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

被引:48
作者
Erickson, Claire M. [1 ,2 ]
Chin, Nathaniel A. [2 ]
Johnson, Sterling C. [2 ,3 ,4 ]
Gleason, Carey E. [2 ,4 ]
Clark, Lindsay R. [2 ,3 ,4 ]
机构
[1] Univ Wisconsin, Neurosci & Publ Policy Program, Sch Med & Publ Hlth, Madison, WI USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Alzheimers Dis Res Ctr, Madison, WI USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Alzheimers Inst, Madison, WI USA
[4] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI USA
关键词
Alzheimer' s disease; amyloid positron emission tomography; disclosure; future directions; personal impact; research impact; POSITRON-EMISSION-TOMOGRAPHY; COGNITIVE IMPAIRMENT; APOE GENOTYPE; RISK; SAFETY;
D O I
10.1002/dad2.12150
中图分类号
R74 [神经病学与精神病学];
学科分类号
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.
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页数:15
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