Struck Aaron F, Westover M Brandon, Hall Lance T, Deck Gina M, Cole Andrew J, Rosenthal Eric S
Department of Neurology, Massachusetts General Hospital (MGH), 55 Fruit Street, Wang 735, Boston, MA, 02114, USA.
Department of Radiology, University of Wisconsin, Madison, WI, USA.
Neurocrit Care. 2016 Jun;24(3):324-31. doi: 10.1007/s12028-016-0245-y.
Ictal-interictal continuum (IIC) continuous EEG (cEEG) patterns including periodic discharges and rhythmic delta activity are associated with poor outcome and in the appropriate clinical context, IIC patterns may represent "electroclinical" status epilepticus (SE). To clarify the significance of IIC patterns and their relationship to "electrographic" SE, we investigated FDG-PET imaging as a complementary metabolic biomarker of SE among patients with IIC patterns.
A single-center prospective clinical database was ascertained for patients undergoing FDG-PET during cEEG. Following MRI-PET co-registration, the maximum standardized uptake value in cortical and subcortical regions was compared to contralateral homologous and cerebellar regions. Consensus cEEG review and clinical rating of etiology and treatment response were performed retrospectively with blinding. Electrographic SE was classified as discrete seizures without interictal recovery or >3-Hz rhythmic IIC patterns. Electroclinical SE was classified as IIC patterns with electrographic and clinical response to anticonvulsants; clonic activity; or persistent post-ictal encephalopathy.
Eighteen hospitalized subjects underwent FDG-PET during contemporaneous IIC patterns attributed to structural lesions (44 %), neuroinflammatory/neuroinfectious disease (39 %), or epilepsy (11 %). FDG-PET hypermetabolism was common (61 %) and predicted electrographic or electroclinical SE (sensitivity 79 % [95 % CI 53-93 %] and specificity 100 % [95 % CI 51-100 %]; p = 0.01). Excluding electrographic SE, hypermetabolism also predicted electroclinical SE (sensitivity 80 % [95 % CI 44-94 %] and specificity 100 % [95 % CI 51-100 %]; p = 0.01).
In hospitalized patients with IIC EEG patterns, FDG-PET hypermetabolism is common and is a candidate metabolic biomarker of electrographic SE or electroclinical SE.
发作期-发作间期连续体(IIC)的连续性脑电图(cEEG)模式,包括周期性放电和节律性δ活动,与不良预后相关,在适当的临床背景下,IIC模式可能代表“电临床”癫痫持续状态(SE)。为了阐明IIC模式的意义及其与“脑电图”SE的关系,我们研究了氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET)成像作为IIC模式患者中SE的一种补充代谢生物标志物。
确定了一个单中心前瞻性临床数据库,纳入在cEEG期间接受FDG-PET检查的患者。在磁共振成像-正电子发射断层扫描(MRI-PET)配准后,将皮质和皮质下区域的最大标准化摄取值与对侧同源区域和小脑区域进行比较。对cEEG进行回顾性共识分析,并对病因和治疗反应进行临床评分,过程中设盲。脑电图SE分为无发作间期恢复的离散发作或>3Hz的节律性IIC模式。电临床SE SE分为对惊厥药物有脑电图和临床反应的IIC模式、阵挛活动或持续性发作后脑病。
18名住院患者在同期IIC模式期间接受了FDG-PET检查,这些模式归因于结构性病变(44%)、神经炎症/神经感染性疾病(39%)或癫痫(11%)。FDG-PET高代谢很常见(61%),并可预测脑电图或电临床SE(敏感性79%[95%CI 53-93%],特异性100%[95%CI 51-100%];p = 0.01)。排除脑电图SE后,高代谢也可预测电临床SE(敏感性80%[95%CI 44-94%],特异性100%[95%CI 51-100%];p = 0.01)。
在有IIC脑电图模式的住院患者中,FDG-PET高代谢很常见,是脑电图SE或电临床SE的一种候选代谢生物标志物。