ReviewMolecular neurobiology2026
The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.
Review in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Liquid biopsy is emerging as a powerful approach for less invasive biomarker discovery, with extracellular vesicles (EVs) in cerebrospinal fluid (CSF) showing promise for the assessment of central nervous system (CNS) disorders without actual tissue biopsy and as a complement to imaging techniques. EVs carry molecular cargo such as proteins, nucleic acids, and lipids that mirror those at the tissue of origin, offering unique opportunities to quantify disease-related changes in biomarkers. Compared with plasma-derived EVs, those from CSF provide more direct insights into the CNS because of direct shedding of brain EVs to CSF and bypass of confounding factors involving entry to systemic circulation. Despite this potential, translation into clinical practice is limited by challenges such as low yields, purity concerns, and lack of standardized isolation protocols. Addressing these difficulties, alongside integrating multiomics approaches, will advance our understanding of EV molecular cargo and their functional roles in CNS diseases. Over time, CSF-derived EVs could become the new driver of precision medicine in neurology, offering biologic insight for both diagnostic and therapeutic applications. This perspective provides a critical evaluation of the current status of EV-based liquid biopsy in CSF and offers recommendations for future research and clinical translation of data from CSF-derived EVs, highlighting their potential to inform physiologically based pharmacokinetic (PBPK) models. This state-of-the-art article evaluates existing evidence and highlights key knowledge gaps.
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What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.