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Review
. 2017:2017:7689254.
doi: 10.1155/2017/7689254. Epub 2017 May 3.

Recent Treatment Advances and New Trials in Adult Nephrotic Syndrome

Affiliations
Review

Recent Treatment Advances and New Trials in Adult Nephrotic Syndrome

Eva Königshausen et al. Biomed Res Int. 2017.

Abstract

The etiology of nephrotic syndrome is complex and ranges from primary glomerulonephritis to secondary forms. Patients with nephrotic syndrome often need immunosuppressive treatment with its side effects and may progress to end stage renal disease. This review focuses on recent advances in the treatment of primary causes of nephrotic syndrome (idiopathic membranous nephropathy (iMN), minimal change disease (MCD), and focal segmental glomerulosclerosis (FSGS)) since the publication of the KDIGO guidelines in 2012. Current treatment recommendations are mostly based on randomized controlled trials (RCTs) in children, small RCTs, or case series in adults. Recently, only a few new RCTs have been published, such as the Gemritux trial evaluating rituximab treatment versus supportive antiproteinuric and antihypertensive therapy in iMN. Many RCTs are ongoing for iMN, MCD, and FSGS that will provide further information on the effectiveness of different treatment options for the causative disease. In addition to reviewing recent clinical studies, we provide insight into potential new targets for the treatment of nephrotic syndrome from recent basic science publications.

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References

    1. Kidney Disease: Improving Global Outcomes (KDIGO) Glomerulonephritis Work Group. KDIGO Clinical Practice Guideline for Glomerulonephritis. Kidney International. 2012;2(supplement 2):139–274.
    1. Floege J., Amann K. Primary glomerulonephritides. The Lancet. 2016;387(10032):2036–2048. doi: 10.1016/S0140-6736(16)00272-5. - DOI - PubMed
    1. Ruggenenti P., Perticucci E., Cravedi P., et al. Role of remission clinics in the longitudinal treatment of CKD. Journal of the American Society of Nephrology. 2008;19(6):1213–1224. doi: 10.1681/ASN.2007090970. - DOI - PMC - PubMed
    1. Barbour S. J., Greenwald A., Djurdjev O., et al. Disease-specific risk of venous thromboembolic events is increased in idiopathic glomerulonephritis. Kidney International. 2012;81(2):190–195. doi: 10.1038/ki.2011.312. - DOI - PubMed
    1. Lee T., Biddle A. K., Lionaki S., et al. Personalized prophylactic anticoagulation decision analysis in patients with membranous nephropathy. Kidney International. 2014;85(6):1412–1420. doi: 10.1038/ki.2013.476. - DOI - PMC - PubMed

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