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Differential Pattern of Circulating MicroRNA Expression in Patients with Intracranial Atherosclerosis
Marine M Tanashyan1, Anton A Raskurazhev1, Alla A Shabalina1
1Research Center of Neurology, Moscow 125367, Russia.
Biomedicines
|February 26, 2025
Summary
Intracranial atherosclerosis (ICAS) shows a distinct epigenetic profile compared to extracranial atherosclerosis, with specific microRNAs linked to stroke mechanisms. This highlights the need to differentiate between ICAS and extracranial-only atherosclerosis (ECAS) in future research.
Area of Science:
- Cardiovascular Biology
- Epigenetics
- Neuroscience
Background:
- Intracranial atherosclerosis (ICAS) is a significant cause of ischemic stroke.
- Limited research exists on the epigenetic regulation of ICAS.
- Hypothesis: Extracranial atherosclerosis differs from ICAS due to anatomical/functional variations, explaining clinical variability.
Purpose of the Study:
- To investigate the differential expression of specific microRNAs (miRNAs) in patients with carotid stenosis.
- To explore the potential epigenetic distinctions between ICAS and extracranial atherosclerosis (ECAS).
- To identify miRNA signatures associated with atherogenic mechanisms and stroke symptoms in ICAS.
Main Methods:
- Selected miRNAs involved in atherogenesis for analysis.
- Measured plasma levels of selected miRNAs in patients with >50% carotid stenosis.
- Included patients with and without ICAS, analyzing differences in miRNA expression.
Main Results:
- Identified a distinct circulating miRNA expression pattern in ICAS patients.
- Observed overexpression of miR-712/205-5p, miR-106b-5p, miR-146a-5p, miR-200c-5p, miR-532-3p, and miR-126-3p in ICAS.
- Found underexpression of miR-712/205-3p and miR-100-3p in ICAS, linked to various atherogenic pathways.
- Noted significant upregulation of miR-712/205-3p and miR-146a-5p in symptomatic ICAS patients.
Conclusions:
- ICAS exhibits a unique epigenetic profile concerning circulating miRNA expression compared to ECAS.
- Ischemic stroke in ICAS may involve distinct pathophysiologic mechanisms.
- Specific miRNAs, like miR-712/205, may play a greater role in ICAS, potentially due to arterial differences.
- Distinguishing between ICAS and ECAS is crucial for future epigenetic studies of atherogenesis.

