Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients

Research output: Contribution to journalJournal articleResearchpeer-review

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Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients. / Miskowiak, Kamilla W.; Bech, Johanne L.; Henriksen, Alexander Cuculiza; Johnsen, Stine; Podlekareva, Daria; Marner, Lisbeth.

In: Brain Sciences, Vol. 13, No. 1, 23, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Miskowiak, KW, Bech, JL, Henriksen, AC, Johnsen, S, Podlekareva, D & Marner, L 2023, 'Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients', Brain Sciences, vol. 13, no. 1, 23. https://doi.org/10.3390/brainsci13010023

APA

Miskowiak, K. W., Bech, J. L., Henriksen, A. C., Johnsen, S., Podlekareva, D., & Marner, L. (2023). Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients. Brain Sciences, 13(1), [23]. https://doi.org/10.3390/brainsci13010023

Vancouver

Miskowiak KW, Bech JL, Henriksen AC, Johnsen S, Podlekareva D, Marner L. Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients. Brain Sciences. 2023;13(1). 23. https://doi.org/10.3390/brainsci13010023

Author

Miskowiak, Kamilla W. ; Bech, Johanne L. ; Henriksen, Alexander Cuculiza ; Johnsen, Stine ; Podlekareva, Daria ; Marner, Lisbeth. / Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients. In: Brain Sciences. 2023 ; Vol. 13, No. 1.

Bibtex

@article{7aa71c26b76a44539f49430c0f2c0d17,
title = "Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients",
abstract = "Background: Common long-term sequelae after COVID-19 include fatigue and cognitive impairment. Although symptoms interfere with daily living, the underlying pathology is largely unknown. Previous studies report relative hypometabolism in frontal, limbic and cerebellar regions suggesting focal brain involvement. We aimed to determine whether absolute hypometabolism was present and correlated to same day standardized neurocognitive testing. Methods: Fourteen patients included from a long COVID clinic had cognitive testing and quantitative dynamic [18F]FDG PET of the brain on the same day to correlate cognitive function to metabolic glucose rate. Results: We found no hypometabolism in frontal, limbic and cerebellar regions in cognitively impaired relative to cognitive intact patients. In contrast, the cognitive impaired patients showed higher cerebellar metabolism (p = 0.03), which correlated with more severe deficits in working memory and executive function (p = 0.03). Conclusions: Hypermetabolism in the cerebellum may reflect inefficient brain processing and play a role in cognitive impairments after COVID-19.",
keywords = "brain fog, brain metabolism, cognitive impairment, COVID-19, FDG, PET, positron emission tomography, quality of life, work function",
author = "Miskowiak, {Kamilla W.} and Bech, {Johanne L.} and Henriksen, {Alexander Cuculiza} and Stine Johnsen and Daria Podlekareva and Lisbeth Marner",
note = "Publisher Copyright: {\textcopyright} 2022 by the authors.",
year = "2023",
doi = "10.3390/brainsci13010023",
language = "English",
volume = "13",
journal = "Brain Sciences",
issn = "2076-3425",
publisher = "M D P I AG",
number = "1",

}

RIS

TY - JOUR

T1 - Cerebral Metabolic Rate of Glucose and Cognitive Tests in Long COVID Patients

AU - Miskowiak, Kamilla W.

AU - Bech, Johanne L.

AU - Henriksen, Alexander Cuculiza

AU - Johnsen, Stine

AU - Podlekareva, Daria

AU - Marner, Lisbeth

N1 - Publisher Copyright: © 2022 by the authors.

PY - 2023

Y1 - 2023

N2 - Background: Common long-term sequelae after COVID-19 include fatigue and cognitive impairment. Although symptoms interfere with daily living, the underlying pathology is largely unknown. Previous studies report relative hypometabolism in frontal, limbic and cerebellar regions suggesting focal brain involvement. We aimed to determine whether absolute hypometabolism was present and correlated to same day standardized neurocognitive testing. Methods: Fourteen patients included from a long COVID clinic had cognitive testing and quantitative dynamic [18F]FDG PET of the brain on the same day to correlate cognitive function to metabolic glucose rate. Results: We found no hypometabolism in frontal, limbic and cerebellar regions in cognitively impaired relative to cognitive intact patients. In contrast, the cognitive impaired patients showed higher cerebellar metabolism (p = 0.03), which correlated with more severe deficits in working memory and executive function (p = 0.03). Conclusions: Hypermetabolism in the cerebellum may reflect inefficient brain processing and play a role in cognitive impairments after COVID-19.

AB - Background: Common long-term sequelae after COVID-19 include fatigue and cognitive impairment. Although symptoms interfere with daily living, the underlying pathology is largely unknown. Previous studies report relative hypometabolism in frontal, limbic and cerebellar regions suggesting focal brain involvement. We aimed to determine whether absolute hypometabolism was present and correlated to same day standardized neurocognitive testing. Methods: Fourteen patients included from a long COVID clinic had cognitive testing and quantitative dynamic [18F]FDG PET of the brain on the same day to correlate cognitive function to metabolic glucose rate. Results: We found no hypometabolism in frontal, limbic and cerebellar regions in cognitively impaired relative to cognitive intact patients. In contrast, the cognitive impaired patients showed higher cerebellar metabolism (p = 0.03), which correlated with more severe deficits in working memory and executive function (p = 0.03). Conclusions: Hypermetabolism in the cerebellum may reflect inefficient brain processing and play a role in cognitive impairments after COVID-19.

KW - brain fog

KW - brain metabolism

KW - cognitive impairment

KW - COVID-19

KW - FDG

KW - PET

KW - positron emission tomography

KW - quality of life

KW - work function

U2 - 10.3390/brainsci13010023

DO - 10.3390/brainsci13010023

M3 - Journal article

C2 - 36672005

AN - SCOPUS:85146820003

VL - 13

JO - Brain Sciences

JF - Brain Sciences

SN - 2076-3425

IS - 1

M1 - 23

ER -

ID: 373028752