Hadar Adva, Gurwitz David
Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine.
Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv 69978 Israel.
Dialogues Clin Neurosci. 2018 Dec;20(4):293-300. doi: 10.31887/DCNS.2018.20.4/dgurwitz.
Alzheimer disease (AD) is the major epidemic of the 21 century, its prevalence rising along with improved human longevity. Early AD diagnosis is key to successful treatment, as currently available therapeutics only allow small benefits for diagnosed AD patients. By contrast, future therapeutics, including those already in preclinical or clinical trials, are expected to afford neuroprotection prior to widespread brain damage and dementia. Brain imaging technologies are developing as promising tools for early AD diagnostics, yet their high cost limits their utility for screening at-risk populations. Blood or plasma transcriptomics, proteomics, and/or metabolomics may pave the way for cost-effective AD risk screening in middle-aged individuals years ahead of cognitive decline. This notion is exemplified by data mining of blood transcriptomics from a published dataset. Consortia blood sample collection and analysis from large cohorts with mild cognitive impairment followed longitudinally for their cognitive state would allow the development of a reliable and inexpensive early AD screening tool.
阿尔茨海默病(AD)是21世纪的主要流行病,其患病率随着人类寿命的延长而上升。早期AD诊断是成功治疗的关键,因为目前可用的治疗方法仅能给已确诊的AD患者带来微小益处。相比之下,未来的治疗方法,包括那些已经处于临床前或临床试验阶段的方法,有望在广泛的脑损伤和痴呆症发生之前提供神经保护作用。脑成像技术正在发展成为早期AD诊断的有前景的工具,但其高昂的成本限制了它们在高危人群筛查中的应用。血液或血浆转录组学、蛋白质组学和/或代谢组学可能为在中年个体出现认知衰退前数年进行具有成本效益的AD风险筛查铺平道路。已发表数据集中血液转录组学的数据挖掘就例证了这一观点。对有轻度认知障碍的大型队列进行纵向跟踪其认知状态的联合血液样本采集和分析,将有助于开发出一种可靠且廉价的早期AD筛查工具。