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Morphological alterations in the caudate putamen pallidum and thalamus in Parkinsons disease

机译:帕金森氏病的尾状壳状苍白质和丘脑形态学改变

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摘要

Like many neurodegenerative diseases, the clinical symptoms of Parkinsons disease (PD) do not manifest until significant progression of the disease has already taken place, motivating the need for sensitive biomarkers of the disease. While structural imaging is a potentially attractive method due to its widespread availability and non-invasive nature, global morphometric measures (e.g., volume) have proven insensitive to subtle disease change. Here we use individual surface displacements from deformations of an average surface model to capture disease related changes in shape of the subcortical structures in PD. Data were obtained from both the University of British Columbia (UBC) [n = 54 healthy controls (HC) and n = 55 Parkinsons disease (PD) patients] and the publicly available Parkinsons Progression Markers Initiative (PPMI) [n = 137 (HC) and n = 189 (PD)] database. A high dimensional non-rigid registration algorithm was used to register target segmentation labels (caudate, putamen, pallidum, and thalamus) to a set of segmentation labels defined on the average-template. The vertex-wise surface displacements were significantly different between PD and HC in thalamic and caudate structures. However, overall displacements did not correlate with disease severity, as assessed by the Unified Parkinson's Disease Rating Scale (UPDRS). The results from this study suggest disease-relevant shape abnormalities can be robustly detected in subcortical structures in PD. Future studies will be required to determine if shape changes in subcortical structures are seen in the prodromal phases of the disease.
机译:像许多神经退行性疾病一样,帕金森氏病(PD)的临床症状要等到该病的明显进展才显现出来,从而激发了对该病敏感的生物标志物的需求。尽管结构成像由于其广泛的可用性和非侵入性的性质而成为一种潜在的有吸引力的方法,但是已证明整体形态测量(例如体积)对细微的疾病变化不敏感。在这里,我们使用来自平均表面模型变形的单个表面位移来捕获与疾病相关的PD皮质下结构形状的变化。数据来自不列颠哥伦比亚大学(UBC)[n = 54名健康对照(HC)和n = 55名帕金森病(PD)患者]和公开可用的帕金森病进展标记倡议(PPMI)[n = 137(HC )和n = 189(PD)]数据库。高维非刚性配准算法用于将目标细分标签(尾状,壳壳,苍白球和丘脑)注册到在平均模板上定义的一组细分标签中。丘脑和尾状结构中PD和HC之间的顶点方向表面位移明显不同。但是,根据统一帕金森氏疾病评分量表(UPDRS)评估,总体移位与疾病严重程度无关。这项研究的结果表明,可以在PD的皮层下结构中可靠地检测出与疾病相关的形状异常。将需要进一步的研究来确定在疾病的前驱期是否可见皮质下结构的形状变化。

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