TY - JOUR
T1 - Uncovering a neurological protein signature for severe COVID-19
AU - El-Agnaf, Omar
AU - Bensmail, Ilham
AU - Al-Nesf, Maryam A.Y.
AU - Flynn, James
AU - Taylor, Mark
AU - Majbour, Nour K.
AU - Abdi, Ilham Y.
AU - Vaikath, Nishant N.
AU - Farooq, Abdulaziz
AU - Vemulapalli, Praveen B.
AU - Schmidt, Frank
AU - Ouararhni, Khalid
AU - Al-Siddiqi, Heba H.
AU - Arredouani, Abdelilah
AU - Wijten, Patrick
AU - Al-Maadheed, Mohammed
AU - Mohamed-Ali, Vidya
AU - Decock, Julie
AU - Abdesselem, Houari B.
N1 - Publisher Copyright:
© 2023 The Author(s)
PY - 2023/6/15
Y1 - 2023/6/15
N2 - Coronavirus disease of 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has sparked a global pandemic with severe complications and high morbidity rate. Neurological symptoms in COVID-19 patients, and neurological sequelae post COVID-19 recovery have been extensively reported. Yet, neurological molecular signature and signaling pathways that are affected in the central nervous system (CNS) of COVID-19 severe patients remain still unknown and need to be identified. Plasma samples from 49 severe COVID-19 patients, 50 mild COVID-19 patients, and 40 healthy controls were subjected to Olink proteomics analysis of 184 CNS-enriched proteins. By using a multi-approach bioinformatics analysis, we identified a 34-neurological protein signature for COVID-19 severity and unveiled dysregulated neurological pathways in severe cases. Here, we identified a new neurological protein signature for severe COVID-19 that was validated in different independent cohorts using blood and postmortem brain samples and shown to correlate with neurological diseases and pharmacological drugs. This protein signature could potentially aid the development of prognostic and diagnostic tools for neurological complications in post-COVID-19 convalescent patients with long term neurological sequelae.
AB - Coronavirus disease of 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has sparked a global pandemic with severe complications and high morbidity rate. Neurological symptoms in COVID-19 patients, and neurological sequelae post COVID-19 recovery have been extensively reported. Yet, neurological molecular signature and signaling pathways that are affected in the central nervous system (CNS) of COVID-19 severe patients remain still unknown and need to be identified. Plasma samples from 49 severe COVID-19 patients, 50 mild COVID-19 patients, and 40 healthy controls were subjected to Olink proteomics analysis of 184 CNS-enriched proteins. By using a multi-approach bioinformatics analysis, we identified a 34-neurological protein signature for COVID-19 severity and unveiled dysregulated neurological pathways in severe cases. Here, we identified a new neurological protein signature for severe COVID-19 that was validated in different independent cohorts using blood and postmortem brain samples and shown to correlate with neurological diseases and pharmacological drugs. This protein signature could potentially aid the development of prognostic and diagnostic tools for neurological complications in post-COVID-19 convalescent patients with long term neurological sequelae.
KW - Neurological complications
KW - Olink proteomics
KW - Protein signature
KW - Severe COVID-19
UR - http://www.scopus.com/inward/record.url?scp=85159206190&partnerID=8YFLogxK
U2 - 10.1016/j.nbd.2023.106147
DO - 10.1016/j.nbd.2023.106147
M3 - Article
C2 - 37178811
AN - SCOPUS:85159206190
SN - 0969-9961
VL - 182
JO - Neurobiology of Disease
JF - Neurobiology of Disease
M1 - 106147
ER -