Department of clinical and experimental epilepsy, UCL Queen Square Institute of Neurology, London, UK.
Departments of Neurology, National Hospital for Neurology and Neurosurgery, London, UK.
Brain Pathol. 2022 Sep;32(5):e13074. doi: 10.1111/bpa.13074. Epub 2022 Apr 27.
Several lines of evidence link deficient serotonin function and SUDEP. Chronic treatment with serotonin reuptake inhibitors (SRIs) reduces ictal central apnoea, a risk factor for SUDEP. Reduced medullary serotonergic neurones, modulators of respiration in response to hypercapnia, were reported in a SUDEP post-mortem series. The amygdala and hippocampus have high serotonergic innervation and are functionally implicated in seizure-related respiratory dysregulation. We explored serotonergic networks in mesial temporal lobe structures in a surgical and post-mortem epilepsy series in relation to SUDEP risk. We stratified 75 temporal lobe epilepsy patients with hippocampal sclerosis (TLE/HS) into high (N = 16), medium (N = 11) and low risk (N = 48) groups for SUDEP based on generalised seizure frequency. We also included the amygdala in 35 post-mortem cases, including SUDEP (N = 17), epilepsy controls (N = 10) and non-epilepsy controls (N = 8). The immunohistochemistry labelling index (LI) and axonal length (AL) of serotonin transporter (SERT)-positive axons were quantified in 13 regions of interest with image analysis. SERT LI was highest in amygdala and subiculum regions. In the surgical series, higher SERT LI was observed in high risk than low risk cases in the dentate gyrus, CA1 and subiculum (p < 0.05). In the post-mortem cases higher SERT LI and AL was observed in the basal and accessory basal nuclei of the amygdala and peri-amygdala cortex in SUDEP compared to epilepsy controls (p < 0.05). Patients on SRI showed higher SERT in the dentate gyrus (p < 0.005) and CA4 (p < 0.05) but there was no difference in patients with or without a psychiatric history. Higher SERT in hippocampal subfields in TLE/HS cases with SUDEP risk factors and higher amygdala SERT in post-mortem SUDEP cases than epilepsy controls supports a role for altered serotonergic networks involving limbic regions in SUDEP. This may be of functional relevance through reduced 5-HT availability.
有几条证据表明,5-羟色胺功能不足与猝倒性睡眠呼吸暂停(SUDEP)有关。慢性使用 5-羟色胺再摄取抑制剂(SSRIs)可减少癫痫发作中的中枢性呼吸暂停,这是 SUDEP 的一个危险因素。在猝倒性睡眠呼吸暂停的尸检系列研究中报道,延髓 5-羟色胺能神经元减少,这些神经元是对高碳酸血症反应的呼吸调节剂。我们在手术和尸检癫痫系列研究中探索了内侧颞叶结构中的 5-羟色胺能网络与猝倒性睡眠呼吸暂停风险的关系。我们根据全面性癫痫发作频率,将 75 例有海马硬化的颞叶癫痫患者(TLE/HS)分为高(N=16)、中(N=11)和低(N=48)风险组用于 SUDEP。我们还纳入了 35 例尸检病例,包括猝倒性睡眠呼吸暂停(SUDEP,N=17)、癫痫对照组(N=10)和非癫痫对照组(N=8),并使用免疫组织化学标记指数(LI)和轴突长度(AL)对 13 个感兴趣区域的 5-羟色胺转运体(SERT)阳性轴突进行了定量分析。SERT LI 在杏仁核和海马旁回区域最高。在手术系列中,高风险组的 SERT LI 高于低风险组,在齿状回、CA1 和海马旁回(p<0.05)。在尸检病例中,与癫痫对照组相比,SUDEP 患者的杏仁基底核和附属基底核以及杏仁周皮质的 SERT LI 和 AL 更高(p<0.05)。服用 SRI 的患者齿状回(p<0.005)和 CA4(p<0.05)的 SERT 更高,但有或没有精神病史的患者之间没有差异。有猝倒性睡眠呼吸暂停风险因素的 TLE/HS 患者的海马亚区 SERT 较高,尸检猝倒性睡眠呼吸暂停患者的杏仁核 SERT 高于癫痫对照组,这支持涉及边缘区域的 5-羟色胺能网络改变在猝倒性睡眠呼吸暂停中的作用。这可能通过降低 5-HT 的可用性而具有功能相关性。