Neuropsychiatry, Royal Melbourne Hospital, Parkville, Victoria, Australia.
Melbourne Neuropsychiatry Center, University of Melbourne, Parkville, Victoria, Australia.
Eur J Neurol. 2023 Sep;30(9):2650-2660. doi: 10.1111/ene.15918. Epub 2023 Jun 23.
While individuals with Huntington disease (HD) show memory impairment that indicates hippocampal dysfunction, the available literature does not consistently identify structural evidence for involvement of the whole hippocampus but rather suggests that hippocampal atrophy may be confined to certain hippocampal subregions.
We processed T1-weighted MRI from IMAGE-HD study using FreeSurfer 7.0 and compared the volumes of the hippocampal subfields among 36 early motor symptomatic (symp-HD), 40 pre-symptomatic (pre-HD), and 36 healthy control individuals across three timepoints over 36 months.
Mixed-model analyses revealed significantly lower subfield volumes in symp-HD, compared with pre-HD and control groups, in the subicular regions of the perforant-pathway: presubiculum, subiculum, dentate gyrus, tail, and right molecular layer. These adjoining subfields aggregated into a single principal component, which demonstrated an accelerated rate of atrophy in the symp-HD. Volumes between pre-HD and controls did not show any significant difference. In the combined HD groups, CAG repeat length and disease burden score were associated with presubiculum, molecular layer, tail, and perforant-pathway subfield volumes. Hippocampal left tail and perforant-pathway subfields were associated with motor onset in the pre-HD group.
Hippocampal subfields atrophy in early symptomatic HD affects key regions of the perforant-pathway, which may implicate the distinctive memory impairment at this stage of illness. Their volumetric associations with genetic and clinical markers suggest the selective susceptibility of these subfields to mutant Huntingtin and disease progression.
虽然亨廷顿病(HD)患者表现出记忆障碍,表明海马功能障碍,但现有文献并未一致确定整个海马体的结构证据,而是表明海马体萎缩可能局限于某些海马体亚区。
我们使用 FreeSurfer 7.0 处理了 IMAGE-HD 研究中的 T1 加权 MRI,并在 36 名早期运动症状(symp-HD)、40 名无症状前(pre-HD)和 36 名健康对照个体中比较了 36 个月内三个时间点的海马亚区体积。
混合模型分析显示,与 pre-HD 和对照组相比,symp-HD 的海马亚区体积明显较低,在穿通通路的海马亚区:内嗅皮质、海马体、齿状回、尾状核和右侧分子层。这些相邻的亚区聚集为一个单独的主成分,表明 symp-HD 的萎缩速度加快。pre-HD 和对照组之间的体积没有显示出任何显著差异。在合并的 HD 组中,CAG 重复长度和疾病负担评分与 presubiculum、分子层、尾状核和穿通通路亚区体积相关。在 pre-HD 组中,海马体左侧尾部和穿通通路亚区与运动起始相关。
早期症状性 HD 的海马体亚区萎缩影响了穿通通路的关键区域,这可能暗示了在疾病的这个阶段特有的记忆障碍。它们与遗传和临床标志物的体积相关性表明,这些亚区对突变亨廷顿蛋白和疾病进展具有选择性易感性。