Evidence of Impaired Neuroimmune System in Post-COVID Syndrome-A Whole Brain Magnetic Resonance Spectroscopy Study.

Evidence of Impaired Neuroimmune System in Post-COVID Syndrome-A Whole Brain Magnetic Resonance Spectroscopy Study.

Publication date: Dec 01, 2025

Chronic fatigue, mood disturbances, and cognitive deficits characterize the neurological post-COVID syndrome (PCS). This study aimed to find out if PCS shows a diagnostic brain metabolic pattern that might also support clarification of the PCS pathology. Whole brain proton magnetic resonance spectroscopy imaging (wbMRSI) was applied to assess brain metabolites in PCS patients. Patients’ data were compared to those of matched healthy controls examined before the COVID pandemic. Patients underwent clinical and neuropsychological assessment and filled in self-report questionnaires related to fatigue, mood, and health-related quality of life. Thirty PCS patients were enrolled into the study. WbMRSI showed significantly reduced levels of brain myo-inositol, which is considered as representative of astrocyte and microglia activity, in the frontal, temporal and parietal lobes, bilaterally, and in the cerebellum of the patients compared to controls. Patients’ creatine was higher in the left frontal lobe and the combined glutamate/glutamine peak was lower in the right parietal lobe. N-acetyl-aspartate, an indicator of neuronal integrity, as well as choline that reflects cell membrane turnover, showed no group differences. The findings suggest an alteration of the neuroimmune system in PCS patients, without indication of disturbed neuronal integrity or alteration of the cerebral energy metabolism.

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Concepts Keywords
Covid Adult
Healthy Aged
Neuroimmune Aspartic Acid
Thirty Aspartic Acid
Wbmrsi Brain
Choline
Choline
cognitive function
COVID-19
Creatine
Creatine
Fatigue
Female
follow‐up
Humans
Inositol
Inositol
Magnetic Resonance Spectroscopy
Male
Middle Aged
N-acetylaspartate
neuroimmune system
post‐COVID
SARS-CoV-2
whole brain MRS

Semantics

Type Source Name
disease MESH Syndrome
disease MESH PCS
disease MESH fatigue
drug DRUGBANK Inositol
drug DRUGBANK Creatine
drug DRUGBANK L-Glutamine
drug DRUGBANK Choline
pathway REACTOME Metabolism
disease MESH Long Covid
disease MESH MRS
disease MESH severe acute respiratory syndrome
disease MESH infections
disease MESH COVID19
disease MESH dys
disease MESH memory deficits
disease MESH headaches
disease MESH anxiety
pathway REACTOME Reproduction
disease MESH hypoxia
drug DRUGBANK Water
pathway REACTOME Glucose metabolism
disease MESH atrophy
disease MESH gliosis
disease MESH brain fog
disease MESH brain metabolic disorder
disease MESH hypertension
disease MESH obesity
disease MESH cognitive impairments
disease MESH included
disease MESH FIS
disease MESH taste disorder
disease MESH insomnia
disease MESH ache
disease MESH myalgia
disease MESH paresthesia
drug DRUGBANK Flunarizine
drug DRUGBANK 1-naphthaleneacetic acid
disease MESH RPL
drug DRUGBANK Methionine
disease MESH IBM
drug DRUGBANK Cysteamine
drug DRUGBANK Tretamine
disease MESH plan
drug DRUGBANK gamma-Aminobutyric acid
drug DRUGBANK Glutathione
disease MESH neuroinflammatory diseases
disease MESH neurodegenerative diseases
pathway REACTOME Neurodegenerative Diseases
disease MESH Alzheimer’s disease
disease MESH Bipolar disorder
disease MESH liver cirrhosis
disease MESH hepatic encephalopathy
disease MESH hyponatremia
disease MESH psychosis
disease MESH chronic infection
disease MESH death
drug DRUGBANK Dextrose unspecified form
disease MESH encephalopathy
drug DRUGBANK Iron
disease MESH Infectious Diseases
disease MESH Inflammation
disease MESH Temporal Lobe Epilepsy
disease MESH Parkinson’s Disease
disease MESH Ischemia
disease MESH Hepatitis
disease MESH Virus Infection
disease MESH Cirrhosis
disease MESH Graves’ Disease
disease MESH Neurological Manifestations
drug DRUGBANK Ammonia
drug DRUGBANK Hyaluronic acid
drug DRUGBANK L-Aspartic Acid

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