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基于生物标志物的阿尔茨海默病诊断。1. 伦理和社会问题。

The biomarker-based diagnosis of Alzheimer's disease. 1-ethical and societal issues.

作者信息

Porteri Corinna, Albanese Emiliano, Scerri Charles, Carrillo Maria C, Snyder Heather M, Martensson Birgitta, Baker Mark, Giacobini Ezio, Boccardi Marina, Winblad Bengt, Frisoni Giovanni B, Hurst Samia

机构信息

Bioethics Unit, IRCCS Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy.

Department of Psychiatry, WHO Collaborating Centre, University of Geneva, Switzerland.

出版信息

Neurobiol Aging. 2017 Apr;52:132-140. doi: 10.1016/j.neurobiolaging.2016.07.011.

Abstract

There is great interest in the use of biomarkers to assist in the timely identification of Alzheimer's disease (AD) in individuals with mild symptoms. However, the inclusion of AD biomarkers in clinical criteria poses socioethical challenges. The Geneva Task Force for the Roadmap of Alzheimer's Biomarkers was established to deliver a systematic strategic research agenda (aka roadmap) to promote efficient and effective validation of AD biomarkers and to foster their uptake in clinical practice. In this article, we summarize the workshop discussion of the Geneva Task Force "ethical and societal issues" working group, which comprised bioethicists, clinicians, health economists, and representatives of those affected by AD. The working group identified the following key issues that need to be included in the roadmap: improving access to services through timely diagnosis, the need for a diagnostic research protocol before moving to clinical routine, recruitment in diagnostic research protocols in the absence of effective therapy, respect for the autonomy of the individual with mild cognitive impairment in information and consent process and the right not to know biomarkers results, need for counseling programs, disclosure of the diagnosis in a structured environment and the involvement of family members, health policies including the individuals' views and the protection of their interests, and the economic costs for society.

摘要

人们对使用生物标志物协助及时识别有轻微症状个体的阿尔茨海默病(AD)有着浓厚兴趣。然而,在临床标准中纳入AD生物标志物带来了社会伦理挑战。阿尔茨海默病生物标志物路线图日内瓦特别工作组的成立是为了提供一个系统的战略研究议程(即路线图),以促进对AD生物标志物进行高效且有效的验证,并推动其在临床实践中的应用。在本文中,我们总结了日内瓦特别工作组“伦理和社会问题”工作组的研讨会讨论内容,该工作组由生物伦理学家、临床医生、卫生经济学家以及AD患者代表组成。该工作组确定了以下需要纳入路线图的关键问题:通过及时诊断改善服务可及性;在进入临床常规之前需要一个诊断研究方案;在缺乏有效治疗方法的情况下进行诊断研究方案的招募;在信息和同意过程中尊重轻度认知障碍个体的自主权以及不知道生物标志物结果的权利;需要咨询项目;在结构化环境中披露诊断结果以及家庭成员的参与;包括个体观点和保护其利益的卫生政策;以及对社会的经济成本。

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