Abi Nader Clément, Ayache Nicholas, Frisoni Giovanni B, Robert Philippe, Lorenzi Marco
Université Côte d'Azur, INRIA Sophia Antipolis, EPIONE Research Project, 06902, Sophia-Antipolis, France.
Memory Clinic and LANVIE-Laboratory of Neuroimaging of Aging, Hospitals and University of Geneva, 1205, Geneva, Switzerland.
Brain Commun. 2021 Apr 28;3(2):fcab091. doi: 10.1093/braincomms/fcab091. eCollection 2021.
In this study, we investigate SimulAD, a novel quantitative instrument for the development of intervention strategies for disease-modifying drugs in Alzheimer's disease. SimulAD is based on the modeling of the spatio-temporal dynamics governing the joint evolution of imaging and clinical biomarkers along the history of the disease, and allows the simulation of the effect of intervention time and drug dosage on the biomarkers' progression. When applied to multi-modal imaging and clinical data from the Alzheimer's Disease Neuroimaging Initiative the method enables to generate hypothetical scenarios of amyloid lowering interventions. The results quantify the crucial role of intervention time, and provide a theoretical justification for testing amyloid modifying drugs in the pre-clinical stage. Our experimental simulations are compatible with the outcomes observed in past clinical trials, and suggest that anti-amyloid treatments should be administered at least 7 years earlier than what is currently being done in order to obtain statistically powered improvement of clinical endpoints.
在本研究中,我们对SimulAD进行了研究,它是一种用于开发阿尔茨海默病疾病修饰药物干预策略的新型定量工具。SimulAD基于对疾病发展过程中影像和临床生物标志物联合演变的时空动力学建模,并能模拟干预时间和药物剂量对生物标志物进展的影响。当应用于来自阿尔茨海默病神经影像倡议组织的多模态影像和临床数据时,该方法能够生成淀粉样蛋白降低干预的假设情景。结果量化了干预时间的关键作用,并为在临床前阶段测试淀粉样蛋白修饰药物提供了理论依据。我们的实验模拟与过去临床试验中观察到的结果相符,并表明抗淀粉样蛋白治疗应比目前的治疗时间至少提前7年进行,以便在临床终点上获得具有统计学效力的改善。