Evidence map›Paper›PMID 36009857›Full record

ReviewBiology2022

Mechanisms and Biomarker Potential of Extracellular Vesicles in Stroke.

Nikita Ollen-Bittle, Austyn D Roseborough, Wenxuan Wang, Jeng-Liang D Wu, Shawn N Whitehead

Abstract readReview
In one paragraph

Review in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Extracellular Vesicles as a Potential Therapy for Stroke.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Plasma/Serum Proteomics based on Mass Spectrometry.Protein and peptide letters · 2024
    Review
  15. Review
  16. New Biomarkers for Cardiovascular Disease.Texas Heart Institute journal · 2023
    Review
  17. Article
  18. Review
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

5 authors.

Nikita Ollen-BittleVulnerable Brain Laboratory, Department of Anatomy and Cell Biology, Western University, London, ON N6A 5C1, Canada.
Austyn D RoseboroughVulnerable Brain Laboratory, Department of Anatomy and Cell Biology, Western University, London, ON N6A 5C1, Canada.
Wenxuan WangVulnerable Brain Laboratory, Department of Anatomy and Cell Biology, Western University, London, ON N6A 5C1, Canada.
Jeng-Liang D WuVulnerable Brain Laboratory, Department of Anatomy and Cell Biology, Western University, London, ON N6A 5C1, Canada.
Shawn N WhiteheadVulnerable Brain Laboratory, Department of Anatomy and Cell Biology, Western University, London, ON N6A 5C1, Canada.

Funding

CIHR 202104PJT-461038Natural Sciences and Engineering Research Council RGPIN-2019-04742
6 · The paper itself

Abstract

Stoke is a prevalent and devastating neurologic condition with limited options for therapeutic management. Since brain tissue is rarely accessible clinically, peripheral biomarkers for the central nervous system's (CNS's) cellular response to stroke may prove critical for increasing our understanding of stroke pathology and elucidating novel therapeutic targets. Extracellular vesicles (EVs) are cell-derived, membrane-enclosed vesicles secreted by all cell types within the CNS that can freely pass the blood-brain barrier (BBB) and contain unique markers and content linked to their cell of origin. These unique qualities make brain-derived EVs novel candidates for non-invasive blood-based biomarkers of both cell specificity and cell physiological state during the progression of stroke and recovery. While studies are continuously emerging that are assessing the therapeutic potential of EVs and profiling EV cargo, a vast minority of these studies link EV content to specific cell types. A better understanding of cell-specific EV release during the acute, subacute, and chronic stages of stroke is needed to further elucidate the cellular processes responsible for stroke pathophysiology. Herein, we outline what is known about EV release from distinct cell types of the CNS during stroke and the potential of these EVs as peripheral biomarkers for cellular function in the CNS during stroke.

Indexed as

biomarkerscellular biologydementiadiseasesextracellular vesicles (EVs)inflammationstroke

Identifiers

PMID36009857
PMCPMC9405035

What Socratic 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 Socratic graph.