Systematic review: Association between circulating microRNA expression & stroke

Author:

Fullerton Josie L1,Thomas Josephine M23ORCID,Gonzalez-Trueba Laura1,Trivett Cara1ORCID,van Kralingen Josie C1,Allan Stuart M23ORCID,Quinn Terence J1ORCID,Work Lorraine M1ORCID

Affiliation:

1. Institute of Cardiovascular & Medical Science, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK

2. Division of Neuroscience & Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine & Health, University of Manchester, UK

3. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Group, & University of Manchester, Manchester, UK

Abstract

This systematic review aimed to establish the range and quality of clinical and preclinical evidence supporting the association of individual microRNAs, and the use of microRNA expression in the diagnosis and prognosis of ischaemic or haemorrhagic stroke. Electronic databases were searched from 1993 to October 2021, using key words relevant to concepts of stroke and microRNA. Studies that met specific inclusion and exclusion criteria were selected for data extraction. To minimise erroneous associations, findings were restricted to microRNAs reported to change in more than two independent studies. Of the papers assessed, 155 papers reported a change in microRNA expression observed in more than two independent studies. In ischaemic studies, two microRNAs were consistently differentially expressed in clinical samples (miR-29b & miR-146a) and four were altered in preclinical samples (miR-137, miR-146a, miR-181b & miR-223-3p). Across clinical and preclinical haemorrhagic studies, four microRNAs were downregulated consistently (miR-26a, miR-126, miR-146a & miR-155). Across included studies, miR-126 and miR-146a were the only two microRNAs to be differentially expressed in clinical and preclinical cohorts following ischaemic or haemorrhagic stroke. Further studies, employing larger populations with consistent methodologies, are required to validate the true clinical value of circulating microRNAs as biomarkers of ischaemic and haemorrhagic stroke.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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