4.6 Article

Multicentre prospective validation of a urinary peptidome-based classifier for the diagnosis of type 2 diabetic nephropathy

期刊

NEPHROLOGY DIALYSIS TRANSPLANTATION
卷 29, 期 8, 页码 1563-1570

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfu039

关键词

biomarkers; chronic kidney disease; diabetic nephropathy; diagnosis; urine proteomics

资金

  1. EU through PRIORITY [HEALTH-F2-2011-279277]
  2. EU through SysKID [HEALTH-F2-2009-241544]
  3. EU through PREDICTIONS [FP6-LIFESCIHEALTH-CT-2005-018733]
  4. EU from FP7-PEOPLE-IAPP program [GA 251368]
  5. Federal Ministry of Economics and Technology [KF2120002FR9]
  6. Fondo de Investigacion Sanitaria (FIS)
  7. region Midi-Pyrenees

向作者/读者索取更多资源

Diabetic nephropathy (DN) is one of the major late complications of diabetes. Treatment aimed at slowing down the progression of DN is available but methods for early and definitive detection of DN progression are currently lacking. The 'Proteomic prediction and Renin angiotensin aldosterone system Inhibition prevention Of early diabetic nephRopathy In TYpe 2 diabetic patients with normoalbuminuria trial' (PRIORITY) aims to evaluate the early detection of DN in patients with type 2 diabetes (T2D) using a urinary proteome-based classifier (CKD273). In this ancillary study of the recently initiated PRIORITY trial we aimed to validate for the first time the CKD273 classifier in a multicentre (9 different institutions providing samples from 165 T2D patients) prospective setting. In addition we also investigated the influence of sample containers, age and gender on the CKD273 classifier. We observed a high consistency of the CKD273 classification scores across the different centres with areas under the curves ranging from 0.95 to 1.00. The classifier was independent of age (range tested 16-89 years) and gender. Furthermore, the use of different urine storage containers did not affect the classification scores. Analysis of the distribution of the individual peptides of the classifier over the nine different centres showed that fragments of blood-derived and extracellular matrix proteins were the most consistently found. We provide for the first time validation of this urinary proteome-based classifier in a multicentre prospective setting and show the suitability of the CKD273 classifier to be used in the PRIORITY trial.

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