Expansion of plasma MicroRNAs over the first month following human stroke

Author:

Edwardson Matthew A12ORCID,Shivapurkar Narayan3,Li James4,Khan Muhib56,Smith Jamal2,Giannetti Margot L2,Fan Ruzong4,Dromerick Alexander W12

Affiliation:

1. Department of Neurology, Georgetown University, Washington, DC, USA

2. Research Division, MedStar National Rehabilitation Hospital, Washington, DC, USA

3. Department of Medicine, Georgetown University, Washington, DC, USA

4. Department of Biostatistics, Bioinformatics, and Mathematics, Georgetown University, Washington, DC, USA

5. Spectrum Health, Grand Rapids, MI, USA

6. Michigan State University, College of Human Medicine, Grand Rapids, MI, USA

Abstract

Few have characterized miRNA expression during the transition from injury to neural repair and secondary neurodegeneration following stroke in humans. We compared expression of 754 miRNAs from plasma samples collected 5, 15, and 30 days post-ischemic stroke from a discovery cohort (n = 55) and 15-days post-ischemic stroke from a validation cohort (n = 48) to healthy control samples (n = 55 and 48 respectively) matched for age, sex, race and cardiovascular comorbidities using qRT-PCR. Eight miRNAs remained significantly altered across all time points in both cohorts including many described in acute stroke. The number of significantly dysregulated miRNAs more than doubled from post-stroke day 5 (19 miRNAs) to days 15 (50 miRNAs) and 30 (57 miRNAs). Twelve brain-enriched miRNAs were significantly altered at one or more time points (decreased expression, stroke versus controls: miR-107; increased expression: miR-99-5p, miR-127-3p, miR-128-3p, miR-181a-3p, miR-181a-5p, miR-382-5p, miR-433-3p, miR-491-5p, miR-495-3p, miR-874-3p, and miR-941). Many brain-enriched miRNAs were associated with apoptosis over the first month post-stroke whereas other miRNAs suggested a transition to synapse regulation and neuronal protection by day 30. These findings suggest that a program of decreased cellular proliferation may last at least 30 days post-stroke, and points to specific miRNAs that could contribute to neural repair in humans.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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