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January 25, 2026Journal of Neurochemistry4 citations

Extracellular Vesicle‐Derived microRNAs as Fluid Biomarkers in Neurodegenerative Diseases: A Systematic Review

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AZAliyah ZamanSDSienna DrakeAFAlyson E. Fournier

Key Points

  • This review aims to assess the role of extracellular vesicle-derived microRNAs as biomarkers in neurodegenerative diseases.
  • Conducted a systematic search of the MEDLINE database for relevant studies.
  • Extracted miRNA expression data from 185 peer-reviewed publications.
  • Consolidated results to identify frequently dysregulated miRNAs across various neurodegenerative diseases.
  • Analyzed miRNA expression in cerebrospinal fluid and plasma compared to serum.
  • Identified key dysregulated miRNAs associated with multiple neurodegenerative diseases.
  • Noted consistent miRNA expression patterns in cerebrospinal fluid and plasma, but discrepancies in serum.
  • Highlighted specific miRNAs, including miR-143-3p and miR-9-5p, as potential biomarkers for neuropathology.

Abstract

ABSTRACT Given the absence of curative treatments for neurodegenerative diseases, early detection and therapeutic intervention are critical to slowing disease progression. Extracellular vesicles (EVs) have emerged as promising biomarkers for neurodegeneration, owing to their accessibility in bodily fluids and dynamic molecular cargo, including microRNAs (miRNAs). The last decade has seen accumulating evidence for miRNA dysregulation in circulating EVs from people with neurodegenerative diseases; however, assessing reproducibility between studies remains challenging, largely due to clinical and methodological heterogeneity. In this systematic review, we comprehensively searched the MEDLINE database for studies investigating miRNA expression in biofluids from people with neurodegenerative diseases. We extracted miRNA expression data from 185 peer‐reviewed publications, published until June of 2025, reporting altered miRNA levels in fluid‐derived EVs from people with neurodegenerative diseases. We consolidated results between studies to identify the most frequently dysregulated miRNAs across diseases, with a focus on Alzheimer's disease, Parkinson's disease, mild cognitive impairment, multiple sclerosis, amyotrophic lateral sclerosis, frontotemporal dementia, stroke, traumatic brain injury, and schizophrenia. Evaluating tissue specificity of frequently dysregulated miRNAs revealed enrichment of select miRNAs in the nervous system relative to blood and immune compartments. Summarizing miRNA regulation across biofluids emphasized consistencies between cerebrospinal fluid and plasma, but not serum. We highlight circulating miRNAs that may be reflective of neuropathology, including miR‐143‐3p, miR‐127‐3p, miR‐9‐5p, miR‐15a‐5p, and miR‐125b‐5p. Finally, we provide a repository of miRNA expression data from over 30 neurodegenerative conditions which can be exploited to further investigate miRNA regulation in diseases of interest. image

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Cite This Study

Zaman et al. (2026) studied this question.

synapsesocial.com/papers/6975b26ffeba4585c2d6df79https://doi.org/10.1111/jnc.70323
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