Blümcke Ingmar
Department of Neuropathology, University Hospital Erlangen, Germany.
Free Neuropathol. 2024 Mar 22;5:8. doi: 10.17879/freeneuropathology-2024-5347. eCollection 2024 Jan.
Neuropathology-based studies in neurosurgically resected brain tissue obtained from carefully examined patients with focal epilepsies remain a treasure box for excellent insights into human neuroscience, including avenues to better understand the neurobiology of human brain organization and neuronal hyperexcitability at the cellular level including glio-neuronal interaction. It also allows to translate results from animal models in order to develop personalized treatment strategies in the near future. A nice example of this is the discovery of a new disease entity in 2017, termed mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy or MOGHE, in the frontal lobe of young children with intractable seizures. In 2021, a brain somatic missense mutation of the galactose transporter SLC35A2 leading to altered glycosylation of lipoproteins in the Golgi apparatus was detected in 50 % of MOGHE samples. In 2023, the first clinical trial evaluated galactose supplementation in patients with histopathologically confirmed MOGHE carrying brain somatic mutations that were not seizure free after surgery. The promising results of this pilot trial are an example of personalized medicine in the arena of epileptology. Besides this, neuropathological studies of epilepsy samples have revealed many other fascinating results for the main disease categories in focal epilepsies, such as the first deep-learning based classifier for Focal Cortical Dysplasia, or the genomic landscape of cortical malformations showing new candidate genes such as , which is associated with ganglioglioma and adverse clinical outcome. This update will also ask why common pathogenic variants accumulate in certain brain regions, e.g., in the frontal lobe, and in the temporal lobe. Finally, I will highlight the ongoing discussion addressing commonalities between temporal lobe epilepsy and Alzheimer's disease, the impact of adult neurogenesis and gliogenesis for the initiation and progression of temporal lobe seizures in the human brain as well as the immunopathogenesis of glutamic acid decarboxylase antibody associated temporal lobe epilepsy as a meaningful disease entity. This review will update the reader on some of these fascinating publications from 2022 and 2023 which were selected carefully, yet subjectively, by the author.
对经仔细检查的局灶性癫痫患者的神经外科切除脑组织进行的基于神经病理学的研究,仍然是深入了解人类神经科学的宝库,包括更好地理解人类脑组织神经生物学以及细胞水平上神经元过度兴奋(包括神经胶质-神经元相互作用)的途径。它还能将动物模型的研究结果进行转化,以便在不久的将来制定个性化治疗策略。一个很好的例子是2017年在患有难治性癫痫的幼儿额叶中发现了一种新的疾病实体,称为癫痫伴少突胶质细胞增生的轻度皮质发育畸形(MOGHE)。2021年,在50%的MOGHE样本中检测到半乳糖转运蛋白SLC35A2的脑体细胞错义突变,该突变导致高尔基体中脂蛋白糖基化改变。2023年,首个临床试验评估了对组织病理学确诊为MOGHE且携带脑体细胞突变、术后仍未无癫痫发作的患者补充半乳糖的效果。这项初步试验的可喜结果是癫痫学领域个性化医疗的一个例子。除此之外,对癫痫样本的神经病理学研究还揭示了局灶性癫痫主要疾病类型的许多其他引人入胜的结果,比如首个基于深度学习的局灶性皮质发育不良分类器,或者皮质畸形的基因组图谱显示出与节细胞胶质瘤及不良临床结局相关的新候选基因等。本综述还将探讨为何常见的致病变异会在某些脑区(如额叶和颞叶)积聚。最后,我将重点介绍正在进行的关于颞叶癫痫与阿尔茨海默病之间共性的讨论、成人神经发生和胶质生成对人脑颞叶癫痫发作起始和进展的影响,以及谷氨酸脱羧酶抗体相关颞叶癫痫作为一个有意义的疾病实体的免疫发病机制。本综述将向读者介绍作者精心但主观挑选的2022年和2023年的一些此类引人入胜的出版物。