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Disclosure of preclinical Alzheimers disease biomarker results in research and clinical settings: Why how and what we still need to know

机译:临床前阿尔茨海默病的疾病生物标志物导致研究和临床环境:为什么如何以及我们仍然需要知道的

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摘要

Disclosure of personal disease‐related information to asymptomatic adults has been debated over the last century in medicine and research. Recently, Alzheimer's disease (AD) has been conceptualized as a continuum that begins with a “preclinical” stage in which biomarkers are present in the absence of cognitive impairment. Studies have begun assessing the safety, psychological, and behavioral effects of disclosing both AD‐related genetic and biomarker information to cognitively unimpaired older adults. Yet, debate continues over the appropriate circumstances and methods for returning such information. This article outlines concerns with and rationale for AD biomarker disclosure and summarizes findings from prior studies. Overall, this article aims to describe and respond to key questions concerning disclosure of amyloid positron emission tomography scan results to asymptomatic adults in a research setting. Moving forward, such conditions are important to consider as interventions target the preclinical phase of AD and normalize disclosing biomarker information to cognitively unimpaired persons.
机译:在上个世纪在医学和研究中,披露对无症状成人的个人疾病相关信息已经辩论。最近,阿尔茨海默病(AD)被概念化为一个连续体,以“临床前”阶段开始,在没有认知障碍的情况下存在生物标志物。研究已经开始评估披露与涉及相关遗传和生物标志物信息的安全性,心理和行为效应,以认知未受吸引人的老年人。然而,在返回此类信息的适当情况和方法中继续辩论。本文概述了AD生物标志物披露的担忧和理由,并总结了先前研究的结果。总体而言,本文旨在描述和响应关于淀粉样蛋白正电子发射断层摄影扫描结果的关键问题,在研究环境中对无症状成人进行透析。向前发展,这种条件是值得考虑的,因为干预率瞄准广告的临床前阶段,并将披露生物标志物信息的正常化以认知未受损人员。

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