دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: Multicentre prospective validation of a urinary peptidome-based classifier for the diagnosis of type 2 diabetic nephropathy.
المؤلفون: Siwy, Justyna, Schanstra, Joost P., Argiles, Angel, Bakker, Stephan J.L., Beige, Joachim, Boucek, Petr, Brand, Korbinian, Delles, Christian, Duranton, Flore, Fernandez-Fernandez, Beatriz, Jankowski, Marie-Luise, Al Khatib, Mohammad, Kunt, Thomas, Lajer, Maria, Lichtinghagen, Ralf, Lindhardt, Morten, Maahs, David M, Mischak, Harald, Mullen, William, Navis, Gerjan
المصدر: Nephrology Dialysis Transplantation; Aug2014, Vol. 29 Issue 8, p1563-1570, 8p
مصطلحات موضوعية: DIABETIC nephropathies, DIABETES complications, EARLY diagnosis, DISEASE progression, LONGITUDINAL method, DIAGNOSIS, THERAPEUTICS
مستخلص: Background 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). Methods 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. Results 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. Conclusion 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. [ABSTRACT FROM PUBLISHER]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:09310509
DOI:10.1093/ndt/gfu039