Dementia in Down's syndrome

被引:160
|
作者
Ballard, Clive [1 ]
Mobley, William [2 ]
Hardy, John [3 ]
Williams, Gareth [1 ]
Corbett, Anne [1 ]
机构
[1] Kings Coll London, Wolfson Ctr Age Related Dis, London SE1 1UL, England
[2] Univ Calif San Diego, Sch Med, Ctr Neural Circuits & Behav, San Diego, CA 92103 USA
[3] UCL, Dept Mol Neurosci, London, England
来源
LANCET NEUROLOGY | 2016年 / 15卷 / 06期
基金
美国国家卫生研究院;
关键词
TS65DN MOUSE MODEL; ALZHEIMER-TYPE DEMENTIA; APOLIPOPROTEIN-E; AMYLOID-BETA; GENE-EXPRESSION; A-BETA; COGNITIVE IMPAIRMENT; MOLECULAR-MECHANISMS; APP DUPLICATION; BINDING PROTEIN;
D O I
10.1016/S1474-4422(16)00063-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Down's syndrome is the most common genetic cause of learning difficulties, and individuals with this condition represent the largest group of people with dementia under the age of 50 years. Genetic drivers result in a high frequency of Alzheimer's pathology in these individuals, evident from neuroimaging, biomarker, and neuropathological findings, and a high incidence of cognitive decline and dementia. However, cognitive assessment is challenging, and diagnostic methods have not been fully validated for use in these patients; hence, early diagnosis remains difficult. Evidence regarding the benefits of cholinesterase inhibitors and other therapeutic options to treat or delay progressive cognitive decline or dementia is very scarce. Despite close similarities with late-onset Alzheimer's disease, individuals with Down's syndrome respond differently to treatment, and a targeted approach to drug development is thus necessary. Genetic and preclinical studies off er opportunities for treatment development, and potential therapies have been identified using these approaches.
引用
收藏
页码:622 / 636
页数:15
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