Circulating miRNA 122-5p Expression Predicts Mortality and Cardiovascular Events in Chronic Hemodialysis Patients: A Multicentric, Pilot, Prospective Study

Author:

Duni Anila1,Greco Marta23ORCID,Presta Pierangela4,Arena Roberta4,Pappas Ethymios5,Lakkas Lampros6,Naka Katerina K.6ORCID,Brunetti Antonio2ORCID,Foti Daniela Patrizia37ORCID,Andreucci Michele24ORCID,Coppolino Giuseppe24ORCID,Dounousi Evangelia1ORCID,Bolignano Davide48

Affiliation:

1. Department of Nephrology, School of Medicine, University of Ioannina, 45110 Ioannina, Greece

2. Department of Health Sciences, Magna Graecia University, 88100 Catanzaro, Italy

3. Clinical Pathology Lab., Magna Graecia University, 88100 Catanzaro, Italy

4. Nephrology and Dialysis Unit, Magna Graecia University, 88100 Catanzaro, Italy

5. Hemodialysis Unit, General Hospital of Filiates, 46300 Filiates, Greece

6. Second Department of Cardiology, University Hospital of Ioannina, 45500 Ioannina, Greece

7. Department of Experimental and Clinical Medicine, Magna Graecia University, 88100 Catanzaro, Italy

8. Department of Medical and Surgical Sciences, Magna Graecia University, 88100 Catanzaro, Italy

Abstract

Background: Despite patients undergoing chronic hemodialysis (HD) being notoriously prone to adverse cardiovascular (CV) events, risk prediction in this population remains challenging. miRNA 122-5p, a short, non-coding RNA predominantly involved in lipid and carbohydrate metabolism, has recently been related to the onset and progression of CV disease. Methods: We run a pilot, multicenter, longitudinal, observational study to evaluate the clinical significance and prognostic usefulness of circulating miRNA 122-5p in a multicentric cohort of 74 individuals on maintenance HD. Results: Patients displayed lower circulating miRNA 122-5p as compared to healthy controls (p = 0.004). At correlation analyses, ALT (β = 0.333; p = 0.02), E/e’ (β = 0.265; p = 0.02) and CRP (β = −0.219; p = 0.041) were independent predictors of miRNA 122-5p levels. During a median follow-up of 22 months (range of 1–24), 30 subjects (40.5%) experienced a composite endpoint of all-cause mortality and fatal/non-fatal CV events. Baseline circulating miRNA 122-5p was higher in these subjects (p = 0.01) and it predicted a significantly higher risk of endpoint occurrence (Kaplan–Meier crude HR 3.192; 95% CI 1.529–6.663; p = 0.002; Cox regression adjusted HR 1.115; 95% CI 1.009–1.232; p = 0.03). Conclusions: Altered miRNA 122-5p levels in HD patients may reflect hepatic and CV damage and may impart important prognostic information for improving CV risk prediction in this particular setting.

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

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