Laboratory of Neuroimaging of Aging (LANVIE), University Hospitals and University of Geneva, Geneva, Switzerland; Department of Internal Medicine, University Hospitals and University of Geneva, Geneva, Switzerland.
Laboratory of Neuroimaging of Aging (LANVIE), University Hospitals and University of Geneva, Geneva, Switzerland; Laboratory of Alzheimer Neuroimaging and Epidemiology (LANE), IRCCS S Giovanni di Dio-Fatebenefratelli, Brescia, Italy.
Lancet Neurol. 2017 Aug;16(8):661-676. doi: 10.1016/S1474-4422(17)30159-X. Epub 2017 Jul 11.
The diagnosis of Alzheimer's disease can be improved by the use of biological measures. Biomarkers of functional impairment, neuronal loss, and protein deposition that can be assessed by neuroimaging (ie, MRI and PET) or CSF analysis are increasingly being used to diagnose Alzheimer's disease in research studies and specialist clinical settings. However, the validation of the clinical usefulness of these biomarkers is incomplete, and that is hampering reimbursement for these tests by health insurance providers, their widespread clinical implementation, and improvements in quality of health care. We have developed a strategic five-phase roadmap to foster the clinical validation of biomarkers in Alzheimer's disease, adapted from the approach for cancer biomarkers. Sufficient evidence of analytical validity (phase 1 of a structured framework adapted from oncology) is available for all biomarkers, but their clinical validity (phases 2 and 3) and clinical utility (phases 4 and 5) are incomplete. To complete these phases, research priorities include the standardisation of the readout of these assays and thresholds for normality, the evaluation of their performance in detecting early disease, the development of diagnostic algorithms comprising combinations of biomarkers, and the development of clinical guidelines for the use of biomarkers in qualified memory clinics.
生物标志物可以改善阿尔茨海默病的诊断。通过神经影像学(如 MRI 和 PET)或脑脊液分析评估的功能障碍、神经元丧失和蛋白沉积的生物标志物,越来越多地用于在研究和专科临床环境中诊断阿尔茨海默病。然而,这些生物标志物的临床实用性的验证并不完整,这阻碍了医疗保险提供者对这些检测的报销、它们的广泛临床实施以及医疗保健质量的提高。我们从癌症生物标志物的方法中开发了一个促进阿尔茨海默病生物标志物临床验证的战略五阶段路线图。所有生物标志物都具有足够的分析有效性证据(改编自肿瘤学的结构化框架的第 1 阶段),但它们的临床有效性(第 2 和第 3 阶段)和临床实用性(第 4 和第 5 阶段)并不完整。为了完成这些阶段,研究重点包括这些检测的读数和正常范围的标准化,评估它们在检测早期疾病中的性能,开发包含生物标志物组合的诊断算法,以及制定合格记忆诊所中使用生物标志物的临床指南。