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基于尿肽的慢性肾脏病分类器CKD273:迈向慢性肾脏病的临床应用

Urinary peptide-based classifier CKD273: towards clinical application in chronic kidney disease.

作者信息

Pontillo Claudia, Mischak Harald

机构信息

Mosaiques Diagnostics, Hannover, Germany.

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.

出版信息

Clin Kidney J. 2017 Apr;10(2):192-201. doi: 10.1093/ckj/sfx002. Epub 2017 Mar 29.

Abstract

Capillary electrophoresis coupled with mass spectrometry (CE-MS) has been used as a platform for discovery and validation of urinary peptides associated with chronic kidney disease (CKD). CKD affects ∼ 10% of the population, with high associated costs for treatments. A urinary proteome-based classifier (CKD273) has been discovered and validated in cross-sectional and longitudinal studies to assess and predict the progression of CKD. It has been implemented in studies employing cohorts of > 1000 patients. CKD273 is commercially available as an diagnostic test for early detection of CKD and is currently being used for patient stratification in a multicentre randomized clinical trial (PRIORITY). The validity of the CKD273 classifier has recently been evaluated applying the Oxford Evidence-Based Medicine and Southampton Oxford Retrieval Team guidelines and a letter of support for CKD273 was issued by the US Food and Drug Administration. In this article we review the current evidence published on CKD273 and the challenges associated with implementation. Definition of a possible surrogate early endpoint combined with CKD273 as a biomarker for patient stratification currently appears as the most promising strategy to enable the development of effective drugs to be used at an early time point when intervention can still be effective.

摘要

毛细管电泳-质谱联用(CE-MS)已被用作发现和验证与慢性肾脏病(CKD)相关的尿肽的平台。CKD影响约10%的人口,治疗成本高昂。一种基于尿蛋白质组的分类器(CKD273)已在横断面和纵向研究中被发现并验证,用于评估和预测CKD的进展。它已在超过1000名患者的队列研究中得到应用。CKD273作为一种用于早期检测CKD的诊断测试已商业化,目前正在一项多中心随机临床试验(PRIORITY)中用于患者分层。最近,根据牛津循证医学和南安普顿牛津检索团队的指南对CKD273分类器的有效性进行了评估,美国食品药品监督管理局发布了支持CKD273的信函。在本文中,我们回顾了目前发表的关于CKD273的证据以及实施过程中面临的挑战。目前,定义一个可能的替代早期终点并结合CKD273作为患者分层的生物标志物,似乎是最有前景的策略,能够促使在干预仍有效的早期阶段开发出有效的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ca1/5499684/8e7d1e4528a1/sfx002f1.jpg

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