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Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms

IMPORTANCE: Persistent depressive symptoms, often accompanied by cognitive symptoms, commonly occur after COVID-19 illness (hereinafter termed COVID-DC, DC for depressive and/or cognitive symptoms). In patients with COVID-DC, gliosis, an inflammatory change, was suspected, but measurements of gliosi...

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Autores principales: Braga, Joeffre, Lepra, Mariel, Kish, Stephen J., Rusjan, Pablo. M., Nasser, Zahra, Verhoeff, Natasha, Vasdev, Neil, Bagby, Michael, Boileau, Isabelle, Husain, M. Ishrat, Kolla, Nathan, Garcia, Armando, Chao, Thomas, Mizrahi, Romina, Faiz, Khunsa, Vieira, Erica L., Meyer, Jeffrey H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233457/
https://www.ncbi.nlm.nih.gov/pubmed/37256580
http://dx.doi.org/10.1001/jamapsychiatry.2023.1321
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author Braga, Joeffre
Lepra, Mariel
Kish, Stephen J.
Rusjan, Pablo. M.
Nasser, Zahra
Verhoeff, Natasha
Vasdev, Neil
Bagby, Michael
Boileau, Isabelle
Husain, M. Ishrat
Kolla, Nathan
Garcia, Armando
Chao, Thomas
Mizrahi, Romina
Faiz, Khunsa
Vieira, Erica L.
Meyer, Jeffrey H.
author_facet Braga, Joeffre
Lepra, Mariel
Kish, Stephen J.
Rusjan, Pablo. M.
Nasser, Zahra
Verhoeff, Natasha
Vasdev, Neil
Bagby, Michael
Boileau, Isabelle
Husain, M. Ishrat
Kolla, Nathan
Garcia, Armando
Chao, Thomas
Mizrahi, Romina
Faiz, Khunsa
Vieira, Erica L.
Meyer, Jeffrey H.
author_sort Braga, Joeffre
collection PubMed
description IMPORTANCE: Persistent depressive symptoms, often accompanied by cognitive symptoms, commonly occur after COVID-19 illness (hereinafter termed COVID-DC, DC for depressive and/or cognitive symptoms). In patients with COVID-DC, gliosis, an inflammatory change, was suspected, but measurements of gliosis had not been studied in the brain for this condition. OBJECTIVE: To determine whether translocator protein total distribution volume (TSPO V(T)), a marker of gliosis that is quantifiable with positron emission tomography (PET), is elevated in the dorsal putamen, ventral striatum, prefrontal cortex, anterior cingulate cortex, and hippocampus of persons with COVID-DC. DESIGN, SETTING, AND PARTICIPANTS: This case-control study conducted at a tertiary care psychiatric hospital in Canada from April 1, 2021, to June 30, 2022, compared TSPO V(T) of specific brain regions in 20 participants with COVID-DC with that in 20 healthy controls. The TSPO V(T) was measured with fluorine F 18–labeled N-(2-(2-fluoroethoxy)benzyl)-N-(4-phenoxypyridin-3-yl)acetamide ([(18)F]FEPPA) PET. MAIN OUTCOMES AND MEASURES: The TSPO V(T) was measured in the dorsal putamen, ventral striatum, prefrontal cortex, anterior cingulate cortex, and hippocampus. Symptoms were measured with neuropsychological and psychological tests, prioritizing outcomes related to striatal function. RESULTS: The study population included 40 participants (mean [SD] age, 32.9 [12.3] years). The TSPO V(T) across the regions of interest was greater in persons with COVID-DC (mean [SD] age, 32.7 [11.4] years; 12 [60%] women) compared with healthy control participants (mean [SD] age, 33.3 [13.9] years; 11 [55%] women): mean (SD) difference, 1.51 (4.47); 95% CI, 0.04-2.98; 1.51 divided by 9.20 (17%). The difference was most prominent in the ventral striatum (mean [SD] difference, 1.97 [4.88]; 95% CI, 0.36-3.58; 1.97 divided by 8.87 [22%]) and dorsal putamen (mean difference, 1.70 [4.25]; 95% CI, 0.34-3.06; 1.70 divided by 8.37 [20%]). Motor speed on the finger-tapping test negatively correlated with dorsal putamen TSPO V(T) (r, −0.53; 95% CI, −0.79 to −0.09), and the 10 persons with the slowest speed among those with COVID-DC had higher dorsal putamen TSPO V(T) than healthy persons by 2.3 (2.30 divided by 8.37 [27%]; SD, 2.46; 95% CI, 0.92-3.68). CONCLUSIONS AND RELEVANCE: In this case-control study, TSPO V(T) was higher in patients with COVID-DC. Greater TSPO V(T) is evidence for an inflammatory change of elevated gliosis in the brain of an individual with COVID-DC. Gliosis may be consequent to inflammation, injury, or both, particularly in the ventral striatum and dorsal putamen, which may explain some persistent depressive and cognitive symptoms, including slowed motor speed, low motivation or energy, and anhedonia, after initially mild to moderate COVID-19 illness.
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spelling pubmed-102334572023-06-02 Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms Braga, Joeffre Lepra, Mariel Kish, Stephen J. Rusjan, Pablo. M. Nasser, Zahra Verhoeff, Natasha Vasdev, Neil Bagby, Michael Boileau, Isabelle Husain, M. Ishrat Kolla, Nathan Garcia, Armando Chao, Thomas Mizrahi, Romina Faiz, Khunsa Vieira, Erica L. Meyer, Jeffrey H. JAMA Psychiatry Original Investigation IMPORTANCE: Persistent depressive symptoms, often accompanied by cognitive symptoms, commonly occur after COVID-19 illness (hereinafter termed COVID-DC, DC for depressive and/or cognitive symptoms). In patients with COVID-DC, gliosis, an inflammatory change, was suspected, but measurements of gliosis had not been studied in the brain for this condition. OBJECTIVE: To determine whether translocator protein total distribution volume (TSPO V(T)), a marker of gliosis that is quantifiable with positron emission tomography (PET), is elevated in the dorsal putamen, ventral striatum, prefrontal cortex, anterior cingulate cortex, and hippocampus of persons with COVID-DC. DESIGN, SETTING, AND PARTICIPANTS: This case-control study conducted at a tertiary care psychiatric hospital in Canada from April 1, 2021, to June 30, 2022, compared TSPO V(T) of specific brain regions in 20 participants with COVID-DC with that in 20 healthy controls. The TSPO V(T) was measured with fluorine F 18–labeled N-(2-(2-fluoroethoxy)benzyl)-N-(4-phenoxypyridin-3-yl)acetamide ([(18)F]FEPPA) PET. MAIN OUTCOMES AND MEASURES: The TSPO V(T) was measured in the dorsal putamen, ventral striatum, prefrontal cortex, anterior cingulate cortex, and hippocampus. Symptoms were measured with neuropsychological and psychological tests, prioritizing outcomes related to striatal function. RESULTS: The study population included 40 participants (mean [SD] age, 32.9 [12.3] years). The TSPO V(T) across the regions of interest was greater in persons with COVID-DC (mean [SD] age, 32.7 [11.4] years; 12 [60%] women) compared with healthy control participants (mean [SD] age, 33.3 [13.9] years; 11 [55%] women): mean (SD) difference, 1.51 (4.47); 95% CI, 0.04-2.98; 1.51 divided by 9.20 (17%). The difference was most prominent in the ventral striatum (mean [SD] difference, 1.97 [4.88]; 95% CI, 0.36-3.58; 1.97 divided by 8.87 [22%]) and dorsal putamen (mean difference, 1.70 [4.25]; 95% CI, 0.34-3.06; 1.70 divided by 8.37 [20%]). Motor speed on the finger-tapping test negatively correlated with dorsal putamen TSPO V(T) (r, −0.53; 95% CI, −0.79 to −0.09), and the 10 persons with the slowest speed among those with COVID-DC had higher dorsal putamen TSPO V(T) than healthy persons by 2.3 (2.30 divided by 8.37 [27%]; SD, 2.46; 95% CI, 0.92-3.68). CONCLUSIONS AND RELEVANCE: In this case-control study, TSPO V(T) was higher in patients with COVID-DC. Greater TSPO V(T) is evidence for an inflammatory change of elevated gliosis in the brain of an individual with COVID-DC. Gliosis may be consequent to inflammation, injury, or both, particularly in the ventral striatum and dorsal putamen, which may explain some persistent depressive and cognitive symptoms, including slowed motor speed, low motivation or energy, and anhedonia, after initially mild to moderate COVID-19 illness. American Medical Association 2023-05-31 2023-08 /pmc/articles/PMC10233457/ /pubmed/37256580 http://dx.doi.org/10.1001/jamapsychiatry.2023.1321 Text en Copyright 2023 Braga J et al. JAMA Psychiatry. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Braga, Joeffre
Lepra, Mariel
Kish, Stephen J.
Rusjan, Pablo. M.
Nasser, Zahra
Verhoeff, Natasha
Vasdev, Neil
Bagby, Michael
Boileau, Isabelle
Husain, M. Ishrat
Kolla, Nathan
Garcia, Armando
Chao, Thomas
Mizrahi, Romina
Faiz, Khunsa
Vieira, Erica L.
Meyer, Jeffrey H.
Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title_full Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title_fullStr Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title_full_unstemmed Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title_short Neuroinflammation After COVID-19 With Persistent Depressive and Cognitive Symptoms
title_sort neuroinflammation after covid-19 with persistent depressive and cognitive symptoms
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233457/
https://www.ncbi.nlm.nih.gov/pubmed/37256580
http://dx.doi.org/10.1001/jamapsychiatry.2023.1321
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