Wang Yihe, Feng Tao, Xiao Fenglai, Yang Yanfeng, Fleury Marine N, Binding Lawrence P, Giampiccolo Davide, Taylor Peter, Koepp Matthias J, Duncan John S, Wei Penghu, Shan Yongzhi, Zhao Guoguang
Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.
Epilepsia. 2025 Aug;66(8):2853-2863. doi: 10.1111/epi.18438. Epub 2025 Apr 29.
Hypothalamic hamartomas (HHs) are developmental malformations associated with focal epilepsy. We investigated the patterns of gray matter morphology and cerebral metabolism in individuals with HHs, with and without focal to bilateral tonic-clonic seizures (FBTCSs), aiming to clarify the accompanying network abnormalities.
We analyzed magnetic resonance imaging (MRI) and fluorodeoxyglucose positron emission tomography (PET) data from 59 patients with HHs (28 with FBTCSs, 31 without), as well as MRI data from 30 healthy controls (HCs) and PET data from 45 HCs. We assessed gray matter voxel-based morphometry and quantitative analysis of cerebral glucose uptake in HH patients and controls, with age, sex, and total intracranial volume as covariates, and drew correlations with duration of epilepsy and seizure semiology and frequency.
Compared to HCs, HH patients had significantly increased gray matter volume (GMV) in the ipsilateral amygdala, piriform cortex, hypothalamus, and bilateral temporal cortices; patients with FBTCSs primarily showed increased GMV in the HH stalk, whereas those without FBTCSs showed increased GMV prominently in the amygdala. GMVs of amygdala and piriform cortex were greater and the ipsilateral midtemporal cortex was more hypometabolic the longer the duration of epilepsy and the greater the seizure frequency. No significant GMV or cerebral glucose uptake differences were found between HH patients with and without FBTCSs.
HH-related epilepsy is a network disorder characterized by widespread abnormalities beyond the lesion. This highlights the importance of considering the whole network when formulating diagnosis and treatment plans.
下丘脑错构瘤(HHs)是与局灶性癫痫相关的发育畸形。我们研究了患有HHs的个体(有和没有继发全面性强直-阵挛发作(FBTCSs))的灰质形态和脑代谢模式,旨在阐明伴随的网络异常。
我们分析了59例HHs患者(28例有FBTCSs,31例无)的磁共振成像(MRI)和氟脱氧葡萄糖正电子发射断层扫描(PET)数据,以及30名健康对照(HCs)的MRI数据和45名HCs的PET数据。我们评估了HH患者和对照基于体素的灰质形态计量学和脑葡萄糖摄取的定量分析,将年龄、性别和总颅内体积作为协变量,并与癫痫持续时间、发作症状学和发作频率进行相关性分析。
与HCs相比,HH患者同侧杏仁核、梨状皮质、下丘脑和双侧颞叶皮质的灰质体积(GMV)显著增加;有FBTCSs的患者主要表现为HH蒂部GMV增加,而没有FBTCSs的患者则主要表现为杏仁核GMV增加。癫痫持续时间越长、发作频率越高,杏仁核和梨状皮质的GMV越大,同侧颞中皮质代谢越低。有和没有FBTCSs的HH患者之间未发现显著的GMV或脑葡萄糖摄取差异。
HH相关癫痫是一种网络障碍,其特征是病变以外广泛存在异常。这突出了在制定诊断和治疗计划时考虑整个网络的重要性。