteristics and glomerular basement membrane alterations in biopsy-proven thin basement membrane nephropathy.

Authors:  Yusuke Kajimoto; Yoko Endo; Mika Terasaki; Shinobu Kunugi; Toru Igarashi; Akiko Mii; Yasuhiro Terasaki; Akira Shimizu
Journal:  Clin Exp Nephrol       Date:  2019-01-28       Impact factor: 2.801

3.  Co-existence of thin basement membrane nephropathy with other glomerular pathologies; a single center experience.

Authors:  Rizwan A Qazi; Bahar Bastani
Journal:  J Nephropathol       Date:  2015-04-01

4.  Clinical manifestations of IgA nephropathy combined with thin glomerular basement membrane nephropathy in children.

Authors:  Young Ju Hwang; Dong Sub Kim; Cheol Woo Ko; Min Hyun Cho; Tae In Park
Journal:  Kidney Res Clin Pract       Date:  2013-09-04

5.  Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.

Authors:  Andrew F Malone; Paul J Phelan; Gentzon Hall; Umran Cetincelik; Alison Homstad; Andrea S Alonso; Ruiji Jiang; Thomas B Lindsey; Guanghong Wu; Matthew A Sparks; Stephen R Smith; Nicholas J A Webb; Philip A Kalra; Adebowale A Adeyemo; Andrey S Shaw; Peter J Conlon; J Charles Jennette; David N Howell; Michelle P Winn; Rasheed A Gbadegesin
Journal:  Kidney Int       Date:  2014-09-17       Impact factor: 10.612

  5 in total

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