Insights into White Matter Damage in Alzheimer's Disease: From Postmortem to in vivo Diffusion Tensor MRI Studies

被引:48
作者
Caso, Francesca [1 ]
Agosta, Federica [1 ]
Filippi, Massimo [1 ,2 ]
机构
[1] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Neurosci, Inst Expt Neurol,Neuroimaging Res Unit, Via Olgettina 60, IT-20132 Milan, Italy
[2] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Neurosci, Inst Expt Neurol,Dept Neurol, Milan, Italy
关键词
Alzheimer's disease; White matter damage; Diffusion tensor magnetic resonance imaging; Tractography; Wallerian degeneration; Retrogenesis; Prion-like propagation; Neuroinflammation; MILD COGNITIVE IMPAIRMENT; CEREBRAL AMYLOID ANGIOPATHY; POSTERIOR CORTICAL ATROPHY; DEMENTIA; DEGENERATION; BRAIN; TRACT; TRACTOGRAPHY; DISRUPTION; MECHANISMS;
D O I
10.1159/000441422
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background: Alzheimer's disease (AD) has traditionally been considered a disease of the gray matter (GM). However, several pathological and neuroimaging studies provided evidence of white matter (WM) abnormalities in this disease. The advent of diffusion tensor (DT) MRI allowed researchers to study in vivo cerebral WM abnormalities in AD, including the earliest stage of the disease and its atypical variants. Objective: To provide a concise overview of the main neuropathological and DT MRI studies that explored WM damage in AD providing new insights into the underlying pathophysiological mechanisms. Results: Neuropathological studies revealed that GM and WM changes did not concur regionally in many areas, where well-preserved GM often lay over severely changed WM also in nondemented subjects with an underlying AD pathology. DT MRI studies confirmed in vivo a severe WM involvement in classical and atypical AD variants and in the prodromal stage of the disease. Microstructural WM damage was severer and more distributed than expected on the basis of cortical atrophy in all clinical AD phenotypes. Conclusions: AD is characterized by a relevant involvement of the WM as demonstrated by postmortem and in vivo evidence. WM microstructural damage in AD is not always secondary to neuronal loss, suggesting a role of other pathological mechanisms such as prion-like propagation of altered proteins or neuroinflammation. DT MRI offers new insight into AD pathophysiology and, more importantly, new possible targets for future experimental therapies. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:26 / 33
页数:8
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