Langlois Carolyn M, Bradbury Angela, Wood Elisabeth M, Roberts J Scott, Kim Scott Y H, Riviere Marie-Emmanuelle, Liu Fonda, Reiman Eric M, Tariot Pierre N, Karlawish Jason, Langbaum Jessica B
Banner Alzheimer's Institute, Phoenix, AZ, USA.
Department of Medical Ethics and Health Policy, University of Pennsylvania, Philadelphia, PA, USA.
Alzheimers Dement (N Y). 2019 Nov 6;5:705-716. doi: 10.1016/j.trci.2019.09.013. eCollection 2019.
As the number of Alzheimer's disease (AD) prevention studies grows, many individuals will need to learn their genetic and/or biomarker risk for the disease to determine trial eligibility. An alternative to traditional models of genetic counseling and disclosure is needed to provide comprehensive standardized counseling and disclosure of apolipoprotein E () results efficiently, safely, and effectively in the context of AD prevention trials.
A multidisciplinary Genetic Testing, Counseling, and Disclosure Committee was established and charged with operationalizing the Alzheimer's Prevention Initiative (API) Genetic Counseling and Disclosure Process for use in the API Generation Program trials. The objective was to provide consistent information to research participants before and during the counseling and disclosure session using standardized educational and session materials.
The Genetic Testing, Counseling, and Disclosure Committee created a process consisting of eight components: requirements of testing and reports, psychological readiness assessment, determination of AD risk estimates, guidance for identifying providers of disclosure, predisclosure education, counseling and disclosure session materials, counseling and disclosure session flow, and assessing disclosure impact.
The API Genetic Counseling and Disclosure Process provides a framework for large-scale disclosure of genotype results to study participants and serves as a model for disclosure of biomarker results. The process provides education to participants about the meaning and implication(s) of their results while also incorporating a comprehensive assessment of disclosure impact. Data assessing participant safety and psychological well-being before and after disclosure are still being collected and will be presented in a future publication.
随着阿尔茨海默病(AD)预防研究数量的增加,许多人需要了解自己患该疾病的遗传和/或生物标志物风险,以确定是否符合试验条件。需要一种替代传统遗传咨询和结果告知模式的方法,以便在AD预防试验的背景下,高效、安全且有效地提供关于载脂蛋白E()结果的全面标准化咨询和结果告知。
成立了一个多学科的基因检测、咨询和结果告知委员会,负责实施阿尔茨海默病预防计划(API)基因咨询和结果告知流程,以用于API代际项目试验。目标是在咨询和结果告知环节之前及期间,使用标准化的教育材料和环节材料,向研究参与者提供一致的信息。
基因检测、咨询和结果告知委员会创建了一个由八个部分组成的流程:检测和报告的要求、心理准备评估、AD风险估计的确定、确定结果告知提供者的指导、结果告知前教育、咨询和结果告知环节材料、咨询和结果告知环节流程以及评估结果告知的影响。
API基因咨询和结果告知流程为向研究参与者大规模披露基因型结果提供了一个框架,并可作为生物标志物结果披露的模式。该流程向参与者提供关于其结果的意义和影响的教育,同时还纳入了对结果告知影响的全面评估。目前仍在收集评估结果告知前后参与者安全性和心理健康状况的数据,这些数据将在未来的出版物中呈现。