Cerebrovascular pathology in Down syndrome and Alzheimer disease

被引:56
|
作者
Head, Elizabeth [1 ]
Phelan, Michael J. [2 ]
Doran, Eric [3 ]
Kim, Ronald C. [4 ]
Poon, Wayne W. [5 ]
Schmitt, Frederick A. [1 ,7 ]
Lott, Ira T. [3 ,6 ]
机构
[1] Univ Kentucky, Sanders Brown Ctr Aging, 800 South Limestone St, Lexington, KY 40536 USA
[2] Univ Calif Irvine, Dept Stat, Irvine, CA USA
[3] Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
[4] Univ Calif Irvine, Dept Pathol, Irvine, CA 92717 USA
[5] Univ Calif Irvine, Inst Memory Impairments & Neurol Disorders, Irvine, CA USA
[6] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[7] Univ Kentucky, Dept Neurol, Lexington, KY 40536 USA
来源
基金
美国国家卫生研究院;
关键词
Arteriolosclerosis; Atherosclerosis; Cerebral amyloid angiopathy; Trisomy; 21; Vascular risk factors; CEREBRAL AMYLOID ANGIOPATHY; VASCULAR COGNITIVE IMPAIRMENT; RISK-FACTORS; DEMENTIA; HEMORRHAGE; NEUROPATHOLOGY; BRAINS; ADULTS; ATHEROSCLEROSIS; ASSOCIATION;
D O I
10.1186/s40478-017-0499-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD) with age. Typically, by age 40 years, most people with DS have sufficient neuropathology for an AD diagnosis. Interestingly, atherosclerosis and hypertension are atypical in DS with age, suggesting the lack of these vascular risk factors may be associated with reduced cerebrovascular pathology. However, because the extra copy of APP leads to increased beta-amyloid peptide (A beta) accumulation in DS, we hypothesized that there would be more extensive and widespread cerebral amyloid angiopathy (CAA) with age in DS relative to sporadic AD. To test this hypothesis CAA, atherosclerosis and arteriolosclerosis were used as measures of cerebrovascular pathology and compared in post mortem tissue from individuals with DS (n = 32), sporadic AD (n = 80) and controls (n = 37). CAA was observed with significantly higher frequencies in brains of individuals with DS compared to sporadic AD and controls. Atherosclerosis and arteriolosclerosis were rare in the cases with DS. CAA in DS may be a target for future interventional clinical trials.
引用
收藏
页数:9
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