Department of Nephrology, University Hospital, Medical Faculty, Heinrich-Heine University, Moorenstrasse 5, 40225 Duesseldorf, Germany.
Biomed Res Int. 2017;2017:7689254. doi: 10.1155/2017/7689254. Epub 2017 May 3.
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.
肾病综合征的病因复杂,范围从原发性肾小球肾炎到继发性疾病。肾病综合征患者通常需要免疫抑制治疗,但其有副作用,并可能进展为终末期肾病。本综述重点介绍了自 2012 年 KDIGO 指南发布以来,原发性肾病综合征(特发性膜性肾病(iMN)、微小病变性肾病(MCD)和局灶节段性肾小球硬化症(FSGS))治疗方面的最新进展。目前的治疗建议主要基于儿童的随机对照试验(RCT)、小型 RCT 或成人的病例系列研究。最近,只有少数新的 RCT 发表,例如 Gemritux 试验,评估利妥昔单抗治疗与 iMN 的支持性降蛋白尿和降压治疗相比。许多 RCT 正在进行中,用于 iMN、MCD 和 FSGS,将为病因疾病的不同治疗选择的有效性提供进一步的信息。除了回顾最近的临床研究外,我们还从最近的基础科学出版物中深入了解治疗肾病综合征的潜在新靶点。