Urine and plasma metabolites predict the development of diabetic nephropathy in individuals with Type 2 diabetes mellitus

被引:136
作者
Pena, M. J. [1 ]
Heerspink, H. J. Lambers [1 ]
Hellemons, M. E. [1 ]
Friedrich, T. [2 ]
Dallmann, G. [2 ]
Lajer, M. [3 ]
Bakker, S. J. L. [4 ]
Gansevoort, R. T. [4 ]
Rossing, P. [3 ,5 ,6 ]
de Zeeuw, D. [1 ]
Roscioni, S. S. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharmacol, Groningen, Netherlands
[2] Biocrates Life Sci AG, Innsbruck, Austria
[3] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[4] Univ Groningen, Univ Med Ctr Groningen, Div Nephrol, NL-9713 AV Groningen, Netherlands
[5] Univ Aarhus, Aarhus, Denmark
[6] Univ Copenhagen, Ctr Basic Metab Res, Copenhagen, Denmark
关键词
CHRONIC KIDNEY-DISEASE; ALBUMIN EXCRETION; METABOLOMICS; REVEALS; MICROALBUMINURIA; HYPERTENSION; INFLAMMATION; DYSFUNCTION; BIOMARKERS; MECHANISM;
D O I
10.1111/dme.12447
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Early detection of individuals with Type 2 diabetes mellitus or hypertension at risk for micro- or macroalbuminuria may facilitate prevention and treatment of renal disease. We aimed to discover plasma and urine metabolites that predict the development of micro-or macroalbuminuria. Methods Patients with Type 2 diabetes (n = 90) and hypertension (n = 150) were selected from the community-cohort 'Prevention of REnal and Vascular End-stage Disease' (PREVEND) and the Steno Diabetes Center for this case-control study. Cases transitioned in albuminuria stage (from normo- to microalbuminuria or micro-to macroalbuminuria). Controls, matched for age, gender, and baseline albuminuria stage, remained in normo- or microalbuminuria stage during follow-up. Median follow-up was 2.9 years. Metabolomics were performed on plasma and urine. The predictive performance of a metabolite for albuminuria transition was assessed by the integrated discrimination index. Results In patients with Type 2 diabetes with normoalbuminuria, no metabolites discriminated cases from controls. In patients with Type 2 diabetes with microalbuminuria, plasma histidine was lower (fold change = 0.87, P = 0.02) and butenoylcarnitine was higher (fold change = 1.17, P = 0.007) in cases vs. controls. In urine, hexose, glutamine and tyrosine were lower in cases vs. controls (fold change = 0.20, P < 0.001; 0.32, P < 0.001; 0.51, P = 0.006, respectively). Adding the metabolites to a model of baseline albuminuria and estimated glomerular filtration rate metabolites improved risk prediction for macroalbuminuria transition (plasma integrated discrimination index = 0.28, P < 0.001; urine integrated discrimination index = 0.43, P < 0.001). These metabolites did not differ between hypertensive cases and controls without Type 2 diabetes. Conclusions Type 2 diabetes-specific plasma and urine metabolites were discovered that predict the development of macroalbuminuria beyond established renal risk markers. These results should be confirmed in a large, prospective cohort.
引用
收藏
页码:1138 / 1147
页数:10
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