» Articles » PMID: 39086962

Whole Patient Knowledge Modeling of COVID-19 Symptomatology Reveals Common Molecular Mechanisms

Overview
Journal Front Mol Med
Date 2024 Aug 1
PMID 39086962
Authors
Affiliations
Soon will be listed here.
Abstract

Infection with SARS-CoV-2 coronavirus causes systemic, multi-faceted COVID-19 disease. However, knowledge connecting its intricate clinical manifestations with molecular mechanisms remains fragmented. Deciphering the molecular basis of COVID-19 at the whole-patient level is paramount to the development of effective therapeutic approaches. With this goal in mind, we followed an iterative, expert-driven process to compile data published prior to and during the early stages of the pandemic into a comprehensive COVID-19 knowledge model. Recent updates to this model have also validated multiple earlier predictions, suggesting the importance of such knowledge frameworks in hypothesis generation and testing. Overall, our findings suggest that SARS-CoV-2 perturbs several specific mechanisms, unleashing a pathogenesis spectrum, ranging from "a perfect storm" triggered by acute hyper-inflammation, to accelerated aging in protracted "long COVID-19" syndromes. In this work, we shortly report on these findings that we share with the community 1) a synopsis of key evidence associating COVID-19 symptoms and plausible mechanisms, with details presented within 2) the accompanying "COVID-19 Explorer" webserver, developed specifically for this purpose (found at https://covid19.molecularhealth.com). We anticipate that our model will continue to facilitate clinico-molecular insights across organ systems together with hypothesis generation for the testing of potential repurposing drug candidates, new pharmacological targets and clinically relevant biomarkers. Our work suggests that whole patient knowledge models of human disease can potentially expedite the development of new therapeutic strategies and support evidence-driven clinical hypothesis generation and decision making.

Citing Articles

A brief reference to AI-driven audible reality (AuRa) in open world: potential, applications, and evaluation.

Ates O, Pandey G, Gousiopoulos A, Soldatos T Front Artif Intell. 2024; 7:1424371.

PMID: 39525498 PMC: 11543578. DOI: 10.3389/frai.2024.1424371.


Rewiring Drug Research and Development through Human Data-Driven Discovery (HD).

Jackson D, Racz R, Kim S, Brock S, Burkhart K Pharmaceutics. 2023; 15(6).

PMID: 37376121 PMC: 10303279. DOI: 10.3390/pharmaceutics15061673.

References
1.
Tukiainen T, Villani A, Yen A, Rivas M, Marshall J, Satija R . Landscape of X chromosome inactivation across human tissues. Nature. 2017; 550(7675):244-248. PMC: 5685192. DOI: 10.1038/nature24265. View

2.
Kellner M, Noonepalle S, Lu Q, Srivastava A, Zemskov E, Black S . ROS Signaling in the Pathogenesis of Acute Lung Injury (ALI) and Acute Respiratory Distress Syndrome (ARDS). Adv Exp Med Biol. 2017; 967:105-137. PMC: 7120947. DOI: 10.1007/978-3-319-63245-2_8. View

3.
Waldman M, Cohen K, Yadin D, Nudelman V, Gorfil D, Laniado-Schwartzman M . Regulation of diabetic cardiomyopathy by caloric restriction is mediated by intracellular signaling pathways involving 'SIRT1 and PGC-1α'. Cardiovasc Diabetol. 2018; 17(1):111. PMC: 6090985. DOI: 10.1186/s12933-018-0754-4. View

4.
Brilha S, Ong C, Weksler B, Romero N, Couraud P, Friedland J . Matrix metalloproteinase-9 activity and a downregulated Hedgehog pathway impair blood-brain barrier function in an in vitro model of CNS tuberculosis. Sci Rep. 2017; 7(1):16031. PMC: 5700087. DOI: 10.1038/s41598-017-16250-3. View

5.
Tharaux P, Dhaun N . Endothelium-Neutrophil Communication B1-Kinin Receptor-Bearing Microvesicles in Vasculitis. J Am Soc Nephrol. 2017; 28(8):2255-2258. PMC: 5533246. DOI: 10.1681/ASN.2017030300. View