Brain connectivity in neurodegenerative diseases-from phenotype to proteinopathy

被引:236
作者
Pievani, Michela [1 ]
Filippini, Nicola [2 ]
van den Heuvel, Martijn P. [3 ]
Cappa, Stefano F. [4 ]
Frisoni, Giovanni B. [5 ,6 ,7 ]
机构
[1] Ist Ctr San Giovanni Dio, Lab Epidemiol Neuroimaging & Telemed LENITEM, I-25125 Brescia, Italy
[2] Warneford Hosp, Univ Dept Psychiat, Oxford OX3 7JX, England
[3] Univ Med Ctr, Brain Ctr Rudolf Magnus, NL-3908 GA Utrecht, Netherlands
[4] IUSS, I-27100 Pavia, Italy
[5] Univ Hosp, Memory Clin, CH-1225 Geneva, Switzerland
[6] Univ Hosp, LANVIE Lab Neuroimaging Aging, CH-1225 Geneva, Switzerland
[7] Univ Geneva, CH-1225 Geneva, Switzerland
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; RESTING-STATE NETWORKS; RICH-CLUB ORGANIZATION; WHITE-MATTER INTEGRITY; CORTICO-STRIATAL CONNECTIVITY; MILD COGNITIVE IMPAIRMENT; EARLY HUNTINGTONS-DISEASE; VOXEL-BASED MORPHOMETRY; FUNCTIONAL CONNECTIVITY; DIFFUSION TENSOR;
D O I
10.1038/nrneurol.2014.178
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Functional and structural connectivity measures, as assessed by means of functional and diffusion MRI, are emerging as potential intermediate biomarkers for Alzheimer disease (AD) and other disorders. This Review aims to summarize current evidence that connectivity biomarkers are associated with upstream and downstream disease processes (molecular pathology and clinical symptoms, respectively) in the major neurodegenerative diseases. The vast majority of studies have addressed functional and structural connectivity correlates of clinical phenotypes, confirming the predictable correlation with topography and disease severity in AD and frontotemporal dementia. In neurodegenerative diseases with motor symptoms, structural-but, to date, not functional-connectivity has been consistently found to be associated with clinical phenotype and disease severity. In the latest studies, the focus has moved towards the investigation of connectivity correlates of molecular pathology. Studies in cognitively healthy individuals with brain amyloidosis or genetic risk factors for AD have shown functional connectivity abnormalities in preclinical disease stages that are reminiscent of abnormalities observed in symptomatic AD. This shift in approach is promising, and may aid identification of early disease markers, establish a paradigm for other neurodegenerative disorders, shed light on the molecular neurobiology of connectivity disruption and, ultimately, clarify the pathophysiology of neurodegenerative diseases.
引用
收藏
页码:620 / 633
页数:14
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