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Neurological sequelae of long COVID: a comprehensive review of diagnostic imaging, underlying mechanisms, and potential therapeutics

Talkington et al., Frontiers in Neurology, doi:10.3389/fneur.2024.1465787, Feb 2025
https://c19early.org/talkington.html
Review of neurological sequelae of long COVID (LC), focusing on cognitive dysfunction, diagnostic tools, underlying mechanisms, and potential therapeutic approaches. The authors examine how long COVID can cause chronic insomnia, fatigue, mood disorders, and cognitive impairments. Several mechanistic hypotheses are explored, including CNS invasion, neuroinflammation, blood-brain barrier disruption, gut-brain axis dysregulation, and vascular disruption.
Talkington et al., 7 Feb 2025, peer-reviewed, 19 authors. Contact: gbix@tulane.edu.
Neurological sequelae of long COVID: a comprehensive review of diagnostic imaging, underlying mechanisms, and potential therapeutics
Caleb Mcentire, Antonio Osmar, Jaramillo-Morales, Gregory J Bix, Grant Mcgee Talkington, Paresh Kolluru, Timothy E Gressett, Saifudeen Ismael, Umar Meenakshi, Mariana Acquarone, Rebecca J Solch-Ottaiano, Amanda White, Blake Ouvrier, Kristina Par, Nicholas Parker, Amanda Watters, Nabeela Siddeeque, Brooke Sullivan, Nilesh Ganguli, Victor Calero-Hernandez, Gregory Hall, Michele Longo
One lingering e ect of the COVID-pandemic created by SARS-CoV-is the emergence of Long COVID (LC), characterized by enduring neurological sequelae a ecting a significant portion of survivors. This review provides a thorough analysis of these neurological disruptions with respect to cognitive dysfunction, which broadly manifest as chronic insomnia, fatigue, mood dysregulation, and cognitive impairments with respect to cognitive dysfunction. Furthermore, we characterize how diagnostic tools such as PET, MRI, EEG, and ultrasonography provide critical insight into subtle neurological anomalies that may mechanistically explain the Long COVID disease phenotype. In this review, we explore the mechanistic hypotheses of these neurological changes, which describe CNS invasion, neuroinflammation, blood-brain barrier disruption, and gut-brain axis dysregulation, along with the novel vascular disruption hypothesis that highlights endothelial dysfunction and hypoperfusion as a core underlying mechanism. We lastly evaluate the clinical treatment landscape, scrutinizing the e cacy of various therapeutic strategies ranging from antivirals to antiinflammatory agents in mitigating the multifaceted symptoms of LC.
Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision. Publisher's note All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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In this review, we explore the mechanistic hypotheses of these neurological changes, which describe CNS invasion, neuroinflammation, blood-brain barrier disruption, and gut-brain axis dysregulation, along with the novel vascular disruption hypothesis that highlights endothelial dysfunction and hypoperfusion as a core underlying mechanism. 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