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头皮 HFO 率随病灶增大而升高。

Scalp HFO rates are higher for larger lesions.

机构信息

Department of Neuropediatrics, University Children's Hospital Zurich, Zurich, Switzerland.

MR-Research Centre, University Children's Hospital Zurich, Zurich, Switzerland.

出版信息

Epilepsia Open. 2022 Sep;7(3):496-503. doi: 10.1002/epi4.12596. Epub 2022 May 6.

Abstract

High-frequency oscillations (HFO) in scalp EEG are a new and promising noninvasive epilepsy biomarker, providing added prognostic value, particularly in pediatric lesional epilepsy. However, it is unclear if lesion characteristics, such as lesion volume, depth, type, and localization, impact scalp HFO rates. We analyzed scalp EEG from 13 children and adolescents with focal epilepsy associated with focal cortical dysplasia (FCD), low-grade tumors, or hippocampal sclerosis. We applied a validated automated detector to determine HFO rates in bipolar channels. We identified the lesion characteristics in MRI. Larger lesions defined by MRI volumetric analysis corresponded to higher cumulative scalp HFO rates (P = .01) that were detectable in a higher number of channels (P = .05). Both superficial and deep lesions generated HFO detectable in the scalp EEG. Lesion type (FCD vs tumor) and lobar localization (temporal vs extratemporal) did not affect scalp HFO rates in our study. Our observations support that all lesions may generate HFO detectable in scalp EEG, irrespective of their characteristics, whereas larger epileptogenic lesions generate higher scalp HFO rates over larger areas that are thus more accessible to detection. Our study provides crucial insight into scalp HFO detectability in pediatric lesional epilepsy, facilitating their implementation as an epilepsy biomarker in a clinical setting.

摘要

头皮 EEG 的高频振荡(HFO)是一种新的有前途的非侵入性癫痫生物标志物,提供了额外的预后价值,特别是在儿科病变性癫痫中。然而,尚不清楚病变特征,如病变体积、深度、类型和定位,是否会影响头皮 HFO 率。我们分析了 13 名患有局灶性癫痫的儿童和青少年的头皮 EEG,这些癫痫与局灶性皮质发育不良(FCD)、低级别肿瘤或海马硬化有关。我们应用了一种经过验证的自动探测器来确定双极通道中的 HFO 率。我们在 MRI 中确定了病变特征。MRI 体积分析定义的较大病变与较高的累积头皮 HFO 率相关(P=.01),并且可以在更多的通道中检测到(P=.05)。无论是浅层还是深层病变,都可以在头皮 EEG 中产生可检测到的 HFO。病变类型(FCD 与肿瘤)和脑叶定位(颞叶与颞外)在我们的研究中并不影响头皮 HFO 率。我们的观察结果支持所有病变都可能产生可在头皮 EEG 中检测到的 HFO,而不论其特征如何,较大的致痫性病变在更大的区域产生更高的头皮 HFO 率,因此更容易检测到。我们的研究为儿科病变性癫痫中头皮 HFO 的可检测性提供了重要的见解,有助于将其作为癫痫生物标志物在临床环境中实施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/634c/9436296/ccb76bd48196/EPI4-7-496-g002.jpg

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