Literature DB >> 16879107

Treatment aspects of primary nephrotic syndrome in adults.

Senija Rasić1, Snjezana Uncanin, Jasminka Dzemidzić, Kenana Aganović, Amira Srna, Ismar Rasić.   

Abstract

Strict therapy protocol, which would be used universally for certain morphological forms of primary nephrotic syndrome, does not exist. The aim of the study was to show the effects of used therapy protocol in treatment of primary nephrotic syndrome at the Institute of Nephrology, Clinical Center University of Sarajevo in period of 2000-2005. The retrospective analysis covered 48 patients (17 women and 31 men) with idiopathic nephrotic syndrome, where pathomorphological changes were proved by kidney biopsy. Minimal change disease was confirmed with 6 (12.5%) patients. All patients were initially treated with corticosteroids with dose of 1 mg/kg of body weight. Five patients were in the group of primary responders (83.3%) with long term total remission, and 1 patient (16.6%) was a primary responder with 3 relapses in 8 months with a therapy of corticosteroids and bolus of cyclophosphamide. Diffuse mesangial proliferative glomerulonephritis was shown in 13 patients (27.1%). Seven patients from this group were treated with corticosteroid therapy (1 mg/kg of body weight for 4 weeks, followed by 0.5 mg/ kg of body weight until therapeutical response was achieved, and finally gradual exclusion of therapy after eight weeks in responsive patients). Six patients were treated with corticosteroids and one-month of bolus cyclophosphamide during half of year (10-5 mg/kg of body weight). Total remission was achieved in 37,9% of the patients. The IgA nephropathy presented with the nephrotic syndrome was shown in 10.4% (5) of the patients. Three patients from this group were treated with corticosteroid therapy (1 mg/kg of body weight for 4 weeks, followed by 0,5 mg/ kg of body weight until therapeutical response was achieved, and finally gradual exclusion of therapy after eight weeks in responsive patients) and.2 patients with corticosteroids and cyclophosphamide (1.5 mg/kg of body weight) during 6 months. Complete remission of nephrotic syndrome from this pathomorphological category was achieved in 2 patients. Membranoproliferative glomerulonephritis was shown in 6 patients (12.5%). All were treated with corticosteroids plus bolus of cyclophosphamide. Partial remission was achieved in one patient. Membranous glomerulonephritis was confirmed in 18 patients (37.5 %). Combined therapy of corticosteroids and bolus of cyclophosphamide was used in 7/18 patients, in 2/18 patients therapy of corticosteroids and per os cyclophosphamide (2 mg/kg of body weight) and in 9/18 patients cyclosporine therapy (3 mg/kg of body weight). Complete remission was achieved in 38.8% of the patients. A high percentage of achieved remissions of primary nephrotic syndrome in adults shows the efficiency of immunomodulating therapy used. Membranoproliferative glomerulonephritis still remains a therapy problem.

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Year:  2006        PMID: 16879107      PMCID: PMC7192645          DOI: 10.17305/bjbms.2006.3166

Source DB:  PubMed          Journal:  Bosn J Basic Med Sci        ISSN: 1512-8601            Impact factor:   3.363


  11 in total

Review 1.  Treatment of the idiopathic nephrotic syndrome: regimens and outcomes in children and adults.

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Journal:  J Am Soc Nephrol       Date:  1997-05       Impact factor: 10.121

2.  Cyclosporine in patients with steroid-resistant membranous nephropathy: a randomized trial.

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Review 3.  What is new in therapy of glomerulonephritis in 2003/2004.

Authors:  Z Hruby
Journal:  Rocz Akad Med Bialymst       Date:  2004

4.  Adult-onset idiopathic nephrotic syndrome associated with pure diffuse mesangial hypercellularity.

Authors:  E Alexopoulos; A Papagianni; M Stangou; A Pantzaki; M Papadimitriou
Journal:  Nephrol Dial Transplant       Date:  2000-07       Impact factor: 5.992

5.  Adult-onset minimal change nephrotic syndrome: a long-term follow-up.

Authors:  F Nolasco; J S Cameron; E F Heywood; J Hicks; C Ogg; D G Williams
Journal:  Kidney Int       Date:  1986-06       Impact factor: 10.612

6.  Controlled, prospective trial of steroid treatment in IgA nephropathy: a limitation of low-dose prednisolone therapy.

Authors:  Ritsuko Katafuchi; Kiyoshi Ikeda; Tohru Mizumasa; Hiroshi Tanaka; Takashi Ando; Tetsuro Yanase; Kohsuke Masutani; Michiaki Kubo; Satoru Fujimi
Journal:  Am J Kidney Dis       Date:  2003-05       Impact factor: 8.860

Review 7.  New perspectives in treatment of glomerulonephritis.

Authors:  Rosanna Coppo; Alessandro Amore
Journal:  Pediatr Nephrol       Date:  2003-12-13       Impact factor: 3.714

Review 8.  IgA nephropathy.

Authors:  J H Galla
Journal:  Kidney Int       Date:  1995-02       Impact factor: 10.612

9.  Glucocorticoid receptors, in vitro steroid sensitivity, and cytokine secretion in idiopathic nephrotic syndrome.

Authors:  Ana Paula de Carvalho Panzeri Carlotti; Paulo Benedito Franco; Lucila Leico Elias; Inalda Facincani; Elaine Lourenço Cardeal Costa; Norma Foss; Ayrton Custódio Moreira; Margaret de Castro
Journal:  Kidney Int       Date:  2004-02       Impact factor: 10.612

10.  A review of therapeutic studies of idiopathic membranous glomerulopathy.

Authors:  S L Hogan; K E Muller; J C Jennette; R J Falk
Journal:  Am J Kidney Dis       Date:  1995-06       Impact factor: 8.860

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