Literature DB >> 26743078

Treatment of IgA nephropathy with renal insufficiency.

Claudio Pozzi1, Cristina Sarcina2, Francesca Ferrario2.   

Abstract

IgA Nephropathy leads young people to dialysis more often than other glomerular diseases, because often diagnosis and therapy are made late. Nephrologists waive to treat IgAN pts with chronic renal insufficiency, believing that treatment may not be effective and safe. Moreover, studies in IgAN pts with reduced renal function are lacking. Small studies seem to indicate a possible utility of RAS blockers and corticosteroids in these patients. Recently, VALIGA study showed that corticosteroids and immunosuppressants were more frequently used in pts with eGFR <30 ml/min than in those with eGFR >30 ml/min (60 vs. 44 %, respectively; p = 0.004). The goal of treating IgAN pts is to obtain a time-average proteinuria <1 g/day, regardless of the degree of renal function and histological damage. RASB and corticosteroids seem to be able to obtain this result. However, it's important to pay attention to the appearance of adverse events of CS. In the literature, major side effects occurred in 29 of 463 (6.2 %) patients enrolled in RCTs. However, scarce informations are obtained about the safety of CS in patients with reduced renal function. To better evaluate this aspect, we considered three studies, that used similar schemes of therapy and included patients with different degrees of renal function (1: GFR 90 ml/min/1.73 m(2), 2: 81 ml/min/1.73 m(2), 3: 34 ml/min/1.73 m(2)). The occurrence of adverse events increased with the worsening of renal function (2.3, 5.7 and 15.4 % in studies 1, 2 and 3 respectively). The aim of the treatment for a patient with an eGFR <30 is to slow the progression and to delay the need for dialysis. Therefore, in stage CKD 2, 3 and 4 with a proteinuria >1 g/day a 6-month course of corticosteroids could be useful and safe.

Entities:  

Keywords:  Chronic kidney disease; Corticosteroids; IgA nephropathy; Immunosuppressants; RAS blockers; Time-average proteinuria

Mesh:

Substances:

Year:  2016        PMID: 26743078     DOI: 10.1007/s40620-015-0257-2

Source DB:  PubMed          Journal:  J Nephrol        ISSN: 1121-8428            Impact factor:   3.902


  41 in total

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2.  Randomised placebo-controlled trial of effect of ramipril on decline in glomerular filtration rate and risk of terminal renal failure in proteinuric, non-diabetic nephropathy. The GISEN Group (Gruppo Italiano di Studi Epidemiologici in Nefrologia)

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Journal:  Lancet       Date:  1997-06-28       Impact factor: 79.321

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Journal:  Am J Kidney Dis       Date:  1991-07       Impact factor: 8.860

4.  In chronic nephropathies prolonged ACE inhibition can induce remission: dynamics of time-dependent changes in GFR. Investigators of the GISEN Group. Gruppo Italiano Studi Epidemiologici in Nefrologia.

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Journal:  J Am Soc Nephrol       Date:  1999-05       Impact factor: 10.121

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Authors:  Takahito Moriyama; Kazuho Honda; Kosaku Nitta; Wako Yumura; Hiroshi Nihei
Journal:  Clin Exp Nephrol       Date:  2004-09       Impact factor: 2.801

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Authors:  Heather N Reich; Stéphan Troyanov; James W Scholey; Daniel C Cattran
Journal:  J Am Soc Nephrol       Date:  2007-10-31       Impact factor: 10.121

7.  Treatment of IgA nephropathy with ACE inhibitors: a randomized and controlled trial.

Authors:  Manuel Praga; Eduardo Gutiérrez; Ester González; Enrique Morales; Eduardo Hernández
Journal:  J Am Soc Nephrol       Date:  2003-06       Impact factor: 10.121

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Authors:  Rosanna Coppo; Licia Peruzzi; Alessandro Amore; Antonio Piccoli; Pierre Cochat; Rosario Stone; Martin Kirschstein; Tommy Linné
Journal:  J Am Soc Nephrol       Date:  2007-05-18       Impact factor: 10.121

9.  A comparison of corticosteroid and warfarin therapy in IgA nephropathy with crescent formation: preliminary trial.

Authors:  Yoshihiko Kanno; Martje Witt; Hirokazu Okada; Hironori Nemoto; Soichi Sugahara; Hidetomo Nakamoto; Hiromichi Suzuki
Journal:  Clin Exp Nephrol       Date:  2003-03       Impact factor: 2.801

Review 10.  Effect of inhibitors of the renin-angiotensin system and other antihypertensive drugs on renal outcomes: systematic review and meta-analysis.

Authors:  Juan P Casas; Weiliang Chua; Stavros Loukogeorgakis; Patrick Vallance; Liam Smeeth; Aroon D Hingorani; Raymond J MacAllister
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  4 in total

1.  Treatment for IgA nephropathy with stage 3 or 4 chronic kidney disease: low-dose corticosteroids combined with oral cyclophosphamide.

Authors:  Feng Ma; Xiaoxia Yang; Meilan Zhou; Ming Bai; Lijuan Zhao; Li Li; Ruijuan Dong; Chunmei Liu; Rong Li; Shiren Sun
Journal:  J Nephrol       Date:  2020-05-23       Impact factor: 3.902

2.  Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.

Authors:  Annamaria Milillo; Clelia Molinario; Stefano Costanzi; Gisella Vischini; Francesca La Carpia; Francesco La Greca; Donato Rigante; Giovanni Gambaro; Fiorella Gurrieri; Eugenio Sangiorgi
Journal:  J Nephrol       Date:  2018-03-01       Impact factor: 3.902

3.  Effect of corticosteroids combined with cyclophosphamide or mycophenolate mofetil therapy for IgA nephropathy with stage 3 or 4 chronic kidney disease: A retrospective cohort study.

Authors:  Qing Jia; Feng Ma; Jin Zhao; Xiaoxia Yang; Ruiling Sun; Rong Li; Shiren Sun
Journal:  Front Pharmacol       Date:  2022-08-31       Impact factor: 5.988

4.  The effectiveness and safety of corticosteroid therapy for IgA nephropathy with crescents: a prospective, randomized, controlled study.

Authors:  Mengjun Liang; Liping Xiong; Aihua Li; Jiafan Zhou; Yajuan Huang; Miaofang Huang; Xing Zhang; Hongrui Shi; Ning Su; Yi Wei; Zongpei Jiang
Journal:  BMC Nephrol       Date:  2022-01-21       Impact factor: 2.388

  4 in total

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