Racine Eric, Forlini Cynthia, Aspler John, Chandler Jennifer
Institut de recherches cliniques de Montréal, Neuroethics Research Unit, Montréal, QC, Canada.
Université de Montréal, Department of Medicine and Department of Social and Preventive Medicine, Montréal, QC, Canada.
J Alzheimers Dis. 2016;51(1):1-9. doi: 10.3233/JAD-150534.
Preclinical Alzheimer's disease (AD), a newly proposed, actively researched, and hotly debated research-only diagnostic category, raises the prospect of an ethical dilemma: whether, and possibly how, to treat a disorder with no target symptoms. This proposed category rests on the detection of a number of biomarkers thought to provide evidence of AD pathophysiology years before any behavioral symptoms manifest. Faced with limited treatment options, patients and their relatives may come to consider complementary and alternative medicine (CAM) a viable option, albeit one with minimal supporting evidence. Accordingly, the hopes and needs of some preclinical patients and their relatives could further fuel market-oriented entrepreneurship for CAM. In this ethics review, we provide background and reflect on some ethical questions related to the roles of key stakeholders arising from the potential for CAM use in the context of a possible preclinical AD diagnosis.
临床前阿尔茨海默病(AD)是一个新提出的、正在积极研究且备受争议的仅用于研究的诊断类别,它引发了一个伦理困境:是否以及可能如何治疗一种没有目标症状的疾病。这个提议的类别基于在任何行为症状出现之前数年检测到的一些生物标志物,这些生物标志物被认为可提供AD病理生理学的证据。面对有限的治疗选择,患者及其亲属可能会认为补充和替代医学(CAM)是一个可行的选择,尽管支持证据很少。因此,一些临床前患者及其亲属的希望和需求可能会进一步推动CAM的市场化创业。在这篇伦理评论中,我们提供背景信息,并思考一些与关键利益相关者的角色相关的伦理问题,这些问题源于在可能的临床前AD诊断背景下使用CAM的可能性。