Evidence map›Paper›PMID 36269539›Full record

ReviewCurrent neurology and neuroscience reports2022

Vascular Considerations for Amyloid Immunotherapy.

Kate E Foley, Donna M Wilcock

Open access · greenAbstract readReview
In one paragraph

Review in Current neurology and neuroscience reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. WSB.bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. The striatum is an early, accurate indicator of amyloid burden using [Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. 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

2 authors at 1 institution in 1 country.

Kate E FoleySanders-Brown Center On Aging, Department of Physiology, University of Kentucky, Lexington, KY, USA.ORCID 0000-0001-5110-238X
Donna M WilcockSanders-Brown Center On Aging, Department of Physiology, University of Kentucky, Lexington, KY, USA. donna.wilcock@uky.edu.ORCID 0000-0003-3388-1564
University of Kentucky · US

Funding

University of Kentucky Alzheimer's Disease Research CenterP30AG072946 · NIA · UNIVERSITY OF KENTUCKY · PI LINDA J VAN ELDIK · 2021 to 2026
$23.5M
Training in Translational Research in Alzheimer's and Related Dementias (TRIAD)T32AG078110 · NIA · UNIVERSITY OF KENTUCKY · PI Michael Paul Murphy, LINDA J VAN ELDIK · 2022 to 2026
$2.3M
Training in Translational Research in Alzheimer's and Related Dementias (TRIAD)T32AG057461 · NIA · UNIVERSITY OF KENTUCKY · PI MURPHY, MICHAEL PAUL, VAN ELDIK, LINDA J · 2017 to 2021
$2.1M
Establishing the role of MMP9 in amyloid-immunotherapy-induced ARIARF1NS130834 · NINDS · UNIVERSITY OF KENTUCKY · PI WILCOCK, DONNA M · 2022 to 2022
$1.7M
Establishing the role of MMP9 in amyloid-immunotherapy-induced ARIAR01NS130834 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI Donna M Wilcock · 2025 to 2026
$989k
NIA NIH HHS P30 AG072946NIA NIH HHS T32 AG057461NIA NIH HHS T32 AG078110NINDS NIH HHS R01 NS130834NINDS NIH HHS RF1 NS130834
6 · The paper itself

Abstract

purpose of reviewAmyloid beta (Aβ) plaque accumulation is a hallmark pathology contributing to Alzheimer's disease (AD) and is widely hypothesized to lead to cognitive decline. Decades of research into anti-Aβ immunotherapies provide evidence for increased Aβ clearance from the brain; however, this is frequently accompanied by complicated vascular deficits. This article reviews the history of anti-Aβ immunotherapies and clinical findings and provides recommendations moving forward. RECENT

findingsIn 20 years of both animal and human studies, anti-Aβ immunotherapies have been a prevalent avenue of reducing hallmark Aβ plaques. In both models and with different anti-Aβ antibody designs, amyloid-related imaging abnormalities (ARIA) indicating severe cerebrovascular compromise have been common and concerning occurrence. ARIA caused by anti-Aβ immunotherapy has been noted since the early 2000s, and the mechanisms driving it are still unknown. Recent approval of aducanumab comes with renewed urgency to consider vascular deficits caused by anti-Aβ immunotherapy.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloidAmyloidogenic ProteinsAnimalsDisease Models, AnimalHumansImmunologic FactorsImmunotherapyPlaque, AmyloidAmyloidAmyloid beta-PeptidesAmyloidogenic ProteinsImmunologic FactorsAducanumabAlzheimer’s diseaseAmyloidBiomarkersImmunotherapyVascular

Identifiers

PMID36269539
PMCPMC9714255
OpenAlexW4306986465

What OpenQuestion holds

Textmetadata
LicenceTDM
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.