4.6 Article

Liver-specific microRNA-122 as prognostic biomarker in patients with chronic systolic heart failure

Journal

INTERNATIONAL JOURNAL OF CARDIOLOGY
Volume 303, Issue -, Pages 80-85

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2019.11.090

Keywords

Liver miR-122; miR-423; Chronic heart failure; Prognostic biomarker

Funding

  1. Anniversary Fund of Austrian National Bank grant [AP15688ONB]
  2. Association for the Promotion of Research in Arteriosclerosis, Thrombosis and Vascular Biology
  3. R&D K-Centre (COMET program-Competence Centers for Excellent Technologies) - Austrian Ministry for Transport, Innovation and Technology [CH/16/3/32406]
  4. Austrian Ministry for Digital and Economic Affairs
  5. federal state Tyrol
  6. federal state Salzburg
  7. federal state Vienna

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Background: Circulating microRNAs (miRs) have been proposed as potential diagnostic biomarkers in heart failure. Studies investigating the prognostic value of circulating miRs in patients with chronic systolic heart failure (HFrEF) are scarce. The aim of this study was to investigate the prognostic value of circulating miRs in patients with HFrEF. Methods and results: A pathway-focused microRNA array was performed in derivation case-control cohort of 40 patients with HFrEF who died during the follow-up (cases) and 36 survivors (controls). MicroRNA expression profiling revealed significant differential expression of miR-122, miR-126 and miR-423 between cases and controls. In a validation cohort, circulating levels of these 3 miRs were assessed using qPCR in 234 patients with HFrEF. Primary study endpoints were all-cause and cardiovascular mortality. During a median follow-up time of 3.2 years, 76 patients (32.5%) died. Only miR-122 and miR-423 were independent predictors of the primary endpoint with respective hazard ratios per increase of one standard deviation (HR per 1-SD) of 1.14 (95% CI: 1.02-1.29, p = 0.021) and 1.24 (95% CI: 1.09-1.41, p = 0.001). Adding miR-122 to multivariable model including clinical risk factors and NT-proBNP improved net reclassification index (NRI) by 40.4% (p = 0.004), whereas miR-423 improved NRI by 35.3% (p = 0.012). Adding miR-122, but not miR-423, to the same model improved Harrell's C index from 0.78 (95% CI: 0.73-0.83) to 0.81 (95% CI: 0.76-0.86, p = 0.030). Conclusion: CirculatingmiR-122 as a biomarker is predicting all-cause and cardiovascular mortality and improved risk stratification of HFrEF patients. Thus, miR-122 might be a new biomarker for risk assessment in HFrEF. Crown Copyright (C) 2019 Published by Elsevier B.V. All rights reserved.

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