Title | A Novel Metabolic Signature To Predict the Requirement of Dialysis or Renal Transplantation in Patients with Chronic Kidney Disease. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Zacharias HU, Altenbuchinger M, Schultheiss UT, Samol C, Kotsis F, Poguntke I, Sekula P, Krumsiek J, Köttgen A, Spang R, Oefner PJ, Gronwald W |
Journal | J Proteome Res |
Volume | 18 |
Issue | 4 |
Pagination | 1796-1805 |
Date Published | 2019 Apr 05 |
ISSN | 1535-3907 |
Keywords | Aged, Female, Humans, Kidney Transplantation, Male, Metabolome, Metabolomics, Middle Aged, Models, Statistical, Predictive Value of Tests, Renal Dialysis, Renal Insufficiency, Chronic, Risk Assessment |
Abstract | Identification of chronic kidney disease patients at risk of progressing to end-stage renal disease (ESRD) is essential for treatment decision-making and clinical trial design. Here, we explored whether proton nuclear magnetic resonance (NMR) spectroscopy of blood plasma improves the currently best performing kidney failure risk equation, the so-called Tangri score. Our study cohort comprised 4640 participants from the German Chronic Kidney Disease (GCKD) study, of whom 185 (3.99%) progressed over a mean observation time of 3.70 ± 0.88 years to ESRD requiring either dialysis or transplantation. The original four-variable Tangri risk equation yielded a C statistic of 0.863 (95% CI, 0.831-0.900). Upon inclusion of NMR features by state-of-the-art machine learning methods, the C statistic improved to 0.875 (95% CI, 0.850-0.911), thereby outperforming the Tangri score in 94 out of 100 subsampling rounds. Of the 24 NMR features included in the model, creatinine, high-density lipoprotein, valine, acetyl groups of glycoproteins, and Ca-EDTA carried the highest weights. In conclusion, proton NMR-based plasma fingerprinting improved markedly the detection of patients at risk of developing ESRD, thus enabling enhanced patient treatment. |
DOI | 10.1021/acs.jproteome.8b00983 |
Alternate Journal | J Proteome Res |
PubMed ID | 30817158 |