Corticosteroids in IgA Nephropathy: Lessons from Recent Studies

被引:43
|
作者
Coppo, Rosanna [1 ]
机构
[1] Regina Margherita Hosp, Fdn Ric Molinette, Nephrol Dialysis & Transplantat, Piazza Polonia 94, I-10134 Turin, Italy
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2017年 / 28卷 / 01期
关键词
CARE PLUS IMMUNOSUPPRESSION; OXFORD CLASSIFICATION; PREDICTING PROGRESSION; ACE-INHIBITORS; PROTEINURIA; VALIDATION; THERAPY; TRIAL; REMISSION; PATHOPHYSIOLOGY;
D O I
10.1681/ASN.2016060647
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
IgA nephropathy (IgAN) is a common chronic glomerular disease that, in most patients, slowly progresses to ESRD. The immune and autoimmune responses that characterize IgAN indicate a potential benefit for corticosteroids. The 2012 Kidney Disease Improving Global Outcome (KDIGO) guidelines suggest giving corticosteroids to patients with rather preserved renal function (GFR>50 ml/min per 1.73 m(2)) and persistent proteinuria >1 g/d, despite 3-6 months of optimized supportive care with renin-angiotensin system blockers. However, the evidence supporting this guideline was considered of low quality. More recent results from large cohort studies and randomized, controlled trials have provided conflicting messages about the benefits of corticosteroid treatment over supportive care alone, mostly involving optimized renin-angiotensin system blockade, which might generate further uncertainty in the therapeutic choice. Overall, these results indicate that corticosteroids are a powerful tool for treating patients with IgAN; however, treatment success is not universal and mostly occurs in patients who are highly proteinuric with early CKD. In patients with advanced CKD, the side effects of corticosteroids increase, and the renal protection decreases. This brief review aimed at integrating the findings of these recently published reports to provide balanced advice for clinicians as well as suggestions for future trials.
引用
收藏
页码:25 / 33
页数:9
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