Evidence map›Paper›PMID 36359807›Full record

ReviewCells2022

The Adverse Outcome Pathway Framework Applied to Neurological Symptoms of COVID-19.

Helena T Hogberg, Ann Lam, Elan Ohayon, Muhammad Ali Shahbaz, Laure-Alix Clerbaux, Anna Bal-Price, Sandra Coecke, Rachel Concha, Francesca De Bernardi, Eizleayne Edrosa and 8 more

Abstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

18 authors.

Helena T HogbergNational Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27518, USA.
Ann LamGreen Neuroscience Laboratory, Neurolinx Research Institute, San Diego, CA 92111, USA.
Elan OhayonGreen Neuroscience Laboratory, Neurolinx Research Institute, San Diego, CA 92111, USA.
Muhammad Ali ShahbazA.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0002-7193-6792
Laure-Alix ClerbauxEuropean Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.ORCID 0000-0003-2707-482X
Anna Bal-PriceEuropean Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.
Sandra CoeckeEuropean Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.ORCID 0000-0003-2773-6408
Rachel ConchaGreen Neuroscience Laboratory, Neurolinx Research Institute, San Diego, CA 92111, USA.
Francesca De BernardiDivision of Otorhinolaryngology, Department of Biotechnologies and Life Sciences, University of Insubria, Ospedale di Circolo e Fondazione Macchi, 21100 Varese, Italy.
Eizleayne EdrosaGreen Neuroscience Laboratory, Neurolinx Research Institute, San Diego, CA 92111, USA.
Alan J HargreavesSchool of Science and Technology, Nottingham Trent University, Nottingham NG11 8NS, UK.
Katja M KanninenA.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, 70211 Kuopio, Finland.ORCID 0000-0002-6717-8589
Amalia MunozEuropean Commission, Joint Research Centre (JRC), 2440 Geel, Belgium.
Francesca PistollatoEuropean Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.
Surat SaravananCentre for Predictive Human Model Systems Atal Incubation Centre-Centre for Cellular and Molecular Biology, Hyderabad 500039, India.
Natàlia Garcia-ReyeroEnvironmental Laboratory, US Army Engineer Research & Development Center, Vicksburg, MS 39180, USA.ORCID 0000-0002-1667-5294
Clemens WittwehrEuropean Commission, Joint Research Centre (JRC), 21027 Ispra, Italy.
Magdalini SachanaEnvironment Health and Safety Division, Environment Directorate, Organisation for Economic Cooperation and Development (OECD), 75016 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several reports have shown that the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has the potential to also be neurotropic. However, the mechanisms by which SARS-CoV-2 induces neurologic injury, including neurological and/or psychological symptoms, remain unclear. In this review, the available knowledge on the neurobiological mechanisms underlying COVID-19 was organized using the AOP framework. Four AOPs leading to neurological adverse outcomes (AO), anosmia, encephalitis, stroke, and seizure, were developed. Biological key events (KEs) identified to induce these AOs included binding to ACE2, blood-brain barrier (BBB) disruption, hypoxia, neuroinflammation, and oxidative stress. The modularity of AOPs allows the construction of AOP networks to visualize core pathways and recognize neuroinflammation and BBB disruption as shared mechanisms. Furthermore, the impact on the neurological AOPs of COVID-19 by modulating and multiscale factors such as age, psychological stress, nutrition, poverty, and food insecurity was discussed. Organizing the existing knowledge along an AOP framework can represent a valuable tool to understand disease mechanisms and identify data gaps and potentially contribute to treatment, and prevention. This AOP-aligned approach also facilitates synergy between experts from different backgrounds, while the fast-evolving and disruptive nature of COVID-19 emphasizes the need for interdisciplinarity and cross-community research.

Indexed as

Adverse Outcome PathwaysCOVID-19StrokeBlood-Brain BarrierHumansSARS-CoV-2anosmiaAOPencephalitishuman-specific researchneuropathologySARS-CoV-2stroke

Identifiers

PMID36359807
PMCPMC9658029

What OpenQuestion holds

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LicenceCC BY
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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.