Characteristics of high- and low-risk individuals in the PRIORITY study: urinary proteomics and mineralocorticoid receptor antagonism for prevention of diabetic nephropathy in Type 2 diabetes

N. Tofte*, M. Lindhardt, K. Adamova, J. Beige, J. W. J. Beulens, A. L. Birkenfeld, G. Currie, C. Delles, I. Dimos, L. Francova, M. Frimodt-Moller, P. Girman, R. Goeke, T. Havrdova, A. Kooy, H. Mischak, G. Navis, G. Nijpels, M. Noutsou, A. OrtizA. Parvanova, F. Persson, P. L. Ruggenenti, F. Rutters, I. Rychlik, G. Spasovski, M. Speeckaert, M. Trillini, H. von der Leyen, P. Rossing

*Bijbehorende auteur voor dit werk

OnderzoeksoutputAcademicpeer review

24 Citaten (Scopus)

Samenvatting

AimTo compare clinical baseline data in individuals with Type 2 diabetes and normoalbuminuria, who are at high or low risk of diabetic kidney disease based on the urinary proteomics classifier CKD273.

MethodsWe conducted a prospective, randomized, double-blind, placebo-controlled international multicentre clinical trial and observational study in participants with Type 2 diabetes and normoalbuminuria, stratified into high- or low-risk groups based on CKD273 score. Clinical baseline data for the whole cohort and stratified by risk groups are reported. The associations between CKD273 and traditional risk factors for diabetic kidney disease were evaluated using univariate and logistic regression analysis.

ResultsA total of 1777 participants from 15 centres were included, with 12.3% of these having a high-risk proteomic pattern. Participants in the high-risk group (n=218), were more likely to be men, were older, had longer diabetes duration, a lower estimated GFR and a higher urinary albumin:creatinine ratio than those in the low-risk group (n=1559, P

ConclusionsIn this population of individuals with Type 2 diabetes and normoalbuminuria, traditional diabetic kidney disease risk factors differed slightly between participants at high risk and those at low risk of diabetic kidney disease, based on CKD273. These data suggest that CKD273 may provide additional prognostic information over and above the variables routinely available in the clinic. Testing the added value will be subject to our ongoing study. (European Union Clinical Trials Register: EudraCT 2012-000452-34 and Clinicaltrials.gov: NCT02040441).

Originele taal-2English
Pagina's (van-tot)1375-1382
Aantal pagina's8
TijdschriftDiabetic Medicine
Volume35
Nummer van het tijdschrift10
DOI's
StatusPublished - okt.-2018

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