Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, UK.
School of Cancer Sciences, University of Southampton, Southampton, UK.
Epilepsia. 2020 Apr;61(4):787-797. doi: 10.1111/epi.16487. Epub 2020 Apr 3.
The "adenosine hypothesis of SUDEP" (sudden unexpected death in epilepsy) predicts that a seizure-induced adenosine surge combined with impaired metabolic clearance can foster lethal apnea or cardiac arrest. Changes in adenosine receptor density and adenosine kinase (ADK) occur in surgical epilepsy patients. Our aim was to correlate the distribution of ADK and adenosine A and A receptors (A R and A R) in surgical tissue from patients with temporal lobe epilepsy and hippocampal sclerosis (TLE/HS) with SUDEP risk factors.
In 75 cases, patients were stratified into high-risk (n = 16), medium-risk (n = 11) and low-risk (n = 48) categories according to the frequency of generalized seizures before surgery. Using whole-slide scanning Definiens image analysis we quantified the labeling index (LI) for ADK, A R, and A R in seven regions of interest: temporal cortex, temporal lobe white matter, CA1, CA4, dentate gyrus, subiculum, and amygdala and relative to glial and neuronal densities with glial fibrillary acidic protein (GFAP) and neuronal nuclear antigen (NeuN).
A R showed predominant neuronal, A R astroglial, and ADK nuclear labeling in all regions but with significant variation. Compared with the low-risk group, the high-risk group had significantly lower A R LI in the temporal cortex. In HS cases with severe neuronal cell loss and gliosis predominantly in the CA1 and CA4 regions, significantly higher A R was present in the amygdala in high-risk than in low-risk cases. There was no significant difference in neuronal loss or gliosis between the risk groups or differences for ADK labeling.
Reduced cortical A R suggests glial dysfunction and impaired adenosine modulation in response to seizures in patients at higher risk for SUDEP. Increased neuronal A R in the high-risk group could contribute to periictal amygdala dysfunction in SUDEP.
“癫痫猝死的腺苷假说”(癫痫发作时的突发性意外死亡)预测,癫痫发作引起的腺苷激增与代谢清除受损会导致致命性呼吸暂停或心脏骤停。手术癫痫患者的腺苷受体密度和腺苷激酶(ADK)发生变化。我们的目的是将颞叶癫痫伴海马硬化(TLE/HS)患者手术组织中 ADK 和腺苷 A 和 A 受体(A R 和 A R)的分布与 SUDEP 的风险因素相关联。
在 75 例病例中,根据术前全身性癫痫发作的频率将患者分为高危组(n=16)、中危组(n=11)和低危组(n=48)。使用全切片扫描 Definiens 图像分析,我们在 7 个感兴趣区域(颞叶皮质、颞叶白质、CA1、CA4、齿状回、下托和杏仁核)量化 ADK、A R 和 A R 的标记指数(LI),并与神经胶质纤维酸性蛋白(GFAP)和神经元核抗原(NeuN)的神经胶质和神经元密度相关。
A R 在所有区域均表现出主要的神经元、A R 星形胶质和 ADK 核标记,但存在显著的变异性。与低危组相比,高危组颞叶皮质的 A R LI 明显降低。在 HS 病例中,CA1 和 CA4 区域的神经元细胞丢失和神经胶质增生严重,高危组的杏仁核中 A R 明显高于低危组。在神经元丢失或神经胶质增生方面,高危组和低危组之间没有显著差异,ADK 标记也没有差异。
在高危患者中,皮质 A R 减少提示癫痫发作时的神经胶质功能障碍和腺苷调节受损。高危组中 A R 的增加可能导致 SUDEP 中的杏仁核功能障碍。