TY - JOUR
T1 - The Adverse Outcome Pathway Framework Applied to Neurological Symptoms of COVID-19
AU - Hogberg, Helena T.
AU - Lam, Ann
AU - Ohayon, Elan
AU - Shahbaz, Muhammad Ali
AU - Clerbaux, Laure Alix
AU - Bal-Price, Anna
AU - Coecke, Sandra
AU - Concha, Rachel
AU - De Bernardi, Francesca
AU - Edrosa, Eizleayne
AU - Hargreaves, Alan J.
AU - Kanninen, Katja M.
AU - Munoz, Amalia
AU - Pistollato, Francesca
AU - Saravanan, Surat
AU - Garcia-Reyero, Natàlia
AU - Wittwehr, Clemens
AU - Sachana, Magdalini
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/11
Y1 - 2022/11
N2 - 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.
AB - 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.
KW - AOP
KW - SARS-CoV-2
KW - anosmia
KW - encephalitis
KW - human-specific research
KW - neuropathology
KW - stroke
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U2 - 10.3390/cells11213411
DO - 10.3390/cells11213411
M3 - Review article
C2 - 36359807
AN - SCOPUS:85141566744
SN - 2073-4409
VL - 11
JO - Cells
JF - Cells
IS - 21
M1 - 3411
ER -