唐氏综合症中的阿尔茨海默病。

Elizabeth Head, David Powell, Brian T Gold, Frederick A Schmitt
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摘要

随着年龄的增长,患有唐氏综合症(DS)的成年人面临的一个关键挑战是认知能力下降、痴呆和阿尔茨海默病(AD)的风险增加。在40-49岁的DS患者中,5.7-55%可能出现临床痴呆,而在50-59岁之间,痴呆患病率为4-55%(文献回顾[1])。尽管对痴呆患病率的报道范围很广,但退行性痴呆患者衰老的一个一致特征是AD脑病理的渐进式积累。到40岁时,几乎所有患者都有足够的老年斑和神经原纤维缠结,可用于AD的神经病理学诊断[2]。因此,阿尔茨海默病神经病理发病年龄(40岁)与临床痴呆症状增加之间存在分离。我们讨论了额叶损伤是影响认知功能的关键因素,并与白质(WM)和AD神经病理有关的假设。虽然这些可能是转化为痴呆的早期迹象,但我们也回顾了其他几种可能导致痴呆发病的临床合并症。
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Alzheimer's Disease in Down Syndrome.

A key challenge to adults with Down syndrome (DS) as they age is an increased risk for cognitive decline, dementia, and Alzheimer disease (AD). In DS persons ranging from 40-49 years of age, 5.7-55% may be clinically demented and between 50-59 years, dementia prevalence ranges from 4-55% (reviewed in [1]). Despite the wide ranges reported for dementia prevalence, a consistent feature of aging in DS is the progressive accumulation of AD brain pathologies. By the age of 40 years, virtually all have sufficient senile plaques and neurofibrillary tangles for a neuropathological diagnosis of AD [2]. Thus, there is dissociation between the age of onset of AD neuropathology (40 years) and increasing signs of clinical dementia. We discuss the hypothesis that frontal impairments are a critical factor affecting cognitive function and are associated with white matter (WM) and AD neuropathology. While these may be an early sign of conversion to dementia, we also review several other clinical comorbidities that may also contribute to dementia onset.

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