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创伤性脑损伤后致痫发生的新方法。

Novel Approaches to Prevent Epileptogenesis After Traumatic Brain Injury.

机构信息

Department of Neuroscience, Tufts University School of Medicine, Boston, MA, USA.

A. I. Virtanen Institute, University of Eastern Finland, 70 211, Kuopio, Finland.

出版信息

Neurotherapeutics. 2021 Jul;18(3):1582-1601. doi: 10.1007/s13311-021-01119-1. Epub 2021 Sep 30.

Abstract

Traumatic brain injury (TBI) is defined as an alteration in brain function or other evidence of brain pathology caused by an external force. When epilepsy develops following TBI, it is known as post-traumatic epilepsy (PTE). PTE occurs in a subset of patients suffering from different types and severities of TBI, occurs more commonly following severe injury, and greatly impacts the quality of life for patients recovering from TBI. Similar to other types of epilepsy, PTE is often refractory to drug treatment with standard anti-seizure drugs. No therapeutic approaches have proven successful in the clinic to prevent the development of PTE. Therefore, novel treatment strategies are needed to stop the development of PTE and improve the quality of life for patients after TBI. Interestingly, TBI represents an excellent clinical opportunity for intervention to prevent epileptogenesis as typically the time of initiation of epileptogenesis (i.e., TBI) is known, the population of at-risk patients is large, and animal models for preclinical studies of mechanisms and treatment targets are available. If properly identified and treated, there is a true opportunity to prevent epileptogenesis after TBI and stop seizures from ever happening. With that goal in mind, here we review previous attempts to prevent PTE both in animal studies and in humans, we examine how biomarkers could enable better-targeted therapeutics, and we discuss how genetic variation may predispose individuals to PTE. Finally, we highlight exciting new advances in the field that suggest that there may be novel approaches to prevent PTE that should be considered for further clinical development.

摘要

创伤性脑损伤 (TBI) 定义为由于外力导致的脑功能改变或其他脑病理学证据。当 TBI 后出现癫痫时,称为外伤性癫痫 (PTE)。PTE 发生在患有不同类型和严重程度 TBI 的患者亚组中,更常见于严重损伤后,并极大地影响 TBI 患者的生活质量。与其他类型的癫痫一样,PTE 通常对标准抗癫痫药物的药物治疗反应不佳。在临床上,没有任何治疗方法被证明能成功预防 PTE 的发生。因此,需要新的治疗策略来阻止 PTE 的发展并改善 TBI 后患者的生活质量。有趣的是,TBI 为干预提供了一个极好的临床机会,以防止癫痫发生,因为通常可以知道癫痫发生的起始时间(即 TBI),高危患者人群庞大,并且有用于研究机制和治疗靶点的临床前动物模型。如果得到正确的识别和治疗,就有真正的机会在 TBI 后预防癫痫发生,并阻止癫痫发作的发生。考虑到这一目标,我们在这里回顾了以前在动物研究和人类中预防 PTE 的尝试,我们研究了生物标志物如何能够实现更有针对性的治疗,以及我们讨论了遗传变异如何使个体易患 PTE。最后,我们强调了该领域令人兴奋的新进展,这些进展表明可能有预防 PTE 的新方法,应该考虑进一步的临床开发。

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本文引用的文献

1
Acute thalamic damage as a prognostic biomarker for post-traumatic epileptogenesis.
Epilepsia. 2021 Aug;62(8):1852-1864. doi: 10.1111/epi.16986. Epub 2021 Jul 9.
2
In-depth characterization of a mouse model of post-traumatic epilepsy for biomarker and drug discovery.
Acta Neuropathol Commun. 2021 Apr 26;9(1):76. doi: 10.1186/s40478-021-01165-y.
4
Two decades of research towards a potential first anti-epileptic drug.
Seizure. 2021 Aug;90:99-109. doi: 10.1016/j.seizure.2021.02.031. Epub 2021 Mar 3.
5
Neuropathophysiological Mechanisms and Treatment Strategies for Post-traumatic Epilepsy.
Front Mol Neurosci. 2021 Feb 23;14:612073. doi: 10.3389/fnmol.2021.612073. eCollection 2021.
6
Identification of clinically relevant biomarkers of epileptogenesis - a strategic roadmap.
Nat Rev Neurol. 2021 Apr;17(4):231-242. doi: 10.1038/s41582-021-00461-4. Epub 2021 Feb 16.
8
In vivo KPT-350 treatment decreases cortical hyperexcitability following traumatic brain injury.
Brain Inj. 2020 Sep 18;34(11):1489-1496. doi: 10.1080/02699052.2020.1807056. Epub 2020 Aug 27.
10
Modeling Controlled Cortical Impact Injury in 3D Brain-Like Tissue Cultures.
Adv Healthc Mater. 2020 Jun;9(12):e2000122. doi: 10.1002/adhm.202000122. Epub 2020 May 13.

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