E08 Tracking the neurodegeneration pattern of the anterior thalamic radiations in HD: a focus on brain iron, white matter integrity and metabolites

M. D. Ayllón, C. García-Gorro, S. Martínez-Horta, J. Pérez-Pérez, J. Kulisevsky, N. Rodríguez-Dechicha, I. Vaquer, S. Subirà, M. Calopa, E. Muñoz, P. Santacruz, Jesús Ruiz-Idiago, C. Mareca, R. D. Diego-Balaguer, E. Càmara
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Abstract

Background HD is a suitable model to monitor the whole neurodegeneration process. Huntington’s disease (HD) affects primarily the striatum, but loss of white matter (WM) integrity and iron homeostasis disruption have been also described. These anomalies together with metabolite profiles could unveil the pathophysiologic mechanisms involved. Aims To assess the temporal and spatial progression of neurodegeneration on both anterior thalamic radiations (ATR). Methods Thirty-one HD gene carriers and twenty-four controls underwent neuropsychological evaluation and were scanned at 3T-MRI unit. A multimodal study was conducted to measure relaxometry, diffusivity and spectroscopy as proxies of iron, WM microstructure and metabolite composition, respectively. Three statistical approaches (average, segmental, along-the-tract) were performed, with MANOVA and post-hoc Tukey test to evaluate differences among groups and Pearson test to assess correlations. Results ATR disintegration began in premanifest individuals and progressed in extent and severity in manifest patients. WM damage was more extensive in the right ATR that could translate a higher vulnerability and showed a spatial gradient from subcortical to deep WM in favour of the dying-back hypothesis. Iron was increased in the left ATR in premanifest individuals that might uncover a dysregulated myelination or an abnormal ferritin accumulation. NAA and creatine decreased exclusively in manifest patients suggesting neuronal loss and mitochondrial dysfunction. Furthermore, imaging parameters could be used as biomarkers given their links with clinical scores. Conclusions The complex neurodegeneration pattern of ATR in HD can help to understand the pathophysiological mechanisms underlying HD progression. The multimodal approach and along-the-tract analysis allow for a more comprehensive evaluation of neurodegeneration.
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追踪HD前丘脑辐射的神经退行性变模式:关注脑铁、白质完整性和代谢物
HD是一种适合监测整个神经退行性变过程的模型。亨廷顿氏病(HD)主要影响纹状体,但白质(WM)完整性丧失和铁稳态破坏也有报道。这些异常与代谢物谱可以揭示所涉及的病理生理机制。目的探讨丘脑前辐射(ATR)对神经退行性变的时空影响。方法对31例HD基因携带者和24例对照者进行神经心理评估,并进行3T-MRI扫描。一项多模式研究分别测量了作为铁、WM微观结构和代谢物组成代表的弛豫测量、扩散系数和光谱。采用三种统计方法(平均、分段、沿道),采用方差分析和事后Tukey检验评估组间差异,Pearson检验评估相关性。结果ATR解体开始于未出现症状的个体,在出现症状的患者中其程度和严重程度均有进展。右侧ATR的WM损伤更广泛,这可以转化为更高的脆弱性,并显示出从皮质下到深部WM的空间梯度,这有利于死背假说。铁在预显个体的左ATR中增加,这可能揭示髓鞘形成失调或铁蛋白积累异常。NAA和肌酸仅在显性患者中下降,提示神经元丢失和线粒体功能障碍。此外,鉴于成像参数与临床评分的联系,它们可以用作生物标志物。结论HD患者ATR复杂的神经退行性变模式有助于了解HD进展的病理生理机制。多模态方法和沿道分析允许对神经变性进行更全面的评估。
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