Improved cardiovascular risk prediction in patients with end-stage renal disease on hemodialysis using machine learning modeling and circulating microribonucleic acids

To test whether novel biomarkers, such as microribonucleic acids (miRNAs), and nonstandard predictive models, such as decision tree learning, provide useful information for medical decision-making in patients on hemodialysis (HD). Samples from patients with end-stage renal disease receiving HD inclu...

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Veröffentlicht in:Theranostics 2020-01, Vol.10 (19), p.8665-8676
Hauptverfasser: de Gonzalo-Calvo, David, Martínez-Camblor, Pablo, Bär, Christian, Duarte, Kevin, Girerd, Nicolas, Fellström, Bengt, Schmieder, Roland E, Jardine, Alan G, Massy, Ziad A, Holdaas, Hallvard, Rossignol, Patrick, Zannad, Faiez, Thum, Thomas
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Sprache:eng
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Zusammenfassung:To test whether novel biomarkers, such as microribonucleic acids (miRNAs), and nonstandard predictive models, such as decision tree learning, provide useful information for medical decision-making in patients on hemodialysis (HD). Samples from patients with end-stage renal disease receiving HD included in the AURORA trial were investigated (n=810). The study included two independent phases: phase I (matched cases and controls, n=410) and phase II (unmatched cases and controls, n=400). The composite endpoint was cardiovascular death, nonfatal myocardial infarction or nonfatal stroke. miRNA quantification was performed using miRNA sequencing and RT-qPCR. The CART algorithm was used to construct regression tree models. A bagging-based procedure was used for validation. In phase I, miRNA sequencing in a subset of samples (n=20) revealed miR-632 as a candidate (fold change=2.9). miR-632 was associated with the endpoint, even after adjusting for confounding factors (HR from 1.43 to 1.53). These findings were not reproduced in phase II. Regression tree models identified eight patient subgroups with specific risk patterns. miR-186-5p and miR-632 entered the tree by redefining two risk groups: patients older than 64 years and with hsCRP
ISSN:1838-7640
1838-7640
DOI:10.7150/thno.46123