Staging of progressive supranuclear palsy-Richardson syndrome using MRI brain charts for the human lifespan

被引:3
作者
Planche, Vincent [1 ,2 ,10 ]
Mansencal, Boris [3 ]
Manjon, Jose, V [4 ]
Meissner, Wassilios G. [1 ,5 ,6 ,7 ]
Tourdias, Thomas [8 ,9 ]
Coupe, Pierrick [3 ]
机构
[1] Univ Bordeaux, Inst Malad Neurodegenerat, CNRS, UMR 5293, F-33000 Bordeaux, France
[2] CHU Bordeaux, Ctr Memoire Ressources Rech, Serv Neurol Malad Neurodegenerat, Pole Neurosci Clin, F-33000 Bordeaux, France
[3] Univ Bordeaux, CNRS, UMR5800, Bordeaux INP,Lab Bordelais Rech Informat LaBRI, F-33400 Bordeaux, France
[4] Univ Politecn Valencia, Inst Aplicac Tecnol Informac & Comunicac Avanzadas, Camino Vera S-N, Valencia 46022, Spain
[5] CHU Bordeaux, Serv Neurol Malad Neurodegenerat, Reseau NS Pk FCRIN, F-33000 Bordeaux, France
[6] Dept Med, Christchurch, New Zealand
[7] New Zealand Brain Res Inst, Christchurch 8011, New Zealand
[8] Inserm U1215 Neuroctr Magendie, F-33000 Bordeaux, France
[9] CHU Bordeaux, Serv Neuroimagerie Diagnost & Therapeut, F-33000 Bordeaux, France
[10] Inst Malad Neurodegenerat, Ctr Broca Nouvelle Aquitaine, UMR CNRS 5293, 146 Rue Leo Saignat, F-33076 Bordeaux, France
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国工程与自然科学研究理事会; 美国国家卫生研究院; 加拿大健康研究院;
关键词
progressive supranuclear palsy; Richardson syndrome; MRI; brain charts; staging; ATROPHY; DIAGNOSIS; PSP;
D O I
10.1093/braincomms/fcae055
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Brain charts for the human lifespan have been recently proposed to build dynamic models of brain anatomy in normal aging and various neurological conditions. They offer new possibilities to quantify neuroanatomical changes from preclinical stages to death, where longitudinal MRI data are not available. In this study, we used brain charts to model the progression of brain atrophy in progressive supranuclear palsy-Richardson syndrome. We combined multiple datasets (n = 8170 quality controlled MRI of healthy subjects from 22 cohorts covering the entire lifespan, and n = 62 MRI of progressive supranuclear palsy-Richardson syndrome patients from the Four Repeat Tauopathy Neuroimaging Initiative (4RTNI)) to extrapolate lifetime volumetric models of healthy and progressive supranuclear palsy-Richardson syndrome brain structures. We then mapped in time and space the sequential divergence between healthy and progressive supranuclear palsy-Richardson syndrome charts. We found six major consecutive stages of atrophy progression: (i) ventral diencephalon (including subthalamic nuclei, substantia nigra, and red nuclei), (ii) pallidum, (iii) brainstem, striatum and amygdala, (iv) thalamus, (v) frontal lobe, and (vi) occipital lobe. The three structures with the most severe atrophy over time were the thalamus, followed by the pallidum and the brainstem. These results match the neuropathological staging of tauopathy progression in progressive supranuclear palsy-Richardson syndrome, where the pathology is supposed to start in the pallido-nigro-luysian system and spreads rostrally via the striatum and the amygdala to the cerebral cortex, and caudally to the brainstem. This study supports the use of brain charts for the human lifespan to study the progression of neurodegenerative diseases, especially in the absence of specific biomarkers as in PSP. Planche et al. combined multiple MRI datasets to extrapolate lifetime volumetric models for brain structures in healthy aging and progressive supranuclear palsy-Richardson syndrome. They proposed a descriptive MRI staging scheme for progressive supranuclear palsy-Richardson syndrome, comprising six major consecutive stages of atrophy progression that closely align with the neuropathological staging of tauopathy progression. Graphical abstract
引用
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页数:10
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