Connectome-based modelling of neurodegenerative diseases: towards precision medicine and mechanistic insight

被引:43
|
作者
Vogel, Jacob W. [1 ]
Corriveau-Lecavalier, Nick [2 ,3 ]
Franzmeier, Nicolai [4 ,5 ,6 ]
Pereira, Joana B. [7 ,8 ]
Brown, Jesse A. [9 ]
Maass, Anne [10 ]
Botha, Hugo [2 ]
Seeley, William W. [9 ,11 ]
Bassett, Dani S. [12 ,13 ,14 ,15 ,16 ]
Jones, David T. [2 ,17 ]
Ewers, Michael [4 ]
机构
[1] Lund Univ, Dept Clin Sci, SciLifeLab, Lund, Sweden
[2] Mayo Clin, Dept Neurol, Rochester, MN USA
[3] Mayo Clin, Dept Psychiat & Psychol, Rochester, MN USA
[4] Ludwig Maximilians Univ Munchen, Univ Hosp, Inst Stroke & Dementia Res ISD, Munich, Germany
[5] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[6] Univ Gothenburg, Sahlgrenska Acadamy, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Gothenburg, Sweden
[7] Lund Univ, Dept Clin Sci, Clin Memory Res Unit, Malmo, Sweden
[8] Karolinska Inst, Dept Clin Neurosci, Neuro Div, Stockholm, Sweden
[9] Univ Calif San Francisco, Memory & Aging Ctr, Dept Neurol, San Francisco, CA USA
[10] German Ctr Neurodegenerat Dis DZNE, Magdeburg, Germany
[11] Univ Calif San Francisco, Dept Pathol, San Francisco, CA USA
[12] Univ Penn, Dept Bioengn, Philadelphia, PA USA
[13] Univ Penn, Dept Elect & Syst Engn Phys & Astron, Philadelphia, PA USA
[14] Univ Penn, Dept Phys & Astron, Philadelphia, PA USA
[15] Univ Penn, Dept Neurol & Psychiat, Philadelphia, PA USA
[16] Santa Fe Inst, Santa Fe, NM 87501 USA
[17] Mayo Clin, Dept Radiol, Rochester, MN USA
关键词
MILD COGNITIVE IMPAIRMENT; VARIANT FRONTOTEMPORAL DEMENTIA; STATE FUNCTIONAL CONNECTIVITY; CASCADING NETWORK FAILURE; AMYLOID-BETA DEPOSITION; ALZHEIMERS-DISEASE; TAU PATHOLOGY; BEHAVIORAL VARIANT; MOUSE MODEL; HIPPOCAMPAL HYPERACTIVATION;
D O I
10.1038/s41583-023-00731-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurodegenerative diseases are the most common cause of dementia. Although their underlying molecular pathologies have been identified, there is substantial heterogeneity in the patterns of progressive brain alterations across and within these diseases. Recent advances in neuroimaging methods have revealed that pathological proteins accumulate along specific macroscale brain networks, implicating the network architecture of the brain in the system-level pathophysiology of neurodegenerative diseases. However, the extent to which 'network-based neurodegeneration' applies across the wide range of neurodegenerative disorders remains unclear. Here, we discuss the state-of-the-art of neuroimaging-based connectomics for the mapping and prediction of neurodegenerative processes. We review findings supporting brain networks as passive conduits through which pathological proteins spread. As an alternative view, we also discuss complementary work suggesting that network alterations actively modulate the spreading of pathological proteins between connected brain regions. We conclude this Perspective by proposing an integrative framework in which connectome-based models can be advanced along three dimensions of innovation: incorporating parameters that modulate propagation behaviour on the basis of measurable biological features; building patient-tailored models that use individual-level information and allowing model parameters to interact dynamically over time. We discuss promises and pitfalls of these strategies for improving disease insights and moving towards precision medicine. Neurodegenerative diseases show idiosyncratic spatial patterns of progressive protein malformations in the brain. In this Perspective, Vogel et al. discuss the role of inter-regional connectivity in constraining and modulating the spread of pathological proteins and provide a framework for patient-tailored prognostics.
引用
收藏
页码:620 / 639
页数:20
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