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, Noutsou Marina, Ortiz Alberto, Persson Frederik, Petrie John R, Roob Johannes M, Rossing Peter, Ruggenenti Piero, Rychlik Ivan, Serra Andreas L, Snell-Bergeon Janet, Spasovski Goce, Stojceva-Taneva Olivera, Trillini Matias, von der Leyen Heiko, Winklhofer-Roob Brigitte M, Zürbig Petra, Jankowski Joachim
Mosaiques Diagnostics GmbH, Hanover, Germany Charité-Universitaetsmedizin Berlin, Medizinische Klinik IV, Berlin, Germany.
Mosaiques Diagnostics GmbH, Hanover, Germany Institut National de la Santé et de la Recherche Médicale (INSERM), U1048, Institut of Cardiovascular and Metabolic Disease, Toulouse, France Université Toulouse III Paul-Sabatier, Toulouse, France.
Nephrol Dial Transplant. 2014 Aug;29(8):1563-70. doi: 10.1093/ndt/gfu039. Epub 2014 Mar 2.
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.
糖尿病肾病(DN)是糖尿病主要的晚期并发症之一。虽然有旨在减缓DN进展的治疗方法,但目前缺乏早期明确检测DN进展的方法。“基于尿蛋白质组分类器(CKD273)对2型糖尿病伴正常白蛋白尿患者早期糖尿病肾病进行蛋白质组学预测及肾素 - 血管紧张素 - 醛固酮系统抑制预防”试验(PRIORITY)旨在评估使用基于尿蛋白质组的分类器(CKD273)对2型糖尿病(T2D)患者进行DN的早期检测。
在这项近期启动的PRIORITY试验的辅助研究中,我们旨在首次在多中心(9个不同机构,提供165例T2D患者的样本)前瞻性研究中验证CKD273分类器。此外,我们还研究了样本容器、年龄和性别对CKD273分类器的影响。
我们观察到不同中心的CKD273分类评分具有高度一致性,曲线下面积范围为0.95至1.00。该分类器与年龄(测试范围为16 - 89岁)和性别无关。此外,使用不同的尿液储存容器不会影响分类评分。对分类器中各个肽段在九个不同中心的分布分析表明,血液来源和细胞外基质蛋白的片段是最一致被发现的。
我们首次在多中心前瞻性研究中验证了这种基于尿蛋白质组的分类器,并表明CKD273分类器适用于PRIORITY试验。