Graph Models of Pathology Spread in Alzheimer's Disease: An Alternative to Conventional Graph Theoretic Analysis

被引:13
作者
Raj, Ashish [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 1 Irving St,Suite AC116, San Francisco, CA 94122 USA
关键词
Alzheimer's disease; amyloid beta; graph theory; network diffusion; protein aggregation; tau; trans-neuronal spread; WHITE-MATTER INTEGRITY; FRONTOTEMPORAL LOBAR DEGENERATION; STATE FUNCTIONAL CONNECTIVITY; NETWORK DIFFUSION-MODEL; SYNTHETIC TAU FIBRILS; NEURODEGENERATIVE DISEASES; IN-VIVO; A-BETA; NEUROFIBRILLARY TANGLES; NEURONAL VULNERABILITY;
D O I
10.1089/brain.2020.0905
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Graph theory and connectomics are new techniques for uncovering disease-induced changes in the brain's structural network. Most prior studied have focused on network statistics as biomarkers of disease. However, an emerging body of work involves exploring how the network serves as a conduit for the propagation of disease factors in the brain and has successfully mapped the functional and pathological consequences of disease propagation. In Alzheimer' s disease (AD), progressive deposition of misfolded proteins amyloid and tau is wellknown to follow fiber projections, under a "prion-like" trans-neuronal transmission mechanism, through which misfolded proteins cascade along neuronal pathways, giving rise to network spread. Methods: In this review, we survey the state of the art in mathematical modeling of connectome-mediated pathology spread in AD. Then we address several open questions that are amenable to mathematically precise parsimonious modeling of pathophysiological processes, extrapolated to the whole brain. We specifically identify current formal models of how misfolded proteins are produced, aggregate, and disseminate in brain circuits, and attempt to understand how this process leads to stereotyped progression in Alzheimer's and other related diseases. Conclusion: This review serves to unify current efforts in modeling of AD progression that together have the potential to explain observed phenomena and serve as a test-bed for future hypothesis generation and testing in silico.
引用
收藏
页码:799 / 814
页数:16
相关论文
共 206 条
[61]   Propagation of Tau Misfolding from the Outside to the Inside of a Cell [J].
Frost, Bess ;
Jacks, Rachel L. ;
Diamond, Marc I. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (19) :12845-12852
[62]   Conformational Diversity of Wild-type Tau Fibrils Specified by Templated Conformation Change [J].
Frost, Bess ;
Ollesch, Julian ;
Wille, Holger ;
Diamond, Marc I. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (06) :3546-3551
[63]  
Fusco FR, 1999, J NEUROSCI, V19, P1189
[64]   Dipy, a library for the analysis of diffusion MRI data [J].
Garyfallidis, Eleftherios ;
Brett, Matthew ;
Amirbekian, Bagrat ;
Rokem, Ariel ;
van der Walt, Stefan ;
Descoteaux, Maxime ;
Nimmo-Smith, Ian .
FRONTIERS IN NEUROINFORMATICS, 2014, 8
[65]   Formation and propagation of tau oligomeric seeds [J].
Gerson, Julia E. ;
Kayed, Rakez .
FRONTIERS IN NEUROLOGY, 2013, 4
[66]   Modelling amyloid fibril formation kinetics: mechanisms of nucleation and growth [J].
Gillam, J. E. ;
MacPhee, C. E. .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2013, 25 (37)
[67]   The minimal preprocessing pipelines for the Human Connectome Project [J].
Glasser, Matthew F. ;
Sotiropoulos, Stamatios N. ;
Wilson, J. Anthony ;
Coalson, Timothy S. ;
Fischl, Bruce ;
Andersson, Jesper L. ;
Xu, Junqian ;
Jbabdi, Saad ;
Webster, Matthew ;
Polimeni, Jonathan R. ;
Van Essen, David C. ;
Jenkinson, Mark .
NEUROIMAGE, 2013, 80 :105-124
[68]   Reduced glucose uptake and Aβ in brain regions with hyperintensities in connected white matter [J].
Glodzik, L. ;
Kuceyeski, A. ;
Rusinek, H. ;
Tsui, W. ;
Mosconi, L. ;
Li, Y. ;
Osorio, R. S. ;
Williams, S. ;
Randall, C. ;
Spector, N. ;
McHugh, P. ;
Murray, J. ;
Pirraglia, E. ;
Vallabhajosula, S. ;
Raj, A. ;
de Leon, M. J. .
NEUROIMAGE, 2014, 100 :684-691
[69]   Alterations in multiple measures of white matter integrity in normal women at high risk for Alzheimer's disease [J].
Gold, Brian T. ;
Powell, David K. ;
Andersen, Anders H. ;
Smith, Charles D. .
NEUROIMAGE, 2010, 52 (04) :1487-1494
[70]   Cognition and anatomy in three variants of primary progressive aphasia [J].
Gorno-Tempini, ML ;
Dronkers, NF ;
Rankin, KP ;
Ogar, JM ;
Phengrasamy, L ;
Rosen, HJ ;
Johnson, JK ;
Weiner, MW ;
Miller, BL .
ANNALS OF NEUROLOGY, 2004, 55 (03) :335-346