A conceptual framework and ethics analysis for prevention trials of Alzheimer Disease

被引:18
|
作者
Peters, Kevin R. [1 ]
Beattie, B. Lynn [2 ]
Feldman, Howard H. [3 ]
Illes, Judy [4 ]
机构
[1] Trent Univ, Dept Psychol, Peterborough, ON K9J 7B8, Canada
[2] Univ British Columbia, Dept Med, Div Geriatr Med, Vancouver, BC, Canada
[3] Univ British Columbia, Dept Med, Div Neurol, Vancouver, BC V6T 1W5, Canada
[4] Univ British Columbia, Natl Core Neuroeth, Vancouver, BC V5Z 1M9, Canada
关键词
Alzheimer Disease; Prevention; Treatment; Biomarkers; Ethics; MILD COGNITIVE IMPAIRMENT; BRAIN IMAGING RESEARCH; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; INCIDENTAL FINDINGS; RANDOMIZED-TRIAL; RISK-FACTORS; DEMENTIA; RECOMMENDATIONS;
D O I
10.1016/j.pneurobio.2012.12.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
As our understanding of the neurobiology of Alzheimer Disease deepens, it has become evident that early intervention is critical to achieving successful therapeutic impact. The availability of diagnostic criteria for preclinical Alzheimer Disease adds momentum to research directed at this goal and even to prevention. The landscape of therapeutic research is thus poised to undergo a dramatic shift in the next 5-10 years, with clinical trials involving subjects at risk for Alzheimer Disease who have few or no symptoms. These trials will also likely rely heavily on genetics, biomarkers, and or risk factor stratification to identify individuals at risk for Alzheimer Disease. Here, we propose a conceptual framework to guide this next generation of pharmacological and non-pharmacological clinical pursuit, and discuss some of the foreseeable ethical considerations that may accompany them. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:114 / 123
页数:10
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