2020
DOI: 10.1016/j.jns.2019.116636
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Prognostic value of MR spectroscopy in patients with acute excitotoxic encephalopathy

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Cited by 14 publications
(11 citation statements)
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“…Increased levels of Myo-Inositol (mI) may reflect neuroinflammation, which when coupled with choline elevations in demyelinating pathologies may reflect glial proliferation. 18 The presence of elevated Glx levels has been reported in cases of acute excitotoxic leukoencephalopathy 19 and viral-associated acute leukoencephalopathy with restricted diffusion. 20 Both conditions are thought to be mediated by excitotoxic injury to the cerebral white matter and exhibit prominent reduced diffusivity within white matter lesions.…”
Section: Discussionmentioning
confidence: 98%
“…Increased levels of Myo-Inositol (mI) may reflect neuroinflammation, which when coupled with choline elevations in demyelinating pathologies may reflect glial proliferation. 18 The presence of elevated Glx levels has been reported in cases of acute excitotoxic leukoencephalopathy 19 and viral-associated acute leukoencephalopathy with restricted diffusion. 20 Both conditions are thought to be mediated by excitotoxic injury to the cerebral white matter and exhibit prominent reduced diffusivity within white matter lesions.…”
Section: Discussionmentioning
confidence: 98%
“…Tighter control of seizures with EEG monitoring might have suppressed excitotoxicity and the development of AE. Indeed, prolonged seizures cause excitotoxicity [ 24 ], and the association of excitotoxicity with the pathophysiology of AE, such as AESD, has been reported [ 25 , 26 ].…”
Section: Discussionmentioning
confidence: 99%
“…Increased ATP synthesis results in a decrease in phosphocreatine and an increase in Cr levels in these cells. Creatine/phosphocreatine peaks decreased in subcortical white matter in magnetic resonance spectroscopy in patients with AESD with mild to severe sequelae within 7 days of onset ( 15 ). Early seizures in AESD require more ATP synthesis than FS, whereas elevated Cr levels in the brain might be released into the systemic circulation because of the disrupted blood brain barrier in AESD ( 16 ).…”
Section: Discussionmentioning
confidence: 99%