MicroRNA Biomarkers and Platelet Reactivity

Author:

Sunderland Nicholas1,Skroblin Philipp1,Barwari Temo1,Huntley Rachael P.1,Lu Ruifang1,Joshi Abhishek1,Lovering Ruth C.1,Mayr Manuel1

Affiliation:

1. From the King’s British Heart Foundation Centre, King’s College London, United Kingdom (N.S., P.S., T.B., R.L., A.J., M.M.); and Centre for Cardiovascular Genetics, Institute of Cardiovascular Science, University College London, United Kingdom (R.P.H., R.C.L.).

Abstract

Over the last few years, several groups have evaluated the potential of microRNAs (miRNAs) as biomarkers for cardiometabolic disease. In this review, we discuss the emerging literature on the role of miRNAs and other small noncoding RNAs in platelets and in the circulation, and the potential use of miRNAs as biomarkers for platelet activation. Platelets are a major source of miRNAs, YRNAs, and circular RNAs. By harnessing multiomics approaches, we may gain valuable insights into their potential function. Because not all miRNAs are detectable in the circulation, we also created a gene ontology annotation for circulating miRNAs using the gene ontology term extracellular space as part of blood plasma. Finally, we share key insights for measuring circulating miRNAs. We propose ways to standardize miRNA measurements, in particular by using platelet-poor plasma to avoid confounding caused by residual platelets in plasma or by adding RNase inhibitors to serum to reduce degradation. This should enhance comparability of miRNA measurements across different cohorts. We provide recommendations for future miRNA biomarker studies, emphasizing the need for accurate interpretation within a biological and methodological context.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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