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Small Extracellular Vesicles in Alcohol Use Disorders: A Scoping Review
Consortium Psychiatricum
|July 17, 2026
Summary
Small extracellular vesicles (sEVs) show distinct profiles in alcohol use disorders, differing in lipids, proteins, and microRNAs. These changes are linked to inflammation, highlighting sEVs as potential biomarkers for alcohol-related conditions.
Area of Science:
- Biochemistry
- Molecular Biology
- Public Health
Background:
- Alcohol use disorder (AUD) presents a major global health challenge with incompletely understood pathophysiology.
- Identifying reliable biomarkers for AUD remains a critical unmet need.
- Previous studies on small extracellular vesicles (sEVs) in AUD have yielded heterogeneous results, lacking systematic quality assessment.
Purpose of the Study:
- To systematically review and synthesize findings on the molecular profiles of sEVs in individuals with alcohol use disorders.
- To assess the methodological quality of existing research in this area.
Main Methods:
- A systematic literature search was conducted in MEDLINE and Scopus databases.
- Included studies focused on sEV profiles in AUD, analyzing lipid profiles, protein profiles, and signaling molecules.
- Methodological quality was evaluated using an adapted Newcastle-Ottawa Scale for extracellular vesicle research.
Main Results:
- Ten studies were included, all employing cross-sectional designs with small cohorts.
- Significant alterations in sEV lipid and protein profiles were observed in individuals with AUD compared to controls.
- Specific microRNAs (e.g., decreased hsa-miR-144-5p, increased miR-30a-5p) and inflammatory markers were differentially expressed, predominantly linked to inflammation regulation.
Conclusions:
- sEVs exhibit altered lipid, protein, and microRNA profiles in alcohol use disorders.
- These alterations are significantly associated with the regulation of systemic inflammation.
- Future research should employ prospective designs with repeated measurements to elucidate the role of sEVs in AUD pathophysiology and inflammation.

