Neurology Department, Azienda Ospedaliera-Universitaria di Modena, 41126 Modena, Italy.
PhD Program in Clinical and Experimental Medicine, University of Modena and Reggio-Emilia, 41121 Modena, Italy.
Int J Mol Sci. 2023 Aug 7;24(15):12519. doi: 10.3390/ijms241512519.
As per the latest ILAE definition, status epilepticus (SE) may lead to long-term irreversible consequences, such as neuronal death, neuronal injury, and alterations in neuronal networks. Consequently, there is growing interest in identifying biomarkers that can demonstrate and quantify the extent of neuronal and glial injury. Despite numerous studies conducted on animal models of status epilepticus, which clearly indicate seizure-induced neuronal and glial injury, as well as signs of atrophy and gliosis, evidence in humans remains limited to case reports and small case series. The implications of identifying such biomarkers in clinical practice are significant, including improved prognostic stratification of patients and the early identification of those at high risk of developing irreversible complications. Moreover, the clinical validation of these biomarkers could be crucial in promoting neuroprotective strategies in addition to antiseizure medications. In this study, we present a systematic review of research on biomarkers of neuro-glial injury in patients with status epilepticus.
根据最新的 ILAE 定义,癫痫持续状态 (SE) 可能导致长期不可逆的后果,如神经元死亡、神经元损伤和神经元网络的改变。因此,人们越来越关注寻找能够证明和量化神经元和神经胶质损伤程度的生物标志物。尽管有许多关于癫痫持续状态动物模型的研究,这些研究清楚地表明癫痫发作引起的神经元和神经胶质损伤,以及萎缩和神经胶质增生的迹象,但在人类中,证据仍然仅限于病例报告和小病例系列。在临床实践中识别这些生物标志物的意义重大,包括改善患者的预后分层和早期识别那些有发展为不可逆并发症高风险的患者。此外,这些生物标志物的临床验证对于促进神经保护策略以及抗癫痫药物的应用可能至关重要。在这项研究中,我们对癫痫持续状态患者神经胶质损伤生物标志物的研究进行了系统综述。