Suppr超能文献

基于生物标志物的阿尔茨海默病诊断。2. 肿瘤学的经验教训。

The biomarker-based diagnosis of Alzheimer's disease. 2-lessons from oncology.

作者信息

Boccardi Marina, Gallo Valentina, Yasui Yutaka, Vineis Paolo, Padovani Alessandro, Mosimann Urs, Giannakopoulos Panteleimon, Gold Gabriel, Dubois Bruno, Jack Clifford R, Winblad Bengt, Frisoni Giovanni B, Albanese Emiliano

机构信息

Department of Psychiatry, LANVIE-Laboratory of Neuroimaging of Aging, University of Geneva, Geneva, Switzerland; Laboratory of Alzheimer's Neuroimaging and Epidemiology (LANE), IRCCS S.Giovanni di Dio-Fatebenefratelli, Brescia, Italy.

Centre of Primary Care and Public Health, Queen Mary, University of London, Barts and the London School of Medicine, Blizard Institute, London, UK.

出版信息

Neurobiol Aging. 2017 Apr;52:141-152. doi: 10.1016/j.neurobiolaging.2017.01.021.

Abstract

Biomarkers for the diagnosis of Alzheimer's disease (AD) are not yet validated for use in clinical settings. We aim to provide a methodological framework for their systematic validation, by reference to that developed for oncology biomarkers. As for this discipline, the steps for the systematic validation of AD biomarkers need to target analytical validity, clinical validity, and clinical utility. However, the premises are different from oncology: the nature of disease (neurodegeneration vs. cancer), the purpose (improve diagnosis in clinically affected vs. screening preclinical individuals), and the target population (mild cognitive impairment patients referring to memory clinics vs. general population) lead to important differences, influencing both the design of validation studies and the use of selected biomarkers. This framework is applied within a wider initiative to assess the current available evidence on the clinical validity of biomarkers for AD, for the final aim to identify gaps and research priorities, and to inform coordinated research efforts boosting AD biomarkers research.

摘要

用于阿尔茨海默病(AD)诊断的生物标志物尚未在临床环境中得到验证。我们旨在通过参考肿瘤生物标志物的验证方法,为AD生物标志物的系统验证提供一个方法框架。对于这一学科而言,AD生物标志物系统验证的步骤需要针对分析有效性、临床有效性和临床实用性。然而,其前提与肿瘤学不同:疾病的性质(神经退行性变与癌症)、目的(改善临床患者的诊断与筛查临床前个体)以及目标人群(转诊至记忆门诊的轻度认知障碍患者与普通人群)导致了重要差异,这既影响验证研究的设计,也影响所选生物标志物的使用。该框架应用于一项更广泛的计划中,以评估目前关于AD生物标志物临床有效性的现有证据,最终目的是识别差距和研究重点,并为推动AD生物标志物研究的协调研究工作提供信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验