Is synaptic loss a unique hallmark of Alzheimer's disease?

被引:98
作者
Scheff, Stephen W. [1 ,2 ,3 ]
Neltner, Janna H. [4 ,5 ]
Nelson, Peter T. [2 ,3 ,4 ,5 ]
机构
[1] Univ Kentucky, Med Ctr, Dept Anat & Neurobiol, Lexington, KY 40536 USA
[2] Univ Kentucky, Med Ctr, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
[3] Univ Kentucky, Med Ctr, Alzheimers Dis Ctr, Lexington, KY 40536 USA
[4] Univ Kentucky, Med Ctr, Dept Pathol, Lexington, KY 40536 USA
[5] Univ Kentucky, Med Ctr, Div Neuropathol, Lexington, KY 40536 USA
基金
美国国家卫生研究院;
关键词
TDP-43; Neuropathology; Cerebrovascular; Hippocampal sclerosis; HS-Aging; MILD COGNITIVE IMPAIRMENT; FRONTOTEMPORAL LOBAR DEGENERATION; PROGRESSIVE SUPRANUCLEAR PALSY; LEWY BODY DISEASE; CEREBRAL GREY-MATTER; HIPPOCAMPAL SCLEROSIS; NEUROFIBRILLARY TANGLES; TAU-PROTEIN; NEUROPATHOLOGIC ASSESSMENT; QUANTITATIVE ASSESSMENT;
D O I
10.1016/j.bcp.2013.12.028
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Synapses may represent a key nidus for dementia including Alzheimer's disease (AD) pathogenesis. Here we review published studies and present new ideas related to the question of the specificity of synapse loss in AD. Currently, AD is defined by the regional presence of neuritic plaques and neurofibrillary tangles in the brain. The severity of involvement by those pathological hallmarks tends to correlate both with antemortem cognitive status, and also with synapse loss in multiple brain areas. Recent studies from large autopsy series have led to a new standard of excellence with regard to clinical-pathological correlation and to improved comprehension of the numerous brain diseases of the elderly. These studies have provided evidence that it is the rule rather than the exception for brains of aged individuals to demonstrate pathologies (often multiple) other than AD plaques and tangles. For many of these comorbid pathologies, the extent of synapse loss is imperfectly understood but could be substantial. These findings indicate that synapse loss is probably not a hallmark specific to AD but rather a change common to many diseases associated with dementia. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:517 / 528
页数:12
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