Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect
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Updated: Jul 15, 2026

Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment
Published on: June 2, 2020
C Visconte1, M T Golia2, C Fenoglio3
1Department of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Abstract:
Extracellular vesicles (EVs) are mediators of cellular communication that can be released by almost all cell types in both physiological and pathological conditions and are present in most biological fluids. Such characteristics make them attractive in the research of biomarkers for age-related pathological conditions. Based on this, the aim of the present study was to examine the changes in EV concentration and size in the context of frailty, a geriatric syndrome associated with a progressive physical and cognitive decline. Specifically, total EVs and neural and microglial-derived EVs (NDVs and MDVs respectively) were investigated in plasma of frail and non-frail controls (CTRL), mild cognitive impairment (MCI) subjects, and in Alzheimer's disease (AD) patients. Results provided evidence that AD patients displayed diminished NDV concentration (3.61 × 109 ± 1.92 × 109 vs 7.16 × 109 ± 4.3 × 109 particles/ml) and showed high diagnostic performance. They are able to discriminate between AD and CTRL with an area under the curve of 0.80, a sensitivity of 78.95% and a specificity of 85.7%, considering the cut-off of 5.27 × 109 particles/ml. Importantly, we also found that MDV concentration was increased in frail MCI patients compared to CTRL (5.89 × 109 ± 3.98 × 109 vs 3.16 × 109 ± 3.04 × 109 particles/ml, P < 0.05) and showed high neurotoxic effect on neurons. MDV concentration discriminate frail MCI vs non-frail CTRL (AUC = 0.76) with a sensitivity of 80% and a specificity of 70%, considering the cut-off of 2.69 × 109 particles/ml. Altogether, these results demonstrated an alteration in NDV and MDV release during cognitive decline, providing important insight into the role of EVs in frailty status.
Insights
Extracellular vesicles (EVs) are key to cellular communication and show altered levels in Alzheimer's disease (AD) and frailty. Neural-derived EVs (NDVs) decrease in AD, while microglial-derived EVs (MDVs) increase in frail patients with mild cognitive impairment.
Area of Science:
- Gerontology and Neuroscience
- Cellular Biology and Biomarkers
Background:
- Extracellular vesicles (EVs) are crucial intercellular communicators found in biological fluids.
- Their role as biomarkers for age-related conditions, including frailty and cognitive decline, is under investigation.
- Frailty is a geriatric syndrome characterized by physical and cognitive deterioration.
Purpose of the Study:
- To investigate alterations in EV concentration and size in frail individuals, mild cognitive impairment (MCI) patients, and Alzheimer's disease (AD) patients.
- To specifically analyze neural-derived EVs (NDVs) and microglial-derived EVs (MDVs) in plasma samples.
- To assess the diagnostic potential of these EVs in distinguishing between patient groups and controls.
Main Methods:
- Plasma samples from frail individuals, non-frail controls (CTRL), MCI subjects, and AD patients were analyzed.
- Concentration and size of total EVs, NDVs, and MDVs were measured.
- Diagnostic performance metrics (AUC, sensitivity, specificity) were calculated for discriminating between groups.
Main Results:
- AD patients showed significantly diminished NDV concentrations, with high diagnostic performance for AD vs. CTRL (AUC=0.80).
- Frail MCI patients exhibited increased MDV concentrations compared to CTRL (P < 0.05), demonstrating a potential neurotoxic effect.
- MDV concentration effectively discriminated frail MCI from non-frail CTRL (AUC=0.76).
Conclusions:
- EVs, specifically NDVs and MDVs, show altered release patterns associated with cognitive decline and frailty.
- NDVs may serve as a biomarker for Alzheimer's disease.
- Increased MDVs in frail MCI patients suggest a role in neurotoxicity and cognitive impairment.
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