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Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients

The Coronavirus Disease 2019 (COVID-19) has affected all aspects of life around the world. Neuroimaging evidence suggests the novel coronavirus can attack the central nervous system (CNS), causing cerebro-vascular abnormalities in the brain. This can lead to focal changes in cerebral blood flow and...

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Autores principales: Hafiz, Rakibul, Gandhi, Tapan Kumar, Mishra, Sapna, Prasad, Alok, Mahajan, Vidur, Natelson, Benjamin H., Di, Xin, Biswal, Bharat B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820653/
https://www.ncbi.nlm.nih.gov/pubmed/35132408
http://dx.doi.org/10.1101/2022.02.01.478677
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author Hafiz, Rakibul
Gandhi, Tapan Kumar
Mishra, Sapna
Prasad, Alok
Mahajan, Vidur
Natelson, Benjamin H.
Di, Xin
Biswal, Bharat B.
author_facet Hafiz, Rakibul
Gandhi, Tapan Kumar
Mishra, Sapna
Prasad, Alok
Mahajan, Vidur
Natelson, Benjamin H.
Di, Xin
Biswal, Bharat B.
author_sort Hafiz, Rakibul
collection PubMed
description The Coronavirus Disease 2019 (COVID-19) has affected all aspects of life around the world. Neuroimaging evidence suggests the novel coronavirus can attack the central nervous system (CNS), causing cerebro-vascular abnormalities in the brain. This can lead to focal changes in cerebral blood flow and metabolic oxygen consumption rate in the brain. However, the extent and spatial locations of brain alterations in COVID-19 survivors are largely unknown. In this study, we have assessed brain functional connectivity (FC) using resting-state functional MRI (RS-fMRI) in 38 (25 males) COVID patients two weeks after hospital discharge, when PCR negative and 31 (24 males) healthy subjects. FC was estimated using independent component analysis (ICA) and dual regression. When compared to the healthy group, the COVID group demonstrated significantly enhanced FC in the basal ganglia and precuneus networks (family wise error (fwe) corrected, p(fwe) < 0.05), while, on the other hand, reduced FC in the language network (p(fwe) < 0.05). The COVID group also experienced higher fatigue levels during work, compared to the healthy group (p < 0.001). Moreover, within the precuneus network, we noticed a significant negative correlation between FC and fatigue scores across groups (Spearman’s ρ = −0.47, p = 0.001, r(2) = 0.22). Interestingly, this relationship was found to be significantly stronger among COVID survivors within the left parietal lobe, which is known to be structurally and functionally associated with fatigue in other neurological disorders.
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spelling pubmed-88206532022-02-08 Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients Hafiz, Rakibul Gandhi, Tapan Kumar Mishra, Sapna Prasad, Alok Mahajan, Vidur Natelson, Benjamin H. Di, Xin Biswal, Bharat B. bioRxiv Article The Coronavirus Disease 2019 (COVID-19) has affected all aspects of life around the world. Neuroimaging evidence suggests the novel coronavirus can attack the central nervous system (CNS), causing cerebro-vascular abnormalities in the brain. This can lead to focal changes in cerebral blood flow and metabolic oxygen consumption rate in the brain. However, the extent and spatial locations of brain alterations in COVID-19 survivors are largely unknown. In this study, we have assessed brain functional connectivity (FC) using resting-state functional MRI (RS-fMRI) in 38 (25 males) COVID patients two weeks after hospital discharge, when PCR negative and 31 (24 males) healthy subjects. FC was estimated using independent component analysis (ICA) and dual regression. When compared to the healthy group, the COVID group demonstrated significantly enhanced FC in the basal ganglia and precuneus networks (family wise error (fwe) corrected, p(fwe) < 0.05), while, on the other hand, reduced FC in the language network (p(fwe) < 0.05). The COVID group also experienced higher fatigue levels during work, compared to the healthy group (p < 0.001). Moreover, within the precuneus network, we noticed a significant negative correlation between FC and fatigue scores across groups (Spearman’s ρ = −0.47, p = 0.001, r(2) = 0.22). Interestingly, this relationship was found to be significantly stronger among COVID survivors within the left parietal lobe, which is known to be structurally and functionally associated with fatigue in other neurological disorders. Cold Spring Harbor Laboratory 2023-01-28 /pmc/articles/PMC8820653/ /pubmed/35132408 http://dx.doi.org/10.1101/2022.02.01.478677 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Hafiz, Rakibul
Gandhi, Tapan Kumar
Mishra, Sapna
Prasad, Alok
Mahajan, Vidur
Natelson, Benjamin H.
Di, Xin
Biswal, Bharat B.
Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title_full Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title_fullStr Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title_full_unstemmed Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title_short Assessing functional connectivity differences and work-related fatigue in surviving COVID-negative patients
title_sort assessing functional connectivity differences and work-related fatigue in surviving covid-negative patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820653/
https://www.ncbi.nlm.nih.gov/pubmed/35132408
http://dx.doi.org/10.1101/2022.02.01.478677
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