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The improvement of renal survival with steroid pulse therapy in IgA nephropathy
Background. The benefits of steroid therapy in immunoglobulin A nephropathy (IgAN) have not been established. Methods. The effect of steroids on kidney survival was retrospectively investigated in 702 patients with IgAN by multivariate analyses. Results. There were 295 men and 407 women. The median...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639065/ https://www.ncbi.nlm.nih.gov/pubmed/18644797 http://dx.doi.org/10.1093/ndt/gfn394 |
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author | Katafuchi, Ritsuko Ninomiya, Toshiharu Mizumasa, Tohru Ikeda, Kiyoshi Kumagai, Harumitsu Nagata, Masaharu Hirakata, Hideki |
author_facet | Katafuchi, Ritsuko Ninomiya, Toshiharu Mizumasa, Tohru Ikeda, Kiyoshi Kumagai, Harumitsu Nagata, Masaharu Hirakata, Hideki |
author_sort | Katafuchi, Ritsuko |
collection | PubMed |
description | Background. The benefits of steroid therapy in immunoglobulin A nephropathy (IgAN) have not been established. Methods. The effect of steroids on kidney survival was retrospectively investigated in 702 patients with IgAN by multivariate analyses. Results. There were 295 men and 407 women. The median follow-up period was 62 months. One hundred and ninety-four patients were treated with oral steroids (oral steroid group). Thirty-four patients were treated with methylprednisolone (mPSL) pulse therapy (pulse steroid group) followed by oral prednisolone (PSL). In 474 patients, no steroid was used (no steroid group). The urinary protein-creatinine ratio and histological grade were significantly different among treatment groups and were highest in the pulse steroid group followed by the oral steroid group and lowest in the no steroid patients. Serum creatinine was significantly higher in the pulse steroid group than in other two groups. Eighty-five patients developed end-stage renal failure (ESRF) requiring haemodialysis. In multivariate analysis, steroid pulse therapy significantly decreased the risk of ESRF while oral steroid treatment did not improve renal survival in this cohort. Conclusion. We found that pulse steroid therapy improved kidney survivals in IgAN. Since the clinical findings and histological grade were the most severe in patients treated with mPSL pulse therapy, such therapy may prevent progression of IgAN. |
format | Text |
id | pubmed-2639065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26390652009-02-25 The improvement of renal survival with steroid pulse therapy in IgA nephropathy Katafuchi, Ritsuko Ninomiya, Toshiharu Mizumasa, Tohru Ikeda, Kiyoshi Kumagai, Harumitsu Nagata, Masaharu Hirakata, Hideki Nephrol Dial Transplant Clinical Nephrology Background. The benefits of steroid therapy in immunoglobulin A nephropathy (IgAN) have not been established. Methods. The effect of steroids on kidney survival was retrospectively investigated in 702 patients with IgAN by multivariate analyses. Results. There were 295 men and 407 women. The median follow-up period was 62 months. One hundred and ninety-four patients were treated with oral steroids (oral steroid group). Thirty-four patients were treated with methylprednisolone (mPSL) pulse therapy (pulse steroid group) followed by oral prednisolone (PSL). In 474 patients, no steroid was used (no steroid group). The urinary protein-creatinine ratio and histological grade were significantly different among treatment groups and were highest in the pulse steroid group followed by the oral steroid group and lowest in the no steroid patients. Serum creatinine was significantly higher in the pulse steroid group than in other two groups. Eighty-five patients developed end-stage renal failure (ESRF) requiring haemodialysis. In multivariate analysis, steroid pulse therapy significantly decreased the risk of ESRF while oral steroid treatment did not improve renal survival in this cohort. Conclusion. We found that pulse steroid therapy improved kidney survivals in IgAN. Since the clinical findings and histological grade were the most severe in patients treated with mPSL pulse therapy, such therapy may prevent progression of IgAN. Oxford University Press 2008-12 2008-07-20 /pmc/articles/PMC2639065/ /pubmed/18644797 http://dx.doi.org/10.1093/ndt/gfn394 Text en © The Author [2008]. http://creativecommons.org/licenses/by-nc/2.0/uk/ The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Clinical Nephrology Katafuchi, Ritsuko Ninomiya, Toshiharu Mizumasa, Tohru Ikeda, Kiyoshi Kumagai, Harumitsu Nagata, Masaharu Hirakata, Hideki The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title | The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title_full | The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title_fullStr | The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title_full_unstemmed | The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title_short | The improvement of renal survival with steroid pulse therapy in IgA nephropathy |
title_sort | improvement of renal survival with steroid pulse therapy in iga nephropathy |
topic | Clinical Nephrology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639065/ https://www.ncbi.nlm.nih.gov/pubmed/18644797 http://dx.doi.org/10.1093/ndt/gfn394 |
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