| Literature DB >> 19679415 |
Naoyuki Tanuma1, Rie Miyata, Satoko Kumada, Masaya Kubota, Jun-ichi Takanashi, Akihisa Okumura, Shin-Ichiro Hamano, Masaharu Hayashi.
Abstract
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a recently clinicoradiologically-established encephalopathy syndrome. In the present study, we examined the levels of cerebrospinal fluid (CSF) tau protein, a marker of axonal damage, in 11 patients with AESD. CSF tau levels were normal on day 1 and increased from day 3 of the disease between the initial and the secondary seizures. Magnetic resonance imaging (MRI) reveals reduced diffusion in the subcortical white matter during days 3-7. Two patients showed elevated tau protein prior to the diffusion abnormality of subcortical white matter on MRI. Levels of CSF neuron specific enolase (NSE), a neuronal marker, were elevated in only two out of seven patients with AESD, and CSF tau levels were also increased in these patients. Our results indicated that tau protein is a more sensitive marker than NSE and axonal damage causes the conspicuous MRI findings in AESD patients. A therapeutic strategy for axonal protection should be developed to prevent severe neurological impairment of AESD patients. Copyright (c) 2009 Elsevier B.V. All rights reserved.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19679415 DOI: 10.1016/j.braindev.2009.07.004
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961