Alzheimer's Therapeutic Research Institute (ATRI), Keck School of Medicine, University of Southern California, 9860 Mesa Rim Road, San Diego, CA, 92121, USA.
CNS Drugs. 2020 Aug;34(8):785-794. doi: 10.1007/s40263-020-00740-6.
Individuals with Down syndrome (DS) are at high risk for developing Alzheimer's disease (AD) pathology and this has provided significant insights into our understanding of the genetic basis of AD. The present review summarizes recent clinical, neuropathologic, imaging, and fluid biomarker studies of AD in DS (DSAD), highlighting the striking similarities, as well as some notable differences, between DSAD and the more common late-onset form of AD (LOAD) in the general population, as well as the much rarer, autosomal-dominant form of AD (ADAD). There has been significant progress in our understanding of the natural history of AD biomarkers in DS and their relationship to clinically meaningful changes. Additional work is needed to clearly define the continuum of AD that has been described in the general population, such as the preclinical, prodromal, and dementia stages of AD. Multiple therapeutic approaches, including those targeting not only β-amyloid but also tau and the amyloid precursor protein itself, require consideration. Recent developments in the field are presented within the context of such efforts to conduct clinical trials to treat and potentially prevent AD in DS.
唐氏综合征(DS)患者发生阿尔茨海默病(AD)病理的风险很高,这为我们了解 AD 的遗传基础提供了重要线索。本综述总结了 DS 中 AD(DSAD)的近期临床、神经病理学、影像学和液生物标志物研究,突出了 DSAD 与更常见的一般人群中晚发性 AD(LOAD)之间的显著相似性,以及更罕见的常染色体显性 AD(ADAD)之间的一些显著差异。我们对 DS 中 AD 生物标志物的自然史及其与具有临床意义的变化的关系有了更深入的了解。需要开展更多的工作来明确定义已在一般人群中描述的 AD 连续体,例如 AD 的临床前、前驱和痴呆阶段。需要考虑多种治疗方法,包括不仅针对β-淀粉样蛋白,还针对 tau 和淀粉样前体蛋白本身的方法。本文在开展临床试验以治疗和潜在预防 DS 中 AD 的努力背景下介绍了该领域的最新进展。