Literature DB >> 16785738

Immunosuppressive treatment of idiopathic focal segmental glomerulosclerosis: a five-year follow-up study.

Dimitrios S Goumenos1, George Tsagalis, A Meguid El Nahas, John R Shortland, Periklis Davlouros, John G Vlachojannis, Colin B Brown.   

Abstract

BACKGROUND/AIMS: Focal segmental glomerulosclerosis (FSGS) is a common type of glomerular disease that can lead to chronic renal failure. Various therapeutic regimens have been used in nephrotic FSGS patients. The effect of treatment with prednisolone alone or its combination with azathioprine and cyclosporin and parameters related to a poor outcome are studied.
METHODS: Fifty-one patients with idiopathic FSGS and a follow-up period of 5 years were included. Twenty-five were treated with prednisolone alone (1 mg/kg BW/day) or combination of prednisolone (0.5 mg/kg BW/day) with azathioprine (2 mg/kg BW/day) or cyclosporine (3 mg/kg BW/day) in gradually reduced doses whereas 26 patients received no immunosuppressive drugs. Lower prednisolone dose regimens were used as initial treatment in obese, borderline diabetics or patients with bone disease. The clinical course was estimated using the end-points of 50% or doubling of baseline serum creatinine and/or end-stage renal failure. The contribution of clinical and histological parameters in the clinical outcome was estimated by univariate and multivariate analyses.
RESULTS: Increase of baseline serum creatinine by 50% during the follow-up period was observed in 2 treated and 9 untreated patients (8% vs. 35%, p = 0.03) whereas doubling of serum creatinine in 2 and 5 patients respectively (8% vs. 19%, p = NS). End-stage renal failure developed in 4 of 51 patients (8%), 2 treated and 2 untreated (p = NS). Parameters related to a poor outcome were baseline serum creatinine and severity of glomerulosclerosis (multivariate analysis OR = 1.08, p = 0.01). Most of patients (68%) who reached end-points had persistent nephrotic syndrome during the follow-up. Remission of nephrotic syndrome was observed more frequently among treated (75 vs. 30.7%, p = 0.05). Prednisolone alone was followed by remission of nephrotic syndrome in 62.5% whereas combination of lower prednisolone dose with azathioprine and cyclosporin in 80 and 85.7% of patients. No serious side-effects were observed.
CONCLUSION: This and previous studies suggest that steroid and/or immunosuppressive therapy have a role in amelioration of the clinical course and remission of nephrotic syndrome in patients with FSGS A combination of low predisolone dose with cyclosporine could be used as initial treatment in patients with higher risk for side-effects from the usual prednisolone dose. Copyright 2006 S. Karger AG, Basel.

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Year:  2006        PMID: 16785738     DOI: 10.1159/000093993

Source DB:  PubMed          Journal:  Nephron Clin Pract        ISSN: 1660-2110


  16 in total

1.  A novel multidrug therapy for difficult cyclosporine-resistant focal segmental glomerulosclerosis.

Authors:  Eishin Oki; Kazushi Tsuruga; Masanobu Kudo; Koji Tsugawa; Koichi Suzuki; Hiroshi Tanaka
Journal:  Pediatr Nephrol       Date:  2008-10-24       Impact factor: 3.714

2.  Collapsing focal segmental glomerulosclerosis: Current concepts.

Authors:  Muhammed Mubarak
Journal:  World J Nephrol       Date:  2012-04-06

3.  Rethinking First-Line Immunosuppression for Idiopathic FSGS.

Authors:  Jordana B Cohen; Jonathan J Hogan
Journal:  Clin J Am Soc Nephrol       Date:  2016-02-16       Impact factor: 8.237

4.  Prospective 5-year follow-up of cyclosporine treatment in children with steroid-resistant nephrosis.

Authors:  Yuko Hamasaki; Norishige Yoshikawa; Hitoshi Nakazato; Satoshi Sasaki; Kazumoto Iijima; Koichi Nakanishi; Takeshi Matsuyama; Kenji Ishikura; Shuichi Ito; Tetsuji Kaneko; Masataka Honda
Journal:  Pediatr Nephrol       Date:  2013-01-13       Impact factor: 3.714

5.  Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS.

Authors:  Lawrence Copelovitch; Marta Guttenberg; Martin R Pollak; Bernard S Kaplan
Journal:  Pediatr Nephrol       Date:  2007-05-25       Impact factor: 3.714

6.  Corticosteroids vs. corticosteroids plus cycloporin A in adult minimal changes disease.

Authors:  Dimitrios S Goumenos; Pantelitsa Kalliakmani; Eirini Savvidaki; John G Vlachojannis
Journal:  BMC Res Notes       Date:  2009-07-22

Review 7.  Immunosuppressive treatment for focal segmental glomerulosclerosis in adults.

Authors:  Norbert Braun; Frank Schmutzler; Catalina Lange; Annalisa Perna; Giuseppe Remuzzi; Teut Risler; Narelle S Willis
Journal:  Cochrane Database Syst Rev       Date:  2008-07-16

8.  Citral is renoprotective for focal segmental glomerulosclerosis by inhibiting oxidative stress and apoptosis and activating Nrf2 pathway in mice.

Authors:  Shun-Min Yang; Kuo-Feng Hua; Yu-Chuan Lin; Ann Chen; Jia-Ming Chang; Louis Kuoping Chao; Chen-Lung Ho; Shuk-Man Ka
Journal:  PLoS One       Date:  2013-09-17       Impact factor: 3.240

9.  Chapter 6: Idiopathic focal segmental glomerulosclerosis in adults.

Authors: 
Journal:  Kidney Int Suppl (2011)       Date:  2012-06

Review 10.  Treatment Strategies of Adult Primary Focal Segmental Glomerulosclerosis: A Systematic Review Focusing on the Last Two Decades.

Authors:  Arno Beer; Gert Mayer; Andreas Kronbichler
Journal:  Biomed Res Int       Date:  2016-04-07       Impact factor: 3.411

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