Literature DB >> 21493743

Long-term results of a randomized controlled trial in childhood IgA nephropathy.

Koichi Kamei1, Koichi Nakanishi, Shuichi Ito, Mari Saito, Mayumi Sako, Kenji Ishikura, Hiroshi Hataya, Masataka Honda, Kazumoto Iijima, Norishige Yoshikawa.   

Abstract

BACKGROUND AND OBJECTIVES: Children with IgA nephropathy showing diffuse (>80%) mesangial proliferation are at high risk for end-stage renal failure (ESRF). A previous controlled trial showed that combination therapy consisting of prednisolone, azathioprine, heparin-warfarin, and dipyridamole early in the course of disease reduces immunologic renal injury and prevents the progression of sclerosed glomeruli. The objective of this study was to evaluate the long-term effectiveness of combination therapy in children with IgA nephropathy showing diffuse mesangial proliferation. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: A secondary analysis of a multicenter, randomized, controlled trial involving 78 children with IgA nephropathy who received either 2-year combination therapy or heparin-warfarin and dipyridamole (control) therapy was conducted.
RESULTS: The median duration of observation was 10 years (range, 0.5 to 18). Two of 40 patients (5%) who received combination therapy and five of 34 patients (14.7%) who received control therapy developed ESRF. A Kaplan-Meier plot of renal survival showed that the outcomes of patients in the combined therapy group were better than those in the control therapy group (log-rank P = 0.03). The 10-year renal survival probability of each group was 97.1% (95% confidence interval, 81.4 to 99.6%) and 84.8% (95% confidence interval, 55.4 to 95.5%), respectively. The Cox proportional hazards model showed that the 2-year combination therapy was significantly associated with renal survival in both univariate and multivariate analyses.
CONCLUSIONS: Two-year combination therapy not only ameliorated the activity of the acute phase of nephritis but also improved the long-term outcome of severe childhood IgA nephropathy.

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Year:  2011        PMID: 21493743      PMCID: PMC3109925          DOI: 10.2215/CJN.08630910

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  29 in total

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Authors:  Rosanna Coppo; Giuseppe D'Amico
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Review 2.  Treatment of IgA nephropathy.

Authors:  J Barratt; J Feehally
Journal:  Kidney Int       Date:  2006-06       Impact factor: 10.612

Review 3.  The IgA nephropathy treatment dilemma.

Authors:  G B Appel; M Waldman
Journal:  Kidney Int       Date:  2006-06       Impact factor: 10.612

4.  Corticosteroids in IgA nephropathy: a randomised controlled trial.

Authors:  C Pozzi; P G Bolasco; G B Fogazzi; S Andrulli; P Altieri; C Ponticelli; F Locatelli
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5.  Alternate-day prednisone therapy in IgA nephropathy. Preliminary analysis of a prospective, randomized, controlled trial.

Authors:  B A Julian; C Barker
Journal:  Contrib Nephrol       Date:  1993       Impact factor: 1.580

6.  Can immunosuppressive drugs slow the progression of IgA nephropathy?

Authors:  D Goumenos; M Ahuja; J R Shortland; C B Brown
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8.  Combination therapy with mizoribine for severe childhood IgA nephropathy: a pilot study.

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9.  Steroid treatment for severe childhood IgA nephropathy: a randomized, controlled trial.

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Journal:  Clin J Am Soc Nephrol       Date:  2006-04-05       Impact factor: 8.237

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3.  Validity of the Oxford classification of IgA nephropathy in children.

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5.  Combination therapy with or without warfarin and dipyridamole for severe childhood IgA nephropathy: an RCT.

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6.  Long-term morbidity of IgA nephropathy in children evaluated with newly proposed remission criteria in Japan.

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8.  Risk factors for persistent proteinuria after a 2-year combination therapy for severe childhood IgA nephropathy.

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9.  Comparison of long-term follow-up outcomes between multiple-drugs combination therapy and tonsillectomy pulse therapy for pediatric IgA nephropathy.

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10.  Successful therapy with tonsillectomy plus pulse therapy for the relapse of pediatric IgA nephropathy treated with multi-drugs combination therapy.

Authors:  Nobuko Sakai; Yukihiko Kawasaki; Tomoko Waragai; Tomoko Oikawa; Masatoshi Kaneko; Tomoko Sato; Kazuhide Suyama; Mitsuaki Hosoya
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