Highlights
- •Chronic severe traumatic head injury patients have changed brain glucose metabolism.
- •FDG uptake was high in patients with high wakefulness and small ventricular size.
- •Anticonvulsant withdrawal and language expression improved with FDG uptake.
Abstract
Little is known about changes in glucose metabolism in patients with chronic severe
traumatic brain injury (sTBI). It remains to be elucidated how neurological manifestations
of sTBI are associated with brain glucose metabolism during longitudinal follow-up.
We show here that neurological manifestations are associated with changes of brain
glucose metabolism by using two serial 18F-fluorodeoxyglucose positron emission tomography/computed
tomography (18F-FDG PET/CT) images. In this longitudinal observational study, two
serial 18F-FDG PET/CT images from each of 45 patients were analyzed for whole-brain
maximum standardized uptake values (SUVmax). For clinical assessment, we applied two
different scales: the coma recovery scale-revised and the original Chiba score with
additional information regarding nutrition, excretion, facial expression, and position
change of the patient's relative immobility and bedridden state. As a result, the
increased FDG uptake group was associated with a high level of wakefulness (first
PET, p = 0.04; second PET, p = 0.01) and small ventricular size (first PET, p = 0.01; second PET, p = 0.01). In addition, anticonvulsant withdrawal (p = 0.001), improvement of total Chiba score (p = 0.01), language expression (p = 0.03), position change (p = 0.03), and communication (p = 0.03) were accelerated in the increased FDG uptake group. Spearman’s rank correlation
coefficients of change in SUVmax and language expression between the first and second
PET were 0.4 (p = 0.01). Our results indicate that chronic severe traumatic head injury patients
have changed brain glucose metabolism.
Keywords
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Article info
Publication history
Published online: August 29, 2018
Accepted:
August 21,
2018
Received:
April 23,
2018
Identification
Copyright
© 2018 Elsevier Ltd. All rights reserved.