Evidence map›Paper›PMID 35952764›Full record

ReviewExperimental neurology2022

Extracellular vesicles and Alzheimer's disease in the novel era of Precision Medicine: implications for disease progression, diagnosis and treatment.

Patrícia Gomes, Foteini Tzouanou, Konstantina Skolariki, Anastasia Vamvaka-Iakovou, Carlos Noguera-Ortiz, Katerina Tsirtsaki, Clarissa L Waites, Panagiotis Vlamos, Nuno Sousa, Bruno Costa-Silva and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in Experimental neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.2field-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

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

12 authors at 7 institutions in 3 countries.

Patrícia GomesLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Foteini TzouanouInstitute of Biosciences & Applications NCSR "Demokritos", Athens, Greece.
Konstantina SkolarikiDepartment of Informatics, Ionian University, Corfu, Greece.
Anastasia Vamvaka-IakovouLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal; Institute of Biosciences & Applications NCSR "Demokritos", Athens, Greece.
Carlos Noguera-OrtizLaboratory of Clinical Investigation, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Katerina TsirtsakiInstitute of Biosciences & Applications NCSR "Demokritos", Athens, Greece.
Clarissa L WaitesDepartment of Pathology and Cell Biology, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, NY, USA.
Panagiotis VlamosDepartment of Informatics, Ionian University, Corfu, Greece.
Nuno SousaLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Bruno Costa-SilvaSystems Oncology Group, Champalimaud Research, Champalimaud Centre for the Unknown, Av. Brasília, 1400-038 Lisbon, Portugal.
Dimitrios KapogiannisLaboratory of Clinical Investigation, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Ioannis SotiropoulosLife and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal; Institute of Biosciences & Applications NCSR "Demokritos", Athens, Greece. Electronic address: ioannis@med.uminho.pt.
University of Minho · PTIonian University · GRNational Centre of Scientific Research "Demokritos" · GRNational Institute on Aging · USChampalimaud Foundation · PTColumbia University Irving Medical Center · USInstitute of Biosciences & Applications

Funding

Studies in Dementia and Neurodegenerative DiseasesZIAAG000975 · NIA · NATIONAL INSTITUTE ON AGING · PI KAPOGIANNIS, DIMITRIOS · 2009 to 2025
$31.5M
Uncovering stress-induced mechanisms of Tau pathology in Alzheimer's diseaseRF1AG069941 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Clarissa Leigh Waites · 2020 to 2026
$5.5M
Extraceullar Vesicle Biomarkers for Prediction of Cognitive Decline, Ab and TAU Accumulation, and atrophy in Preclinical Alzheimer's DiseaseZIAAG000003 · NIA · NATIONAL INSTITUTE ON AGING · PI KAPOGIANNIS, DIMITRIOS · 2022 to 2025
$4.4M
Uncovering stress-induced mechanisms of Tau pathology in Alzheimer's diseaseR01AG069941 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WAITES, CLARISSA LEIGH · 2024 to 2024
$552k
Intramural NIH HHS Z99 AG999999Intramural NIH HHS ZIA AG000975NIA NIH HHS R01 AG069941NIA NIH HHS RF1 AG069941
6 · The paper itself

Abstract

Extracellular vesicles (EVs), secreted membranous nano-sized particles, are critical intercellular messengers participating in nervous system homeostasis, while recent evidence implicates EVs in Alzheimer's disease (AD) pathogenesis. Specifically, small EVs have been shown to spread toxic proteins, induce neuronal loss, and contribute to neuroinflammation and AD progression. On the other hand, EVs can reduce amyloid-beta deposition and transfer neuroprotective substances between cells, mitigating disease mechanisms. In addition to their roles in AD pathogenesis, EVs also exhibit great potential for the diagnosis and treatment of other brain disorders, representing an advantageous tool for Precision Medicine. Herein, we summarize the contribution of small EVs to AD-related mechanisms and disease progression, as well as their potential as diagnostic and therapeutic agents for AD.

Indexed as

Alzheimer DiseaseExtracellular VesiclesAmyloid beta-PeptidesDisease ProgressionHumansPrecision MedicineAmyloid beta-PeptidesAlzheimer's diseaseDiagnosisExosomesExtracellular vesiclesPrecision medicineProgressionTreatment

Identifiers

PMID35952764
PMCPMC9985072
OpenAlexW4294553463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.