Chronic dysfunction of blood-brain barrier in patients with post-encephalitic/encephalopathic epilepsy.

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ID: 100387
2018
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Abstract
This study aimed to elucidate the characteristics and effects of chronic blood-brain barrier (BBB) dysfunction in patients with post-encephalitic/encephalopathic epilepsy (PEE), using brain images and the cerebral spinal fluid (CSF)/serum albumin ratio (albumin quotient, QAlb) as a marker of BBB function.We examined the albumin levels in CSF and serum samples from 312 patients with refractory epilepsy in our center between 2004 and 2015. Sixty samples from patients with PEE and 97 samples from age- and sex-matched disease controls (DC) were evaluated. We classified PEE patients into a widespread lesion group and a focal lesion group by severity on brain magnetic resonance images in the chronic phase after acute encephalitis/encephalopathy.Median QAlb was higher in PEE than in DC [median (range) ×10: PEE 3.6 (1.0-10.3) versus DC 2.7 (1.0-6.7), p = 0.007]. In a linear regression analysis of the relationship between QAlb and patient's age at CSF examination or duration of epilepsy, the slope of the regression line was greater in PEE than in DC. Furthermore, in patients under ten years of age, linear regression analysis of QAlb versus seizure frequency showed a weak but positive correlation. Among PEE patients, seizure frequency was higher in the widespread lesion group than in the focal lesion group [300 (4-3000) versus 30 (1-1500) seizures/month, p <  0.001].Our study suggests that patients with PEE have more severe BBB dysfunction, and that the BBB dysfunction is associated with refractory epilepsy.
Reference Key
kimizu2018chronicseizure Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Kimizu, Tomokazu;Takahashi, Yukitoshi;Oboshi, Taikan;Horino, Asako;Omatsu, Hirowo;Koike, Takayoshi;Yoshitomi, Shinsaku;Yamaguchi, Tokito;Otani, Hideyuki;Ikeda, Hiroko;Imai, Katsumi;Shigematsu, Hideo;Inoue, Yushi;
Journal seizure
Year 2018
DOI
S1059-1311(18)30446-1
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