Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1
文献类型：期刊论文
| 作者 | Liao, Wei-Ping ; Shi, Yi-Wu ; Long, Yue-Sheng ; Zeng, Yang ; Li, Tian ; Yu, Mei-Juan ; Su, Tao ; Deng, Ping ; Lei, Zhi-Gang ; Xu, Shu-Jun ; Deng, Wei-Yi ; Liu, Xiao-Rong ; Sun, Wei-Wen ; Yi, Yong-Hong ; Xu, Zao C. ; Duan, Shumin |
| 刊名 | EPILEPSIA
 |
| 出版日期 | 2010 |
| 卷号 | 51期号:9页码:1669-1678 |
| ISSN号 | 0013-9580 |
| 关键词 | SCN1A Channelopathy Partial epilepsy Febrile seizures Sodium channel SEVERE MYOCLONIC EPILEPSY NEURONAL SODIUM-CHANNEL FAMILIAL HEMIPLEGIC MIGRAINE TEMPORAL-LOBE EPILEPSY GENERALIZED EPILEPSY SCN1A MUTATIONS NA+ CHANNEL GENE SCN1A INFANCY PLUS |
| 通讯作者 | Liao, WP (reprint author), Guangzhou Med Coll, Inst Neurosci, Key Lab Neurogenet & Channelopathies Guangdong Pr, Chang Gang Dong Rd 250, Guangzhou 510260, Guangdong, Peoples R China,wpliao@tom.com |
| 英文摘要 | P>Purpose: Generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy in infancy (SMEI) are associated with sodium channel alpha-subunit type-1 gene (SCN1A) mutations. Febrile seizures and partial seizures occur in both GEFS+ and SMEI; sporadic onset and seizure aggravation by antiepileptic drugs (AEDs) are features of SMEI. We thus searched gene mutations in isolated cases of partial epilepsy with antecedent FS (PEFS+) that showed seizure aggravations by AEDs. Methods: Genomic DNA from four patients was screened for mutations in SCN1A, SCN2A, SCN1B, and GABRG2 using denaturing high-performance liquid chromatography (dHPLC) and sequencing. Whole-cell patch clamp analysis was used to characterize biophysical properties of two newly defined mutants of Na(v)1.1 in tsA201 cells. Results: Two heterozygous de novo mutations of SCN1A (R946H and F1765L) were detected, which were proven to cause loss of function of Na(v)1.1. When the functional defects of mutants reported previously are compared, it is found that all mutants from PEFS+ have features of loss of function, whereas GEFS+ shows mild dysfunction excluding loss of function, coincident with mild clinical manifestations. PEFS+ is similar to SMEI clinically with possible AED-induced seizure aggravation and biophysiologically with features of loss of function, and different from SMEI by missense mutation without changes in hydrophobicity or polarity of the residues. Conclusions: Isolated milder PEFS+ may associate with SCN1A mutations and loss of function of Na(v)1.1, which may be the basis of seizure aggravation by sodium channel-blocking AEDs. This study characterized phenotypes biologically, which may be helpful in understanding the pathophysiologic basis, and further in management of the disease. |
| 学科主题 | Neurosciences & Neurology |
| 资助信息 | National Nature Science Foundation of China[30600198, 30700247]; Guangdong Natural Science Foundation[06301101, 5300988] |
| 收录类别 | SCI |
| 语种 | 英语 |
| 公开日期 | 2012-07-13 |
| 源URL | [http://ir.sibs.ac.cn/handle/331001/1577]  |
| 专题 | 上海神经科学研究所_神经所(总) |
| 推荐引用方式 GB/T 7714 | Liao, Wei-Ping,Shi, Yi-Wu,Long, Yue-Sheng,et al. Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1[J]. EPILEPSIA,2010,51(9):1669-1678. |
| APA | Liao, Wei-Ping.,Shi, Yi-Wu.,Long, Yue-Sheng.,Zeng, Yang.,Li, Tian.,...&Duan, Shumin.(2010).Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1.EPILEPSIA,51(9),1669-1678. |
| MLA | Liao, Wei-Ping,et al."Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1".EPILEPSIA 51.9(2010):1669-1678. |
入库方式： OAI收割
来源：上海神经科学研究所
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