Max Planck Institute for Human Cognitive and Brain Sciences Leipzig, Germany.
Max Planck Institute for Human Cognitive and Brain Sciences Leipzig, Germany; Department of Medical Engineering and Biotechnology, University of Applied Science, Jena, Germany; Leipzig University Medical Center, IFB Adiposity Diseases, Germany.
Neuroimage Clin. 2019;22:101722. doi: 10.1016/j.nicl.2019.101722. Epub 2019 Feb 19.
Progressive supranuclear palsy (PSP) is an atypical parkinsonian syndrome characterized by vertical gaze palsy and postural instability. Midbrain atrophy is suggested as a hallmark, but it has not been validated systematically in whole-brain imaging.
We conducted whole-brain meta-analyses identifying disease-related atrophy in structural MRI. Eighteen studies were identified (N = 315 PSP, 393 controls) and separated into gray or white matter analyses (15/12). All patients were diagnosed according to the National Institute of Neurological Disorders and Stroke and the Society for PSP (NINDS-SPSP criteria, Litvan et al. (1996a)), which are now considered as PSP-Richardson syndrome (Höglinger et al., 2017). With overlay analyses, we double-validated two meta-analytical algorithms: anatomical likelihood estimation and seed-based D mapping. Additionally, we conducted region-of-interest effect size meta-analyses on radiological biomarkers and subtraction analyses differentiating PSP from Parkinson's disease.
Whole brain meta-analyses revealed consistent gray matter atrophy in bilateral thalamus, anterior insulae, midbrain, and left caudate nucleus. White matter alterations were consistently detected in bilateral superior/middle cerebellar pedunculi, cerebral pedunculi, and midbrain atrophy. Region-of-interest meta-analyses demonstrated that midbrain metrics generally perform very well in distinguishing PSP from other parkinsonian syndromes with strong effect sizes. Subtraction analyses identified the midbrain as differentiating between PSP and Parkinson's disease.
Our meta-analyses identify gray matter atrophy of the midbrain and white matter atrophy of the cerebral/cerebellar pedunculi and midbrain as characteristic for PSP. Results support the incorporation of structural MRI data, and particularly these structures, into the revised PSP diagnostic criteria.
进行性核上性麻痹(PSP)是一种非典型的帕金森综合征,其特征为垂直性眼球运动障碍和姿势不稳。中脑萎缩被认为是其标志,但在全脑成像中尚未得到系统验证。
我们进行了全脑荟萃分析,以确定结构 MRI 中的疾病相关萎缩。共确定了 18 项研究(PSP 患者 315 例,对照组 393 例),并分为灰质或白质分析(15/12)。所有患者均根据国立神经病学与卒中研究所和 PSP 协会(NINDS-SPSP 标准,Litvan 等人,1996a)进行诊断,现在被认为是 PSP-Richardson 综合征(Höglinger 等人,2017)。通过叠加分析,我们双重验证了两种荟萃分析算法:解剖似然估计和基于种子的 D 映射。此外,我们还对放射学生物标志物进行了感兴趣区效应量荟萃分析,并进行了区分 PSP 和帕金森病的减影分析。
全脑荟萃分析显示双侧丘脑、前岛叶、中脑和左侧尾状核存在一致的灰质萎缩。在双侧小脑上/中脑脚、大脑脚和中脑萎缩中一致检测到白质改变。感兴趣区荟萃分析表明,中脑指标通常在区分 PSP 与其他帕金森综合征方面表现非常出色,具有很强的效应量。减影分析确定中脑可区分 PSP 和帕金森病。
我们的荟萃分析确定中脑灰质萎缩和大脑/小脑脚及中脑白质萎缩是 PSP 的特征。结果支持将结构 MRI 数据,特别是这些结构,纳入修订后的 PSP 诊断标准。