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Epilepsy and migraine-Are they comorbidity?癫痫与偏头痛——它们是共病吗?
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引用本文的文献

1
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Association between migraine and epilepsy: a meta-analysis.偏头痛与癫痫之间的关联:一项荟萃分析。
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Front Neurol. 2023 Jul 6;14:1182304. doi: 10.3389/fneur.2023.1182304. eCollection 2023.
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Association of patent foramen ovale with epilepsy: A hospital-based case-control study.卵圆孔未闭与癫痫的相关性:一项基于医院的病例对照研究。
Epilepsia Open. 2023 Sep;8(3):1075-1083. doi: 10.1002/epi4.12787. Epub 2023 Jul 16.
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Epilepsy and Migraine Shared Genetic and Molecular Mechanisms: Focus on Therapeutic Strategies.癫痫与偏头痛的共同遗传和分子机制:聚焦治疗策略
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Serum levels of allopregnanolone, progesterone and testosterone in menstrually-related and postmenopausal migraine: A cross-sectional study.经期相关和绝经后偏头痛患者血清中别孕烯醇酮、孕酮和睾酮的水平:一项横断面研究。
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Comorbid and co-occurring conditions in migraine and associated risk of increasing headache pain intensity and headache frequency: results of the migraine in America symptoms and treatment (MAST) study.偏头痛的共病和合并症及相关的头痛疼痛强度和头痛频率增加的风险:美国偏头痛症状和治疗(MAST)研究的结果。
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本文引用的文献

1
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.由一种新型SCN1A突变引起的早发性家族性偏瘫性偏头痛。
Cephalalgia. 2016 Nov;36(13):1238-1247. doi: 10.1177/0333102415608360. Epub 2016 Jul 11.
2
CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.CACNA1A基因单倍体不足会导致认知障碍、自闭症以及伴有轻度小脑症状的癫痫性脑病。
Eur J Hum Genet. 2015 Nov;23(11):1505-12. doi: 10.1038/ejhg.2015.21. Epub 2015 Mar 4.
3
Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum.癫痫中可挽救的折叠缺陷型 NaV1.1 (SCN1A) 突变体:特性、发生及靶向内质网的肽类的新挽救策略。
Neurobiol Dis. 2015 Mar;75:100-14. doi: 10.1016/j.nbd.2014.12.028. Epub 2015 Jan 6.
4
Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice.1型家族性偏瘫性偏头痛突变的Cav2.1钙通道改变小鼠外侧上橄榄核的抑制性和兴奋性突触传递。
Hear Res. 2015 Jan;319:56-68. doi: 10.1016/j.heares.2014.11.006. Epub 2014 Dec 4.
5
Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutation.在携带人类Na(V)1.1突变的癫痫小鼠模型中,GABA能中间神经元的动作电位起始受损会导致网络过度兴奋。
J Neurosci. 2014 Nov 5;34(45):14874-89. doi: 10.1523/JNEUROSCI.0721-14.2014.
6
Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i.突变型 Cav2.1 通道在家族性偏瘫性偏头痛小鼠模型中的突触效能增强作用归因于基础 [Ca2+]i 的增加。
J Neurosci. 2014 May 21;34(21):7047-58. doi: 10.1523/JNEUROSCI.2526-13.2014.
7
Two novel SCN1A mutations identified in families with familial hemiplegic migraine.在家族性偏瘫性偏头痛家族中鉴定出两种新的SCN1A突变。
Cephalalgia. 2014 Nov;34(13):1062-9. doi: 10.1177/0333102414529195. Epub 2014 Apr 4.
8
Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models.无结构性脑异常的遗传性癫痫综合征:临床特征与实验模型
Neurotherapeutics. 2014 Apr;11(2):269-85. doi: 10.1007/s13311-014-0267-0.
9
Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.L263V SCN1A突变所致家族性偏瘫性偏头痛:杜罗河谷两个家族在癫痫方面的不一致性。
Cephalalgia. 2014 Oct;34(12):1015-20. doi: 10.1177/0333102414527015. Epub 2014 Mar 19.
10
Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.钙通道电压依赖性 α1A 亚基(CACNA1A)和 ATP 酶 Na+/K+ 转运体亚单位α2(ATP1A2)基因在偏瘫型偏头痛中的筛查:临床、遗传和功能研究。
Mol Genet Genomic Med. 2013 Nov;1(4):206-22. doi: 10.1002/mgg3.24. Epub 2013 Jul 2.

癫痫与偏头痛——它们是共病吗?

Epilepsy and migraine-Are they comorbidity?

作者信息

Liao Jin, Tian Xin, Wang Hao, Xiao Zheng

机构信息

Neurology Department at Chongqing Medical University, Chongqing, China.

Neurology Department at the First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Street, Yuanjiagang, Yuzhong District, Chongqing, China.

出版信息

Genes Dis. 2018 May 5;5(2):112-118. doi: 10.1016/j.gendis.2018.04.007. eCollection 2018 Jun.

DOI:10.1016/j.gendis.2018.04.007
PMID:30258939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6146266/
Abstract

Epilepsy and migraine often co-occur. From the clinical symptoms, they often have some signs of symptoms before onset; from the pathogenesis of epilepsy and migraine, both of them have a high degree of neuronal excitement and ion channel abnormalities; in terms of treatment, many antiepileptic drugs are work in migraine. All of this indicates that they interact with each other. But it is undeniable that there are interactions and relationships between them, and there are also some differences such as the different clinical episodes, the different ways of neuronal haperexcitability and the different drug treatment programs. And are they comorbidity? If we can better understand the correlation between seizures and migraines, then this will help develop better guidelines for clinical diagnosis and treatment.

摘要

癫痫和偏头痛常同时出现。从临床症状来看,它们在发作前往往有一些症状迹象;从癫痫和偏头痛的发病机制而言,二者都存在高度的神经元兴奋和离子通道异常;在治疗方面,许多抗癫痫药物对偏头痛有效。所有这些都表明它们相互影响。但不可否认的是,它们之间存在相互作用和关系,也存在一些差异,如临床发作不同、神经元过度兴奋的方式不同以及药物治疗方案不同。那么它们是共病吗?如果我们能更好地理解癫痫发作与偏头痛之间的关联,那么这将有助于制定更好的临床诊断和治疗指南。