Related Experiment Video
Updated: Oct 16, 2025

Enrichment of Astrocyte-Derived Extracellular Vesicles from Human Plasma
Published on: August 3, 2022
Systematic Search for Novel Circulating Biomarkers Associated with Extracellular Vesicles in Alzheimer's Disease:
David Vogrinc1, Katja Goričar1, Tanja Kunej2
1Pharmacogenetics Laboratory, Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.
Abstract:
miRNAs play an important role in neurodegenerative diseases. Many miRNA-target gene interactions (MTI) have been experimentally confirmed and associated with Alzheimer's disease (AD). miRNAs may also be contained within extracellular vesicles (EVs), mediators of cellular communication and a potential source of circulating biomarkers in body fluids. Therefore, EV-associated miRNAs (EV-miRNAs) in peripheral blood could support earlier and less invasive AD diagnostics. We aimed to prioritize EV-related miRNA with AD-related genes and to identify the most promising candidates for novel AD biomarkers. A list of unique EV-miRNAs from the literature was combined with a known set of AD risk genes and enriched for MTI. Additionally, miRNAs associated with the AD phenotype were combined with all known target genes in MTI enrichment. Expression in different sample types was analyzed to identify AD-associated miRNAs with the greatest potential as AD circulating biomarkers. Four common MTI were observed between EV-miRNAs and AD-associated miRNAs: hsa-miR-375-APH1B, hsa-miR-107-CDC42SE2, hsa-miR-375-CELF2, and hsa-miR-107-IL6. An additional 61 out of 169 unique miRNAs (36.1%) and seven out of 84 unique MTI (8.3%), observed in the body fluids of AD patients, were proposed as very strong AD-circulating biomarker candidates. Our analysis summarized several potential novel AD biomarkers, but further studies are needed to evaluate their potential in clinical practice.
Insights
Extracellular vesicle-associated microRNAs (EV-miRNAs) show promise as Alzheimer
Area of Science:
- Neuroscience
- Genetics
- Biomarker Discovery
Background:
- MicroRNAs (miRNAs) are crucial in neurodegenerative diseases like Alzheimer's disease (AD).
- Extracellular vesicles (EVs) carry miRNAs, serving as potential circulating biomarkers in body fluids.
- EV-associated miRNAs (EV-miRNAs) in peripheral blood offer possibilities for early, less invasive AD diagnostics.
Purpose of the Study:
- To prioritize EV-related miRNAs interacting with AD-associated genes.
- To identify promising EV-miRNA candidates for novel Alzheimer's disease biomarkers.
Main Methods:
- Combined literature-derived EV-miRNAs with known AD risk genes, enriching for miRNA-target gene interactions (MTI).
- Integrated AD phenotype-associated miRNAs with known target genes for MTI enrichment.
- Analyzed miRNA expression in various sample types to identify potential circulating AD biomarkers.
Main Results:
- Identified four common MTI between EV-miRNAs and AD-associated miRNAs: hsa-miR-375-APH1B, hsa-miR-107-CDC42SE2, hsa-miR-375-CELF2, and hsa-miR-107-IL6.
- Proposed 61 out of 169 unique miRNAs (36.1%) and seven out of 84 unique MTI (8.3%) as strong AD-circulating biomarker candidates.
- Highlighted specific EV-miRNAs and MTI with potential diagnostic value for Alzheimer's disease.
Conclusions:
- The study identified several potential novel AD biomarkers from EV-miRNAs.
- These findings suggest EV-miRNAs could serve as valuable circulating biomarkers for Alzheimer's disease.
- Further research is necessary to validate these candidates for clinical application in AD diagnostics.
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