Alzheimer's Disease Cooperative Study, Department of Neurosciences, UCSD School of Medicine, La Jolla, CA 92037-0624, USA.
J Neural Transm (Vienna). 2012 Jul;119(7):843-50. doi: 10.1007/s00702-012-0772-4. Epub 2012 Feb 22.
Alzheimer's disease (AD) affects more than twenty-five million people worldwide and is the most common form of dementia. Symptomatic treatments have been developed, but effective intervention to alter disease progression is needed. Targets have been identified for disease-modifying drugs, but the results of clinical trials have been disappointing. Peripheral biomarkers of disease state may improve clinical trial design and analysis, increasing the likelihood of successful drug development. Amyloid-related measures, presumably reflecting principal pathology of AD, are among the leading cerebrospinal fluid and neuroimaging biomarkers, and measurement of plasma levels of amyloid peptides has been the focus of much investigation. In this review, we discuss recent data on plasma β-amyloid (Aβ) and examine the issues that have arisen in establishing it as a reliable biomarker of AD.
阿尔茨海默病(AD)影响着全球超过 2500 万人,是最常见的痴呆症形式。已经开发出了对症治疗方法,但需要有效的干预措施来改变疾病进展。已经确定了用于疾病修饰药物的靶点,但临床试验的结果令人失望。疾病状态的外周生物标志物可能会改善临床试验的设计和分析,从而增加药物开发成功的可能性。淀粉样蛋白相关指标,推测反映了 AD 的主要病理学,是脑脊液和神经影像学生物标志物的主要指标之一,测量淀粉样肽的血浆水平一直是许多研究的重点。在这篇综述中,我们讨论了最近关于血浆β-淀粉样蛋白(Aβ)的研究数据,并研究了将其确立为 AD 可靠生物标志物所面临的问题。