Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Department of Nuclear Medicine, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
CNS Neurosci Ther. 2023 Sep;29(9):2522-2529. doi: 10.1111/cns.14192. Epub 2023 Mar 27.
Ictal piloerection (IP) is an uncommon symptom in focal epilepsy and is associated with autoimmune encephalitis (AE). However, the networks involved in AE-associated IP are still unclear. To have a better understanding of IP underlying mechanisms, the current study investigated whole-brain metabolic networks for the analysis of AE-associated IP.
Patients with AE and IP diagnosed at our Institute between 2018 and 2022 were selected. We then investigated the brain regions associated with AE-associated IP using positron emission tomography (PET). Anatomometabolic changes (interictal F fluorodeoxyglucose PET) in AE patients with IP were compared with those of AE patients of similar age without IP (p-voxel <0.001, uncorrected).
Sixteen patients showed significant IP. The overall IP prevalence was 4.09% of patients with AE and 12.9% of patients with limbic encephalitis. The most common autoantibodies were against LGI1 (68.8%) followed by GAD65 (6.3%), NMDA (6.3%), GABAb (6.3%), CASPR2 (6.3%), and antibodies recognizing both GAD65 and mGLUR5 (6.3%). Most patients responded well to immunotherapy. Analysis of the imaging results at the voxel level showed that patients with IP had hypermetabolic changes in the right inferior temporal gyrus, suggesting involvement of this brain region in IP.
Our findings indicate that IP as an uncommon AE-associated manifestations should be recognized. We observed that the metabolic pattern of IP was conspicuous in the right inferior temporal gyrus.
发作性直立性毛发竖起(IP)是局灶性癫痫中一种不常见的症状,与自身免疫性脑炎(AE)有关。然而,与 AE 相关的 IP 所涉及的网络仍不清楚。为了更好地了解 IP 的潜在机制,本研究通过正电子发射断层扫描(PET)分析了全脑代谢网络。
选择 2018 年至 2022 年在我院诊断为 AE 和 IP 的患者。然后,我们使用正电子发射断层扫描(PET)研究与 AE 相关 IP 相关的脑区。比较了伴有 IP 的 AE 患者和具有相似年龄但无 IP 的 AE 患者的脑区代谢变化(发作间期 F 氟脱氧葡萄糖 PET)(体素 p 值 <0.001,未校正)。
16 例患者出现明显的 IP。AE 患者的总体 IP 患病率为 4.09%,边缘性脑炎患者为 12.9%。最常见的自身抗体是针对 LGI1(68.8%),其次是 GAD65(6.3%)、NMDA(6.3%)、GABAb(6.3%)、CASPR2(6.3%)和同时识别 GAD65 和 mGLUR5 的抗体(6.3%)。大多数患者对免疫治疗反应良好。在体素水平分析影像学结果表明,伴有 IP 的患者右侧下颞叶代谢亢进,提示该脑区参与了 IP。
我们的研究结果表明,作为一种不常见的 AE 相关表现的 IP 应该被识别。我们观察到 IP 的代谢模式在右侧下颞叶很明显。