Sabbagh Marwan N, Richardson Sharon, Relkin Norman
Cleo Roberts Center for Clinical Research, Sun Health Research Institute, Sun City, AZ, USA. Marwan.
Alzheimers Dement. 2008 Jan;4(1 Suppl 1):S109-18. doi: 10.1016/j.jalz.2007.11.013.
The era of disease modification as a therapeutic option for Alzheimer's disease (AD) is upon us. With dozens of novel drugs in development, there is more need than ever to develop biomarkers that distinguish normal aging from AD and AD from other dementias, track changes over time as disease progresses, and respond to interventions. Future trials will need to weight biomarker outcomes equal to cognitive outcomes especially when the biomarkers are linked to specific mechanisms, such as changes to beta amyloid (Abeta) deposition or brain volume. Since the advent of donepezil as a treatment for AD, new mechanisms of action of this molecule have been discovered. In this perspective, we review trial design and discuss the use of biomarkers by using lessons learned from previous trials conducted with cholinergic therapy.
疾病修饰作为阿尔茨海默病(AD)治疗选择的时代已经到来。随着数十种新型药物正在研发,比以往任何时候都更需要开发生物标志物,以区分正常衰老与AD,以及AD与其他痴呆症,跟踪疾病进展过程中的变化,并对干预措施做出反应。未来的试验需要将生物标志物结果与认知结果同等重视,尤其是当生物标志物与特定机制相关联时,例如β淀粉样蛋白(Aβ)沉积或脑容量的变化。自从多奈哌齐作为AD治疗药物问世以来,已发现该分子的新作用机制。从这个角度出发,我们回顾试验设计,并通过借鉴以往胆碱能治疗试验的经验教训来讨论生物标志物的使用。