The importance of the dyad: Participant perspectives on sharing biomarker results in Alzheimer's disease research

被引:4
作者
Ketchum, Fred B. [1 ]
Chin, Nathaniel A. [2 ,3 ]
Erickson, Claire [4 ]
Lambrou, Nickolas H. [2 ]
Basche, Kristin [2 ]
Gleason, Carey E. [2 ,3 ,5 ]
Clark, Lindsay [2 ,3 ,5 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Neurol, 1675 Highland, Madison, WI 53705 USA
[2] Univ Wisconsin, Dept Med, Div Geriatr, Sch Med & Publ Hlth, Madison, WI 53705 USA
[3] Wisconsin Alzheimers Dis Res Ctr, Madison, WI USA
[4] Univ Penn, Dept Med Ethics & Hlth Policy, Perelman Sch Med, Philadelphia, PA USA
[5] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI USA
关键词
Alzheimer's disease; biomarkers; disclosure; ethics; preclinical diagnosis; DEMENTIA; STIGMA;
D O I
10.1002/trc2.12416
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUNDIn the asymptomatic "preclinical" phase of Alzheimer's disease (AD), abnormal biomarkers indicate risk for developing cognitive impairment. Biomarker information is increasingly being disclosed to participants in research settings, and biomarker testing and results disclosure will be implemented in clinical settings in the future. Biomarker disclosure has potential psychosocial benefits and harms, impacting affected individuals and their support person(s). Limited data are available about with whom research participants share their results, information that will be necessary to develop disclosure protocols and post-disclosure resources. Additionally, existing research has been conducted in largely White cohorts, limiting applicability to future clinical populations. METHODSWe enrolled a diverse cohort of 329 adults (184 non-Hispanic White and 145 Black/African American individuals) who previously participated in AD research. After reviewing a vignette describing a hypothetical biomarker research study, participants indicated their anticipated willingness to share biomarker results with loved ones, and what reactions they anticipated from others. Using mixed-methods analysis, we identified responses related to willingness to share results. RESULTSA majority (78.7%) were willing to share their results with support persons. Many (59.6%) felt it would not be difficult to share, and most (90.6%) believed their loved ones would be supportive. The most common reasons for sharing were to prepare for possible future AD (41.0% of respondents), while the most common reason for not sharing was to avoid worrying loved ones (4.8% of respondents). A total of 7.3% of respondents related reasons regarding being unsure about sharing. DISCUSSIONParticipants' interest in sharing results supports integrating support persons into AD biomarker research, and may help maximize potential benefits for participants. Communicating with this "dyad" of research participant and support person(s) may improve involvement in research, and help prepare for implementation of clinical biomarker testing by clarifying communication preferences and the influence of support persons on psychosocial outcomes.
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页数:11
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