Journal
JOURNAL OF DIABETES AND ITS COMPLICATIONS
Volume 33, Issue 1, Pages 39-45Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jdiacomp.2018.09.019
Keywords
Diabetic kidney disease; Proteinuric phenotype; Non-proteinuric phenotype; Clinical features; Outcomes
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Funding
- National Key Research and Development Program [2016YFC1305405]
- National Natural Science Foundation of China [81641122]
- Northern/Pacific Universities Global Health Research Training consortium of National Institutes of Health [R25 TW009345]
- University of Michigan Health System and Peking University Health Sciences Center Joint Institute for Translational and Clinical Research [BMU20160466]
- interdisciplinary medicine Seed Fund of Peking University [BMU2018MX010]
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Background: Information regarding the clinical phenotypes of diabetic kidney disease (DKD) might guide better practice for clinicians. We aim to compare the clinical features and long-term outcomes of proteinuric and nonproteinuric phenotypes of DKD, based on a prospective cohort of Chinese population. Methods: Altogether 8811 Chinese participants with diabetes were included. Kidney function decline was defined as estimated glomerular filtration rate <60 mL/min.1.73 m(-2). The presence of proteinuria by urine dipstick test was further divided into micro-proteinuria (trace or 1+) and overt-proteinuria (>= 2+). Participants were then stratified into 5 groups: no DKD, isolated kidney function decline, isolated micro-proteinuria, isolated overtproteinuria, and proteinuria combined with kidney function decline. Outcomes include the first occurrence of composite cardiovascular events, end-stage renal disease (ESRD), and all-cause mortality. Main findings: After a median follow-up of 6.9 years, there were 646 composite cardiovascular events, 31 ESRD events, and 718 deaths. Isolated kidney function decline was only associated with the higher risk of ESRD (HRs 31.33 (95% CI 3.65-269.27)). Participants of overt-proteinuria and proteinuria combined with kidney function decline phenotypes were associated with increased risk of all predefined adverse outcomes. Conclusions: Proteinuric and non-proteinuric DKD phenotypes might follow different pathophysiological pathways, and result in heterogeneous clinical features and prognosis. (C) 2018 Elsevier Inc. All rights reserved.
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