Evidence map›Paper›PMID 37873207›Full record

ArticlebioRxiv : the preprint server for biology2023

Assessment of brain-derived extracellular vesicle enrichment for blood biomarker analysis in age-related neurodegenerative diseases: An international overview.

AmanPreet Badhwar, Yael Hirschberg, Natalia Valle Tamayo, M Florencia Iulita, Chinedu T Udeh-Momoh, Anna Matton, Rawan M Tarawneh, Robert A Rissman, Aurélie Ledreux, Charisse N Winston and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 7 countries.

AmanPreet BadhwarORCID 0000-0003-3414-3395
Natalia Valle Tamayo
M Florencia IulitaORCID 0000-0002-3360-4498
Chinedu T Udeh-MomohORCID 0000-0002-7357-4692
Charisse N WinstonORCID 0000-0002-1966-9252
Arsalan S HaqqaniORCID 0000-0003-2454-8989
Alzheimer’s Association International Society to Advance Alzheimer's Research and Treatment, BBB-EWG
Hospital de Sant Pau · ESKarolinska University Hospital · SEUniversity of Southern California · USInstitut Universitaire de Gériatrie de Montréal · CANational Research Council Canada · CAUniversity of Antwerp · BEUniversity of Colorado Anschutz Medical Campus · USUniversity of New Mexico · US

Funding

USCADRC Diversity Supplement PachicanoP30AG066530 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HELENA Chang CHUI, ARTHUR W TOGA · 2020 to 2026
$27.8M
Elucidating the Role of Endothelial Dysfunction in Alzheimer Disease: Towards A New Data-Driven Disease ModelRF1AG083744 · NIA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI TARAWNEH, RAWAN · 2023 to 2023
$2.1M
UCSD Leading the Advancement of Underrepresented Neuroscientists for Change (LAUNCH) Faculty Development ProgramR25NS117367 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Victoria B Risbrough, Joann Trejo · 2020 to 2026
$1.6M
NIA NIH HHS P30 AG066530NIA NIH HHS RF1 AG083744NINDS NIH HHS R25 NS117367
6 · The paper itself

Abstract

introductionBrain-derived extracellular vesicles (BEVs) in blood allows for minimally- invasive investigations of CNS-specific markers of age-related neurodegenerative diseases (NDDs). Polymer-based EV- and immunoprecipitation (IP)-based BEV-enrichment protocols from blood have gained popularity. We systematically investigated protocol consistency across studies, and determined CNS-specificity of proteins associated with these protocols.

methodsNDD articles investigating BEVs in blood using polymer-based and/or IP-based BEV enrichment protocols were systematically identified, and protocols compared. Proteins used for BEV-enrichment and/or post-enrichment were assessed for CNS- and brain-cell-type- specificity; extracellular domains (ECD+); and presence in EV-databases.

results82.1% of studies used polymer-based (ExoQuick) EV-enrichment, and 92.3% used L1CAM for IP-based BEV-enrichment. Centrifugation times differed across studies. 26.8% of 82 proteins systematically identified were CNS-specific: 50% ECD+, 77.3% were listed in EV- databases. DISCUSSION: We identified protocol steps requiring standardization, and recommend additional CNS-specific proteins that can be used for BEV-enrichment or as BEV-biomarkers.

Identifiers

PMID37873207
PMCPMC10592861
OpenAlexW4387307980

What OpenQuestion holds

Textmetadata
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.