Huntington's Disease Centre, Department of Neurodegenerative disease, UCL Queen Square Institute of Neurology, University College London, London, UK.
Centre for Medical Image Computing, Department of Computer Science, UCL, London, UK.
EBioMedicine. 2021 Mar;65:103266. doi: 10.1016/j.ebiom.2021.103266. Epub 2021 Mar 9.
Pathological processes in Huntington's disease (HD) begin many years prior to symptom onset. Recently we demonstrated that in a premanifest cohort approximately 24 years from predicted disease onset, despite intact function, there was evidence of subtle neurodegeneration. Here, we use novel imaging techniques to determine whether macro- and micro-structural changes can be detected across the whole-brain in the same cohort.
62 premanifest HD (PreHD) and 61 controls from the HD Young Adult Study (HD-YAS) were included. Grey and white matter volume, diffusion weighted imaging (DWI) measures of white matter microstructure, multiparametric maps (MPM) estimating myelin and iron content from magnetization transfer (MT), proton density (PD), longitudinal relaxation (R1) and effective transverse relaxation (R2*), and myelin g-ratio were examined. Group differences between PreHD and controls were assessed; associations between all imaging metrics and disease burden and CSF neurofilament light (NfL) were also performed. Volumetric and MPM results were corrected at a cluster-wise value of familywise error (FWE) 0.05. Diffusion and g-ratio results were corrected via threshold-free cluster enhancement at FWE 0.05.
We showed significantly increased R1 and R2*, suggestive of increased iron, in the putamen, globus pallidum and external capsule of PreHD participants. There was also a significant association between lower cortical R2*, suggestive of reduced myelin or iron, and higher CSF NfL in the frontal lobe and the parieto-occipital cortices. No other results were significant at corrected levels.
Increased iron in subcortical structures and the surrounding white matter is a feature of very early PreHD. Furthermore, increases in CSF NfL were linked to microstructural changes in the posterior parietal-occipital cortex, a region previously shown to undergo some of the earliest cortical changes in HD. These findings suggest that disease related process are occurring in both subcortical and cortical regions more than 20 years from predicted disease onset.
亨廷顿病(HD)的病理过程早在症状出现前多年就开始了。最近,我们发现在一个距预测发病时间还有 24 年的前驱期队列中,尽管功能完好,但仍有证据表明存在微妙的神经退行性变。在这里,我们使用新的成像技术来确定在同一队列中是否可以在整个大脑中检测到宏观和微观结构的变化。
本研究纳入了来自亨廷顿病青年研究(HD-YAS)的 62 名前驱期 HD(PreHD)患者和 61 名对照者。我们检查了灰质和白质体积、弥散加权成像(DWI)测量的白质微观结构、从磁化传递(MT)、质子密度(PD)、纵向弛豫(R1)和有效横向弛豫(R2*)估算髓鞘和铁含量的多参数图(MPM),以及髓鞘 g 比值。评估了 PreHD 和对照组之间的组间差异;还评估了所有成像指标与疾病负担和脑脊液神经丝轻链(NfL)之间的相关性。体积和 MPM 结果以家族错误(FWE)0.05 的聚类值进行校正。弥散和 g 比值结果通过 FWE 0.05 的无阈值聚类增强进行校正。
我们发现前驱期参与者的壳核、苍白球和外囊的 R1 和 R2增加,提示铁含量增加。额叶和顶枕叶皮质的 R2降低,提示髓鞘或铁含量减少,与 CSF NfL 呈显著正相关。在校正水平上,没有其他结果具有统计学意义。
皮质下结构和周围白质中铁含量的增加是非常早期 PreHD 的一个特征。此外,CSF NfL 的增加与顶枕叶后部皮质的微观结构变化有关,该区域先前被证明是 HD 中最早发生皮质变化的区域之一。这些发现表明,在预测发病时间 20 多年后,疾病相关过程不仅发生在皮质下区域,也发生在皮质区域。