Evidence map›Paper›PMID 35484240›Full record

ArticleMolecular psychiatry2024

Apolipoprotein E potently inhibits ferroptosis by blocking ferritinophagy.

Abdel Ali Belaidi, Shashank Masaldan, Adam Southon, Pawel Kalinowski, Karla Acevedo, Ambili T Appukuttan, Stuart Portbury, Peng Lei, Puja Agarwal, Sue E Leurgans and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
14.6field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Review
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  9. Review
  10. Autophagy regulation of pyroptosis and ferroptosis: a new strategy for colorectal cancer treatment.Apoptosis : an international journal on programmed cell death · 2026
    Review
  11. Review
  12. Review
  13. Review
  14. Autophagy-lysosomal pathway in neurodegeneration.Molecular neurodegeneration advances · 2026
    Review
  15. Article
  16. Aberrant Mitochondrial Metabolism in Alzheimer's Disease Links Energy Stress with Ferroptosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  17. Neuroferroptosis in health and diseases.Nature reviews. Neuroscience · 2025
    Review
  18. Article
  19. Article
  20. Article
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

14 authors at 4 institutions in 5 countries.

Abdel Ali BelaidiMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.ORCID 0000-0003-0792-8728
Shashank MasaldanMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.ORCID 0000-0003-4960-4983
Adam SouthonMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
Pawel KalinowskiMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
Karla AcevedoMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
Ambili T AppukuttanMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
Stuart PortburyMelbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
Peng LeiDepartment of Neurology and State Key Laboratory of Biotherapy, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.ORCID 0000-0001-5652-1962
Puja AgarwalRush Alzheimer Disease Center, Rush University Medical Center, Chicago, United States.ORCID 0000-0002-0274-6653
Sue E LeurgansRush Alzheimer Disease Center, Rush University Medical Center, Chicago, United States.ORCID 0000-0003-2536-1665
Julie SchneiderRush Alzheimer Disease Center, Rush University Medical Center, Chicago, United States.
Marcus ConradHelmholtz Zentrum München, Institute of Metabolism and Cell Death, 85764, Neuherberg, Germany.ORCID 0000-0003-1140-5612
Ashley I Bush *Melbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia. ashley.bush@florey.edu.au.ORCID 0000-0001-8259-9069
Scott Ayton *Melbourne Dementia Research Centre, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia. scott.ayton@florey.edu.au.ORCID 0000-0002-3479-2427
The University of Melbourne · AURush University Medical Center · USHelmholtz Zentrum München · DESichuan University · CN

Funding

EPIDEMIOLOGY OF NEURAL RESERVE AND NEUROBIOLOGY IN AGINGR01AG017917 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI BENNETT, DAVID ALAN · 2001 to 2023
$43.3M
Neuropathologic-Epidemiological Study of Metallomics and Alzheimer's DiseaseR01AG054057 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI Julie A. Schneider · 2022 to 2026
$3.0M
Neuropathologic-Epidemiological Study of Metallomics and Alzheimer's DiseaseRF1AG054057 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI BUSH, ASHLEY I, SCHNEIDER, JULIE A. · 2016 to 2016
$2.8M
Alzheimer's Association AARFD-16-442821NIA NIH HHS R01 AG017917NIA NIH HHS R01 AG054057NIA NIH HHS RF1 AG054057
6 · The paper itself

Abstract

Allelic variation to the APOE gene confers the greatest genetic risk for sporadic Alzheimer's disease (AD). Independent of genotype, low abundance of apolipoprotein E (apoE), is characteristic of AD CSF, and predicts cognitive decline. The mechanisms underlying the genotype and apoE level risks are uncertain. Recent fluid and imaging biomarker studies have revealed an unexpected link between apoE and brain iron, which also forecasts disease progression, possibly through ferroptosis, an iron-dependent regulated cell death pathway. Here, we report that apoE is a potent inhibitor of ferroptosis (EC

Indexed as

Alzheimer DiseaseApolipoproteins EAutophagyFerritinsFerroptosisIronAgedAged, 80 and overAllelesAnimalsApolipoprotein E4BrainFemaleGenotypeHumansLipid PeroxidationApolipoprotein E4Apolipoproteins EFerritinsIron

Identifiers

PMID35484240
PMCPMC9757994
OpenAlexW4224980565

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.