Immediate suppression of seizure clusters by corticosteroids in PCDH19 female epilepsy

被引:44
作者
Higurashi, Norimichi [1 ,2 ]
Takahashi, Yukitoshi [3 ]
Kashimada, Ayako [4 ]
Sugawara, Yuji [4 ]
Sakuma, Hiroshi [5 ]
Tomonoh, Yuko [6 ]
Inoue, Takahito [6 ]
Hoshina, Megumi [7 ]
Satomi, Ruri [8 ]
Ohfu, Masaharu [9 ,10 ]
Itomi, Kazuya [11 ]
Takano, Kyoko [12 ]
Kirino, Tomoko [13 ]
Hirose, Shinichi [2 ,6 ]
机构
[1] Jikei Univ, Sch Med, Dept Pediat, Minami Ku, Tokyo 1058461, Japan
[2] Fukuoka Univ, Cent Res Inst Pathomech Epilepsy, Jonan Ku, Fukuoka 8140180, Japan
[3] Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Aoi Ku, Shizuoka 4208688, Japan
[4] Tokyo Med & Dent Univ, Dept Pediat, Bunkyo Ku, Tokyo 1138510, Japan
[5] Tokyo Metropolitan Inst Med Sci, Dept Brain Dev & Neural Regenerat, Setagaya Ku, Tokyo 1568506, Japan
[6] Fukuoka Univ, Sch Med, Dept Pediat, Jonan Ku, Fukuoka 8140180, Japan
[7] Ohara Gen Hosp, Dept Pediat, Fukushima 9608611, Japan
[8] JA Toride Med Ctr, Dept Pediat, Toride, Ibaraki 3020022, Japan
[9] Okinawa Prefectural Southern Med Ctr, Div Child Neurol, Haebaru, Okinawa 9011193, Japan
[10] Childrens Med Ctr, Haebaru, Okinawa 9011193, Japan
[11] Aichi Childrens Hlth & Med Ctr, Div Neurol, Obu, Aichi 4748710, Japan
[12] Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan
[13] Shikoku Med Ctr Children & Adults, Dept Pediat, Zentsuji, Kagawa 7658507, Japan
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2015年 / 27卷
基金
日本学术振兴会;
关键词
Blood-brain barrier; Epilepsy and mental retardation limited to females (EFMR); Inflammation; Neuronal antibody; N-methyl-D-aspartate (NMDA)-type glutamate receptor; LIMITED EPILEPSY; ANTIBODIES;
D O I
10.1016/j.seizure.2015.02.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: The pathomechanism and treatment of PCDH19 female epilepsy (PCDH19-FE) remain unclear. Here, we report that corticosteroids are effective for control of the seizure clusters or other acute symptoms of PCDH19-FE and argue for the possible involvement of a compromised blood-brain barrier (BBB) in its pathogenesis. Methods: The efficacy of corticosteroids was retrospectively reviewed in five Japanese patients with PCDH19-FE. The results of antibody assays against the N-methyl-D-aspartate-type glutamate receptor (abs-NR) in serum/cerebrospinal fluid were also compiled. Results: Corticosteroid treatments significantly improved the acute symptoms, including seizure clusters, in all cases, most often immediately after the initial administration. However, the effect was transient, and some seizures recurred within a few weeks, especially in association with fever. Serum and/or cerebrospinal fluid abs-NR were detected in all patients. Target sequences of the detected antibodies were multiple, and the titers tended to decrease over time. In one patient, immunohistochemical analysis using rat hippocampal slices also revealed serum antibodies targeting an unknown epitope in neuronal cytoplasm. Conclusion: Our findings imply an involvement of inflammatory processes in the pathogenesis of PCDH19-FE and therapeutic utility for corticosteroids as an adjunctive option in acute treatment. PCDH19 is well expressed in brain microvascular endothelial cells and thus its impairment may cause BBB vulnerability, which may be ameliorated by corticosteroids. The abs-NR detected in our patients may not indicate an autoimmune pathomechanism, but may rather represent non-specific sensitization to degraded neuronal components entering the general circulation, the latter process facilitated by the BBB vulnerability. (C) 2015 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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