Charité - Universitätsmedizin Berlin, Department of Neurology, Berlin, Germany; Department of Psychology, Humboldt-Universität zu Berlin, Berlin, Germany.
Charité - Universitätsmedizin Berlin, Department of Neurology, Berlin, Germany; German Center for Neurodegenerative Diseases (DZNE), Berlin, Germany.
Neuroimage Clin. 2020;28:102515. doi: 10.1016/j.nicl.2020.102515. Epub 2020 Nov 27.
Hippocampal damage and associated cognitive deficits are frequently observed in neuroimmunological disorders, but comparative analyses to identify shared hippocampal damage patterns are missing. Here, we adopted a transdiagnostic analytical approach and investigated hippocampal shape deformations and associated cognitive deficits in four neuroimmunological diseases. We studied 120 patients (n = 30 in each group), including patients with multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD), anti-NMDAR and anti-LGI1 encephalitis. A control group was matched to each patient sample from a pool of 79 healthy participants. We performed an MRI-based vertex-wise hippocampal shape analysis, extracted hippocampal volume estimates and scalar projection values as a measure of surface displacement. Cognitive testing included assessment of verbal memory and semantic fluency performance. Our cross-sectional analyses revealed characteristic patterns of bilateral inward deformations covering up to 32% of the hippocampal surface in MS, anti-NMDAR encephalitis, and anti-LGI1 encephalitis, whereas NMOSD patients showed no deformations compared to controls. Significant inversions were noted mainly on the hippocampal head, were accompanied by volume loss, and correlated with semantic fluency scores and verbal episodic memory in autoimmune encephalitis and MS. A deformation overlap analysis across disorders revealed a convergence zone on the left anterior hippocampus that corresponds to the CA1 subfield. This convergence zone indicates a shared downstream substrate of immune-mediated damage that appears to be particularly vulnerable to neuroinflammatory processes. Our transdiagnostic morphological view sheds light on mutual pathophysiologic pathways of cognitive deficits in neuroimmunological diseases and stimulates further research into the mechanisms of increased susceptibility of the hippocampus to autoimmunity.
海马损伤及相关认知缺陷在神经免疫性疾病中经常观察到,但缺乏比较分析以确定共同的海马损伤模式。在这里,我们采用了一种跨诊断分析方法,研究了四种神经免疫性疾病中海马的形状变形和相关认知缺陷。我们研究了 120 名患者(每组 30 名),包括多发性硬化症(MS)、视神经脊髓炎谱系障碍(NMOSD)、抗 NMDAR 和抗 LGI1 脑炎患者。每个患者样本都与来自 79 名健康参与者的池中的一个对照组相匹配。我们进行了基于 MRI 的顶点海马形状分析,提取了海马体积估计值和标量投影值作为表面位移的度量。认知测试包括对言语记忆和语义流畅性表现的评估。我们的横断面分析显示,MS、抗 NMDAR 脑炎和抗 LGI1 脑炎患者存在双侧向内变形的特征性模式,覆盖了海马表面的 32%,而 NMOSD 患者与对照组相比没有变形。主要在海马头部观察到显著的反转,伴随着体积损失,并与自身免疫性脑炎和 MS 中的语义流畅性评分和言语情景记忆相关。跨疾病的变形重叠分析显示,左侧前海马有一个汇聚区,与 CA1 亚区相对应。这个汇聚区表明免疫介导的损伤有一个共同的下游底物,似乎特别容易受到神经炎症过程的影响。我们的跨诊断形态学观点揭示了神经免疫性疾病中认知缺陷的相互病理生理途径,并激发了对海马对自身免疫易感性增加的机制的进一步研究。