Laansma Max A, Zhao Yuji, van Heese Eva M, Bright Joanna K, Owens-Walton Conor, Al-Bachari Sarah, Anderson Tim J, Assogna Francesca, van Balkom Tim D, Berendse Henk W, Cendes Fernando, Dalrymple-Alford John C, Debove Ines, Dirkx Michiel F, Druzgal Jason, Emsley Hedley C A, Fouche Jean-Paul, Garraux Gaëtan, Guimarães Rachel P, Helmich Rick C, Hu Michele, van den Heuvel Odile A, Isaev Dmitry, Kim Ho-Bin, Klein Johannes C, Lochner Christine, McMillan Corey T, Melzer Tracy R, Newman Benjamin, Parkes Laura M, Pellicano Clelia, Piras Fabrizio, Pitcher Toni L, Poston Kathleen L, Rango Mario, Ribeiro Leticia F, Rocha Cristiane S, Rummel Christian, Santos Lucas S R, Schmidt Reinhold, Schwingenschuh Petra, Squarcina Letizia, Stein Dan J, Vecchio Daniela, Vriend Chris, Wang Jiunjie, Weintraub Daniel, Wiest Roland, Yasuda Clarissa L, Jahanshad Neda, Thompson Paul M, van der Werf Ysbrand D, Gutman Boris A
Amsterdam UMC, Department of Anatomy and Neurosciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Amsterdam Neuroscience, Neurodegeneration, Amsterdam, The Netherlands.
NPJ Parkinsons Dis. 2024 Nov 19;10(1):223. doi: 10.1038/s41531-024-00825-9.
Alterations in subcortical brain regions are linked to motor and non-motor symptoms in Parkinson's disease (PD). However, associations between clinical expression and regional morphological abnormalities of the basal ganglia, thalamus, amygdala and hippocampus are not well established. We analyzed 3D T1-weighted brain MRI and clinical data from 2525 individuals with PD and 1326 controls from 22 global sources in the ENIGMA-PD consortium. We investigated disease effects using mass univariate and multivariate models on the medial thickness of 27,120 vertices of seven bilateral subcortical structures. Shape differences were observed across all Hoehn and Yahr (HY) stages, as well as correlations with motor and cognitive symptoms. Notably, we observed incrementally thinner putamen from HY1, caudate nucleus and amygdala from HY2, hippocampus, nucleus accumbens, and thalamus from HY3, and globus pallidus from HY4-5. Subregions of the thalami were thicker in HY1 and HY2. Largely congruent patterns were associated with a longer time since diagnosis and worse motor symptoms and cognitive performance. Multivariate regression revealed patterns predictive of disease stage. These cross-sectional findings provide new insights into PD subcortical degeneration by demonstrating patterns of disease stage-specific morphology, largely consistent with ongoing degeneration.
帕金森病(PD)患者大脑皮层下区域的改变与运动和非运动症状相关。然而,基底神经节、丘脑、杏仁核和海马体的临床症状与区域形态异常之间的关联尚未完全明确。我们分析了来自ENIGMA-PD联盟22个全球来源的2525名帕金森病患者和1326名对照者的3D T1加权脑MRI和临床数据。我们使用单变量和多变量模型研究了疾病对七个双侧皮层下结构的27120个顶点内侧厚度的影响。在所有Hoehn和Yahr(HY)分期中均观察到形状差异,以及与运动和认知症状的相关性。值得注意的是,我们观察到从HY1期开始壳核逐渐变薄,从HY2期开始尾状核和杏仁核变薄,从HY3期开始海马体、伏隔核和丘脑变薄,从HY4-5期开始苍白球变薄。丘脑亚区域在HY1和HY2期较厚。大体一致的模式与诊断后较长时间、更严重的运动症状和认知表现相关。多变量回归揭示了预测疾病分期的模式。这些横断面研究结果通过展示疾病分期特异性形态模式,为帕金森病皮层下变性提供了新的见解,这在很大程度上与正在进行的变性一致。