Focal temporal pole atrophy and network degeneration in semantic variant primary progressive aphasia

被引:89
作者
Collins, Jessica A. [1 ,6 ]
Montal, Victor [2 ]
Hochberg, Daisy [1 ]
Quimby, Megan [1 ]
Mandelli, Maria Luisa [3 ]
Makris, Nikos [4 ]
Seeley, William W. [3 ,5 ]
Gorno-Tempini, Maria Luisa [3 ]
Dickerson, Bradford C. [1 ,6 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA USA
[2] Univ Autonoma Barcelona, Hosp St Pau, Inst Invest Biomed St Pau, Dept Neurol, Barcelona, Spain
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[4] Harvard Med Sch, Massachusetts Gen Hosp, Dept Psychiat, Charlestown, MA USA
[5] Univ Calif San Francisco, Dept Pathol, San Francisco, CA USA
[6] MGH Frontotemporal Disorders Unit, 149 13th St, Charlestown, MA 02129 USA
基金
美国国家卫生研究院;
关键词
atrophy; resting state connectivity; primary progressive aphasia; semantic dementia; temporal lobe; MIDDLE LONGITUDINAL FASCICLE; INTRINSIC FUNCTIONAL CONNECTIVITY; SURFACE-BASED ANALYSIS; WHITE-MATTER; ALZHEIMERS-DISEASE; RESTING-STATE; LOBE ATROPHY; IN-VIVO; FRONTOTEMPORAL DEMENTIA; STRUCTURAL CONNECTIVITY;
D O I
10.1093/brain/aww313
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There are conflicting data on the origin and progression of neurodegeneration in semantic variant primary progressive aphasia (svPPA). Collins et al. identify a left temporal pole region with consistent atrophy in two patient cohorts. The region's connectivity in healthy adults predicts the localization and magnitude of distributed atrophy in svPPA. A wealth of neuroimaging research has associated semantic variant primary progressive aphasia with distributed cortical atrophy that is most prominent in the left anterior temporal cortex; however, there is little consensus regarding which region within the anterior temporal cortex is most prominently damaged, which may indicate the putative origin of neurodegeneration. In this study, we localized the most prominent and consistent region of atrophy in semantic variant primary progressive aphasia using cortical thickness analysis in two independent patient samples (n = 16 and 28, respectively) relative to age-matched controls (n = 30). Across both samples the point of maximal atrophy was located in the same region of the left temporal pole. This same region was the point of maximal atrophy in 100% of individual patients in both semantic variant primary progressive aphasia samples. Using resting state functional connectivity in healthy young adults (n = 89), we showed that the seed region derived from the semantic variant primary progressive aphasia analysis was strongly connected with a large-scale network that closely resembled the distributed atrophy pattern in semantic variant primary progressive aphasia. In both patient samples, the magnitude of atrophy within a brain region was predicted by that region's strength of functional connectivity to the temporopolar seed region in healthy adults. These findings suggest that cortical atrophy in semantic variant primary progressive aphasia may follow connectional pathways within a large-scale network that converges on the temporal pole.
引用
收藏
页码:457 / 471
页数:15
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