Mapping Neurodegenerative Disease Onset and Progression

被引:63
作者
Seeley, William W. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Memory & Aging Ctr, Dept Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Memory & Aging Ctr, Dept Pathol, San Francisco, CA 94143 USA
关键词
VARIANT FRONTOTEMPORAL DEMENTIA; INTRINSIC FUNCTIONAL CONNECTIVITY; HEXANUCLEOTIDE REPEAT EXPANSION; POSTERIOR CORTICAL ATROPHY; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; BRAIN CONNECTIVITY; DEFAULT-MODE; COGNITIVE IMPAIRMENT; NETWORK CONNECTIVITY;
D O I
10.1101/cshperspect.a023622
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Brain networks have been of long-standing interest to neurodegeneration researchers, including but not limited to investigators focusing on conventional prion diseases, which are known to propagate along neural pathways. Tools for human network mapping, however, remained inadequate, limiting our understanding of human brain network architecture and preventing clinical research applications. Until recently, neuropathological studies were the only viable approach to mapping disease onset and progression in humans but required large autopsy cohorts and laborious methods for whole-brain sectioning and staining. Despite important advantages, postmortem studies cannot address in vivo, physiological, or longitudinal questions and have limited potential to explore early-stage disease except for the most common disorders. Emerging in vivo network-based neuroimaging strategies have begun to address these issues, providing data that complement the neuropathological tradition. Overall, findings to date highlight several fundamental principles of neurodegenerative disease anatomy and pathogenesis, as well as some enduring mysteries. These principles and mysteries provide a road map for future research.
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页数:17
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