The cerebral network of COVID-19-related encephalopathy. A longitudinal voxel-based 18F-FDG-PET study
Creators
- 1. Sorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Service de Médecine Nucléaire and LIB, INSERM U1146, 75013, Paris (France)
- 2. Département de Neuroradiologie, Sorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, 75013, Paris (France)
- 3. Département de Neurologie, Sorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, 75013, Paris (France)
- 4. Service de Maladies infectieuses et Tropicales, Sorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, 75013, Paris (France)
- 5. Sorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Institut de la Mémoire et de la Maladie d'Alzheimer, 75013, Paris (France)
Description
Little is known about the neuronal substrates of neuropsychiatric symptoms associated with COVID-19 and their evolution during the course of the disease. We aimed at describing the longitudinal brain metabolic pattern in COVID-19-related encephalopathy using 18F-FDG-PET/CT. Seven patients with variable clinical presentations of COVID-19-related encephalopathy were explored thrice with brain 18F-FDG-PET/CT, once in the acute phase, 1 month later and 6 months after COVID-19 onset. PET images were analysed with voxel-wise and regions-of-interest approaches in comparison with 32 healthy controls. Patients' neurological manifestations during acute encephalopathy were heterogeneous. However, all of them presented with predominant cognitive and behavioural frontal disorders. SARS-CoV-2 RT-PCR in the CSF was negative for all patients. MRI revealed no specific abnormalities for most of the subjects. All patients had a consistent pattern of hypometabolism in a widespread cerebral network including the frontal cortex, anterior cingulate, insula and caudate nucleus. Six months after COVID-19 onset, the majority of patients clinically had improved but cognitive and emotional disorders of varying severity remained with attention/executive disabilities and anxio-depressive symptoms, and lasting prefrontal, insular and subcortical 18F-FDG-PET/CT abnormalities. The implication of this widespread network could be the neural substrate of clinical features observed in patients with COVID-19, such as frontal lobe syndrome, emotional disturbances and deregulation of respiratory failure perception. This study suggests that this network remains mildly to severely impaired 6 months after disease onset.
Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 48
- Journal Issue
- 8
- Journal Page Range
- p. 2543-2557
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 52103882
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BEHAVIOR; BLOOD-BRAIN BARRIER; BRAIN; COMPARATIVE EVALUATIONS; CORONAVIRUSES; FLUORINE 18; FLUORODEOXYGLUCOSE; IMAGE PROCESSING; METABOLISM; NERVOUS SYSTEM DISEASES; NMR IMAGING; POLYMERASE CHAIN REACTION; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RELAXATION TIME; RESPIRATION; RESPIRATORY SYSTEM DISEASES; SYMPTOMS; WEIGHTING FUNCTIONS
- Descriptors DEC
- ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CENTRAL NERVOUS SYSTEM; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; EVALUATION; FLUORINE ISOTOPES; FUNCTIONS; GENE AMPLIFICATION; HOURS LIVING RADIOISOTOPES; INFECTIOUS DISEASES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MICROORGANISMS; NANOSECONDS LIVING RADIOISOTOPES; NERVOUS SYSTEM; NUCLEI; ODD-ODD NUCLEI; ORGANS; PARASITES; PROCESSING; RADIOACTIVE MATERIALS; RADIOISOTOPES; TOMOGRAPHY; VIRAL DISEASES; VIRUSES; ZOONOTIC DISEASES
Optional Information
- Collaborations
- CoCo-Neurosciences study group