Drug-resistant juvenile myoclonic epilepsy: A literature review

IF 2.8 4区 医学 Q2 CLINICAL NEUROLOGY
A. Nica
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引用次数: 0

Abstract

The ILAE's Task Force on Nosology and Definitions revised in 2022 its definition of juvenile myoclonic epilepsy (JME), the most common idiopathic generalized epilepsy disorder, but this definition may well change again in the future. Although good drug response could almost be a diagnostic criterion for JME, drug resistance (DR) is observed in up to a third of patients. It is important to distinguish this from pseudoresistance, which is often linked to psychosocial problems or psychiatric comorbidities. After summarizing these aspects and the various definitions applied to JME, the present review lists the risk factors for DR-JME that have been identified in numerous studies and meta-analyses. The factors most often cited are absence seizures, young age at onset, and catamenial seizures. By contrast, photosensitivity seems to favor good treatment response, at least in female patients. Current hypotheses on DR mechanisms in JME are based on studies of either simple (e.g., cortical excitability) or more complex (e.g., anatomical and functional connectivity) neurophysiological markers, bearing in mind that JME is regarded as a neural network disease. This research has revealed correlations between the intensity of some markers and DR, and above all shed light on the role of these markers in associated neurocognitive and neuropsychiatric disorders in both patients and their siblings. Studies of neurotransmission have mainly pointed to impaired GABAergic inhibition. Genetic studies have generally been inconclusive. Increasing restrictions have been placed on the use of valproate, the standard antiseizure medication for this syndrome, owing to its teratogenic and developmental risks. Levetiracetam and lamotrigine are prescribed as alternatives, as is vagal nerve stimulation, and there are several other promising antiseizure drugs and neuromodulation methods. The development of better alternative treatments is continuing to take place alongside advances in our knowledge of JME, as we still have much to learn and understand.

耐药性青少年肌阵挛性癫痫:文献综述。
国际癫痫学会(ILAE)命名与定义工作组于2022年修订了青少年肌阵挛性癫痫(JME)的定义,这是一种最常见的特发性全身性癫痫疾病,但这一定义在未来很可能会再次改变。虽然良好的药物反应几乎可以作为 JME 的诊断标准,但多达三分之一的患者会出现耐药性(DR)。重要的是要将其与假性耐药性区分开来,后者通常与社会心理问题或精神并发症有关。本综述在总结了这些方面以及适用于 JME 的各种定义后,列出了在大量研究和荟萃分析中发现的 DR-JME 风险因素。最常被引用的因素是失神发作、发病年龄小和惊厥发作。相比之下,光敏性似乎有利于良好的治疗反应,至少在女性患者中是如此。考虑到 JME 被认为是一种神经网络疾病,目前关于 JME 中 DR 机制的假设是基于对简单(如皮层兴奋性)或更复杂(如解剖和功能连接)的神经生理学标志物的研究。这项研究揭示了某些标记物的强度与 DR 之间的相关性,最重要的是揭示了这些标记物在患者及其兄弟姐妹的相关神经认知和神经精神障碍中的作用。对神经传递的研究主要指向 GABA 能抑制受损。遗传学研究通常没有定论。丙戊酸钠是治疗该综合征的标准抗癫痫药物,但由于其致畸和发育风险,该药物的使用受到越来越多的限制。左乙拉西坦和拉莫三嗪可作为替代药物,迷走神经刺激疗法也可作为替代药物,还有其他一些抗癫痫药物和神经调节方法也很有前景。在开发更好的替代治疗方法的同时,我们对 JME 的认识也在不断进步,因为我们还有很多东西需要学习和了解。
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来源期刊
Revue neurologique
Revue neurologique 医学-临床神经学
CiteScore
4.80
自引率
0.00%
发文量
598
审稿时长
55 days
期刊介绍: The first issue of the Revue Neurologique, featuring an original article by Jean-Martin Charcot, was published on February 28th, 1893. Six years later, the French Society of Neurology (SFN) adopted this journal as its official publication in the year of its foundation, 1899. The Revue Neurologique was published throughout the 20th century without interruption and is indexed in all international databases (including Current Contents, Pubmed, Scopus). Ten annual issues provide original peer-reviewed clinical and research articles, and review articles giving up-to-date insights in all areas of neurology. The Revue Neurologique also publishes guidelines and recommendations. The Revue Neurologique publishes original articles, brief reports, general reviews, editorials, and letters to the editor as well as correspondence concerning articles previously published in the journal in the correspondence column.
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