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Published on: June 15, 2018
miRNAs in Uremic Cardiomyopathy: A Comprehensive Review
Mario D'Agostino1, Davide Mauro1, Mariateresa Zicarelli1
1Nephrology and Dialysis Unit, Department of Medical and Surgical Sciences, University "Magna-Graecia" of Catanzaro, Viale Europa SNC, 88100 Catanzaro, Italy.
Insights
MicroRNAs (miRNAs) are implicated in uremic cardiomyopathy (UCM), a complication in chronic kidney disease (CKD). Research suggests miRNAs may offer new diagnostic and therapeutic strategies for this condition.
Area of Science:
- Cardiology
- Nephrology
- Molecular Biology
Background:
- Uremic Cardiomyopathy (UCM) is a severe complication in chronic kidney disease (CKD) and End-Stage Kidney Disease (ESKD) patients.
- UCM involves myocardial fibrosis, hypertrophy, and diastolic dysfunction with unclear mechanisms.
- Micro-RNAs (miRNAs) are key regulators of cellular processes and are implicated in various diseases.
Purpose of the Study:
- To review the biological and clinical significance of miRNAs in UCM.
- To explore the role of miRNAs in UCM pathogenesis, including cardiac remodeling and fibrosis.
- To assess the potential of miRNAs as therapeutic targets and biomarkers for UCM.
Main Methods:
- Literature review of experimental and clinical evidence on miRNAs in UCM.
- Analysis of miRNA involvement in pathways related to ventricular hypertrophy and fibrosis.
- Evaluation of preliminary findings on miRNA-based diagnostics and therapeutics.
Main Results:
- Evidence confirms miRNA involvement in pathways driving UCM's ventricular hypertrophy and fibrosis.
- Preliminary data suggests potential for miRNA-targeted therapies to mitigate cardiac damage.
- Early clinical findings indicate circulating miRNAs may serve as UCM biomarkers.
Conclusions:
- miRNAs play a significant role in the development and progression of UCM.
- Targeting specific miRNAs holds promise for future UCM treatments.
- Circulating miRNAs may become valuable tools for UCM diagnosis and prognosis.
Abstract:
Uremic Cardiomyopathy (UCM) is an irreversible cardiovascular complication that is highly pervasive among chronic kidney disease (CKD) patients, particularly in End-Stage Kidney Disease (ESKD) individuals undergoing chronic dialysis. Features of UCM are an abnormal myocardial fibrosis, an asymmetric ventricular hypertrophy with subsequent diastolic dysfunction and a complex and multifactorial pathogenesis where underlying biological mechanisms remain partly undefined. In this paper, we reviewed the key evidence available on the biological and clinical significance of micro-RNAs (miRNAs) in UCM. miRNAs are short, noncoding RNA molecules with regulatory functions that play a pivotal role in myriad basic cellular processes, such as cell growth and differentiation. Deranged miRNAs expression has already been observed in various diseases, and their capacity to modulate cardiac remodeling and fibrosis under either physiological or pathological conditions is well acknowledged. In the context of UCM, robust experimental evidence confirms a close involvement of some miRNAs in the key pathways that are known to trigger or worsen ventricular hypertrophy or fibrosis. Moreover, very preliminary findings may set the stage for therapeutic interventions targeting specific miRNAs for ameliorating heart damage. Finally, scant but promising clinical evidence may suggest a potential future application of circulating miRNAs as diagnostic or prognostic biomarkers for improving risk stratification in UCM as well.
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MicroRNAs

