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免疫球蛋白 A 肾病的皮质类固醇治疗:是敌是友?

Corticosteroid Therapy in Immunoglobulin A Nephropathy: A Friend or Foe?

机构信息

Renal and Metabolic Division, The George Institute for Global Health, Newtown, New South Wales, Australia.

Concord Clinical School, University of Sydney, Concord, New South Wales, Australia.

出版信息

Kidney Blood Press Res. 2023;48(1):392-404. doi: 10.1159/000530285. Epub 2023 Mar 27.

Abstract

BACKGROUND

The administration of corticosteroids in addition to supportive care to delay progressive immunoglobulin A nephropathy (IgAN), the most common primary glomerulonephritis worldwide, remains controversial. This is partly due to the paucity of well-designed randomized controlled trials and well-known corticosteroid-related side effects. As a result, clinical equipoise in corticosteroid therapy exists depending on geographical regions and the clinician's preference.

SUMMARY

Better understanding around the pathogenesis of IgAN has prompted several clinical trials exploring the effects of immunosuppressive agents including corticosteroids. Earlier studies of corticosteroids were limited by suboptimal study designs, inadequate implementation of standard of care, and inconsistent adverse event data collection. Two well-designed, adequately powered, multi-centre randomized controlled trials, the STOP-IgAN and TESTING studies, have reported contrasting kidney outcomes that have further fuelled the clinical conundrum regarding the efficacy of corticosteroids. Both studies independently reported greater adverse events with corticosteroids. A novel targeted release formulation of budesonide, which has been hypothesized to reduce the adverse events associated with systemic corticosteroids, has shown promising results in the Phase 3 NefigaRD trial. Studies of treatments targeting B cells and the complement cascade are currently underway, and early data appear encouraging. This review provides an overview of the current literature around the understanding of the pathomechanisms and benefits and harm of corticosteroid use in IgAN.

KEY MESSAGES

Recent evidence suggests the use of corticosteroids in a selected cohort of people with IgAN at high risk of disease progression can improve kidney outcomes but comes with an associated risk of treatment-related adverse events, particularly with higher doses. Management decisions should therefore follow an informed patient-clinician discussion.

摘要

背景

在支持性治疗之外,联合应用皮质类固醇治疗免疫球蛋白 A 肾病(IgAN)——目前全球最常见的原发性肾小球肾炎——仍存在争议。这在一定程度上是由于缺乏精心设计的随机对照试验以及皮质类固醇相关的已知副作用。因此,皮质类固醇治疗的临床平衡取决于地理位置和临床医生的偏好。

总结

对 IgAN 发病机制的更好理解促使人们开展了几项探索免疫抑制剂(包括皮质类固醇)作用的临床试验。早期的皮质类固醇研究受到不理想的研究设计、标准治疗实施不足以及不良事件数据收集不一致的限制。两项精心设计、充分有力、多中心的随机对照试验,即 STOP-IgAN 和 TESTING 研究,报告了相互矛盾的肾脏结局,这进一步加剧了皮质类固醇疗效的临床难题。这两项研究均独立报告了皮质类固醇治疗的不良事件更多。布地奈德的一种新型靶向释放制剂,该制剂被假设可以减少与全身皮质类固醇相关的不良反应,在 3 期 NefigaRD 试验中显示出了有希望的结果。目前正在进行针对 B 细胞和补体级联的治疗研究,早期数据令人鼓舞。这篇综述提供了 IgAN 中皮质类固醇作用的发病机制、获益和危害的当前文献概述。

关键信息

最近的证据表明,在 IgAN 中具有高疾病进展风险的特定人群中使用皮质类固醇可以改善肾脏结局,但会带来与治疗相关的不良反应风险,特别是在使用更高剂量时。因此,管理决策应遵循知情的医患讨论。

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