Evidence map›Paper›PMID 38457375›Full record

ArticleThe international journal of neuropsychopharmacology2024

Profiling Small RNA From Brain Extracellular Vesicles in Individuals With Depression.

Pascal Ibrahim, Ryan Denniston, Haruka Mitsuhashi, Jennie Yang, Laura M Fiori, Dariusz Żurawek, Naguib Mechawar, Corina Nagy, Gustavo Turecki

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. The role ofEpigenetics · 2026
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  5. Plasma miRNA Profiles in Chronically Treated Bipolar Disorder Patients: A Case-Control Study.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Pascal IbrahimIntegrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Ryan DennistonMcGill Group for Suicide Studies, Douglas Mental Health University Institute, Verdun, Quebec, Canada.
Haruka MitsuhashiIntegrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Jennie YangMcGill Group for Suicide Studies, Douglas Mental Health University Institute, Verdun, Quebec, Canada.
Laura M FioriMcGill Group for Suicide Studies, Douglas Mental Health University Institute, Verdun, Quebec, Canada.ORCID 0000-0002-6840-471X
Dariusz ŻurawekMcGill Group for Suicide Studies, Douglas Mental Health University Institute, Verdun, Quebec, Canada.
Naguib MechawarIntegrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Corina NagyIntegrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.ORCID 0000-0003-1439-0129
Gustavo TureckiIntegrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada.
Douglas Mental Health University Institute · CA

Funding

Canadian Institute of Health Research FDN148374
6 · The paper itself

Abstract

backgroundMajor depressive disorder (MDD) is a leading cause of disability with significant mortality risk. Despite progress in our understanding of the etiology of MDD, the underlying molecular changes in the brain remain poorly understood. Extracellular vesicles (EVs) are lipid-bound particles that can reflect the molecular signatures of the tissue of origin. We aimed to optimize a streamlined EV isolation protocol from postmortem brain tissue and determine whether EV RNA cargo, particularly microRNAs (miRNAs), have an MDD-specific profile.

methodsEVs were isolated from postmortem human brain tissue. Quality was assessed using western blots, transmission electron microscopy, and microfluidic resistive pulse sensing. EV RNA was extracted and sequenced on Illumina platforms. Functional follow-up was performed in silico.

resultsQuality assessment showed an enrichment of EV markers, as well as a size distribution of 30 to 200 nm in diameter, and no contamination with cellular debris. Small RNA profiling indicated the presence of several RNA biotypes, with miRNAs and transfer RNAs being the most prominent. Exploring miRNA levels between groups revealed decreased expression of miR-92a-3p and miR-129-5p, which was validated by qPCR and was specific to EVs and not seen in bulk tissue. Finally, in silico functional analyses indicate potential roles for these 2 miRNAs in neurotransmission and synaptic plasticity.

conclusionWe provide a streamlined isolation protocol that yields EVs of high quality that are suitable for molecular follow-up. Our findings warrant future investigations into brain EV miRNA dysregulation in MDD.

Indexed as

Extracellular VesiclesMajor Depressive DisorderMicroRNAsBrainDepressionHumansMicroRNAsMirn129 microRNA, humandepressionExtracellular vesiclesmiRNAsize exclusion chromatographyultracentrifugation

Identifiers

PMID38457375
PMCPMC10946232
OpenAlexW4392613748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.