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Chronoepileptology: Mapping the Rhythms of Seizure Risk. 时间癫痫学:绘制癫痫发作风险的节律。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-10-31 DOI: 10.1177/15357597251392099
Christophe Bernard, Gordon F Buchanan, Mohamad Z Koubeissi, Tobias Loddenkemper, Page B Pennell

Seizure occurrence in epilepsy is governed by biological rhythms, challenging the traditional view of seizures as random events. Circadian and multidien cycles shape seizure risk, with patient-specific chronotypes and stable temporal patterns observed across epilepsy types. The Molecular Oscillations and Rhythmicity of Epilepsy hypothesis posits that molecular oscillations-particularly those involving core clock genes and region-specific protein expression-create dynamic windows of increased seizure susceptibility. In epilepsy, these rhythms are altered, amplifying seizure risk through metabolic and genetic reorganization. Seizure timing is also modulated by hormonal cycles in women with catamenial epilepsy. Estrogen promotes seizures, while progesterone and its metabolite allopregnanolone are protective. Three distinct catamenial patterns guide diagnosis and treatment, though evidence for hormonal therapies remains limited. Personalized approaches, including adjunctive medications and cycle-specific dosing, may reduce seizure burden. Importantly, sudden unexpected death in epilepsy predominantly occurs at night, implicating sleep, circadian timing, and environmental factors. Nocturnal vulnerability is conserved across species, suggesting a biological mechanism potentially involving serotonin, which regulates respiration, cardiac function, and arousal. Finally, chronotherapeutic approaches offer a promising avenue for epilepsy management by aligning treatment with seizure timing. Time-adjusted dosing of antiseizure medications has shown improved outcomes in patients with predictable seizure patterns. Future strategies may include closed-loop systems and biomarker-guided interventions to shift seizure susceptibility rhythms. Together, these findings underscore the importance of temporal biology in epilepsy. Understanding when seizures occur provides insight into why they occur, paving the way for personalized, rhythm-informed care that enhances prediction, prevention, and treatment.

癫痫发作是由生物节律控制的,这挑战了癫痫发作是随机事件的传统观点。昼夜节律和多周期影响癫痫发作风险,在不同癫痫类型中观察到患者特有的时间型和稳定的时间模式。癫痫的分子振荡和节律性假说认为,分子振荡——特别是那些涉及核心时钟基因和区域特异性蛋白质表达的分子振荡——创造了增加癫痫易感性的动态窗口。在癫痫中,这些节律被改变,通过代谢和基因重组增加癫痫发作的风险。癫痫发作的时间也由女性的荷尔蒙周期调节。雌激素促进癫痫发作,而孕酮及其代谢物异孕酮具有保护作用。三种不同的羊膜模式指导诊断和治疗,尽管激素治疗的证据仍然有限。个性化的治疗方法,包括辅助用药和周期特异性给药,可以减轻癫痫发作的负担。重要的是,癫痫猝死主要发生在夜间,涉及睡眠、昼夜节律和环境因素。夜间脆弱性在不同物种中都是保守的,这表明一种可能涉及血清素的生物学机制,血清素调节呼吸、心脏功能和觉醒。最后,时间治疗方法为癫痫管理提供了一个有希望的途径,使治疗与癫痫发作时间一致。时间调整剂量的抗癫痫药物已显示出改善的结果,患者可预测的癫痫发作模式。未来的策略可能包括闭环系统和生物标志物引导的干预措施来改变癫痫易感节律。总之,这些发现强调了时间生物学在癫痫中的重要性。了解癫痫发作的发生时间可以深入了解其发生的原因,为个性化、节律知情的护理铺平道路,从而增强预测、预防和治疗。
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引用次数: 0
Temporal Lobe Epilepsy With GAD Antibodies-Time to Give Up, or Time to Double Down? 颞叶癫痫伴广泛性焦虑症抗体:是时候放弃了,还是要加倍努力?
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-10-23 DOI: 10.1177/15357597251386752
Claude Steriade
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引用次数: 0
The Fast and the Very Fast: High-Frequency Oscillations in Alzheimer's Disease. 快和非常快:阿尔茨海默病的高频振荡。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-10-17 DOI: 10.1177/15357597251386661
Manuel Silva-Pérez, Jeannie Chin
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引用次数: 0
Playing Multiple Parts: Unique Enzymatic and Structural Roles Orchestrated by SYNGAP1. 发挥多重作用:由SYNGAP1编排的独特酶和结构作用。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-30 DOI: 10.1177/15357597251377615
Gordon F Buchanan
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引用次数: 0
Resistance is not Futile: Common Genetic Factor Identified for Drug-Resistant Focal Epilepsy. 耐药性不是徒劳的:确定耐药性局灶性癫痫的共同遗传因素。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-21 DOI: 10.1177/15357597251377602
Edward Glasscock
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引用次数: 0
Fire and Ice: Who's the Main Character in FCDII Pathogenesis? 火与冰:谁是FCDII发病机制的主角?
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-15 DOI: 10.1177/15357597251377606
Tong Pan, Louis T Dang
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引用次数: 0
Don't Sleep on It: The Prognostic Value of Electroencephalography (EEG) Spindles in the Critically ill. 不要睡不着觉:脑电图(EEG)纺锤波对危重病人的预后价值。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-15 eCollection Date: 2025-09-01 DOI: 10.1177/15357597251370335
Vineet Punia
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引用次数: 0
Epilepsy Readmissions: The More Things Change the More They Stay the Same. 癫痫再入院:变化越多,它们就越保持不变。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-11 DOI: 10.1177/15357597251372035
Katherine Noe
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引用次数: 0
The Midline Thalamus: The New Kid in Town for Absence Seizure Therapy. 中线丘脑:缺席癫痫治疗的新成员。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-09-01 DOI: 10.1177/15357597251372049
Jeffrey H Goodman
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引用次数: 0
Knockdown-Replace: A New Dynamic for Treatment of Dynamin-1 Related developmental and epileptic encephalopathy (DEE). 敲低替代:动力蛋白-1相关发育性和癫痫性脑病(DEE)治疗的新动态。
IF 6.3 2区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2025-08-19 DOI: 10.1177/15357597251370432
Jacy L Wagnon
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引用次数: 0
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Epilepsy Currents
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