Alpha-synuclein is a potential biomarker in the serum and CSF of patients with intractable epilepsy

被引:36
作者
Hu, Rong [1 ]
Luo, Jin [1 ]
Wang, Wei [1 ]
Wang, Xuefeng [1 ]
Xi, Zhiqin [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Neurol, Chongqing 400016, Peoples R China
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2015年 / 27卷
关键词
Intractable; Epilepsy; Synuclein; CEREBROSPINAL-FLUID; DISEASE; DEFINITION; DISORDERS; NEURONS;
D O I
10.1016/j.seizure.2015.02.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Intractable epilepsy is a brain disorder characterized by recurrent seizures and intracellular alpha-synuclein (alpha S) deposits; however, the neurobiological basis of this protein accumulation is still poorly understood. This is the first study aiming to assess whether the increase of aS concentrations in the serum and CSF (cerebrospinal fluid) could serve as a marker for aS deposition in the brain and diagnosis of epilepsy. Methods: This investigation enrolled 67 epileptic patients (40 with intractable epilepsy; 13 with newly diagnosed epilepsy, and 14 with non-intractable epilepsy). CSF and serum samples were collected from each patient and were assessed by ELISA. Results: It was established that the concentration of aS in the CSF and serum was elevated in the epilepsy patients, as compared to the control. However, the results of the subgroup analysis revealed that levels of aS in the serum and CSF were increased in the intractable epileptic patients (CSF: 11.12 +/- 4.18 ng/ml; serum: 52.93 +/- 22.11 ng/ml), whereas there was no difference in the groups with the newly diagnosed (CSF: 34.998 +/- 14.96 ng/ml; serum: 7.77 +/- 3.41 ng/ml) and non-intractable epilepsy (CSF: 8.93 +/- 4.83 ng/ml; serum: 34.11 +/- 17.53 ng/ml). Conclusion: Overall, we found that the rise of the aS content in the serum and CSF may facilitate the identification of intractable epilepsy; therefore, the determination of aS rates may serve as a valuable prognostic marker in the clinical assessment. (C) 2015 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6 / 9
页数:4
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