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将种族因素纳入阿尔茨海默病的遗传风险评估:REVEAL研究经验

Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.

作者信息

Christensen Kurt D, Roberts J Scott, Royal Charmaine D M, Fasaye Grace-Ann, Obisesan Thomas, Cupples L Adrienne, Whitehouse Peter J, Butson Melissa Barber, Linnenbringer Erin, Relkin Norman R, Farrer Lindsay, Cook-Deegan Robert, Green Robert C

机构信息

Department of Health Behavior and Health Education, University of Michigan School of Public Health, Ann Arbor, Michigan 48109-0471, USA.

出版信息

Genet Med. 2008 Mar;10(3):207-14. doi: 10.1097/GIM.0b013e318164e4cf.

Abstract

PURPOSE

To describe how investigators in a multisite randomized clinical trial addressed scientific and ethical issues involved in creating risk models based on genetic testing for African American participants.

METHODS

The following informed our decision whether to stratify risk assessment by ethnicity: evaluation of epidemiological data, appraisal of benefits and risks of incorporating ethnicity into calculations, and feasibility of creating ethnicity-specific risk curves. Once the decision was made, risk curves were created based on data from a large, diverse study of first-degree relatives of patients with Alzheimer disease.

RESULTS

Review of epidemiological data suggested notable differences in risk between African Americans and whites and that Apolipoprotein E genotype predicts risk in both groups. Discussions about the benefits and risks of stratified risk assessments reached consensus that estimates based on data from whites should not preclude enrolling African Americans, but population-specific risk curves should be created if feasible. Risk models specific to ethnicity, gender, and Apolipoprotein E genotype were subsequently developed for the randomized clinical trial that oversampled African Americans.

CONCLUSION

The Risk Evaluation and Education for Alzheimer Disease study provides an instructive example of a process to develop risk assessment protocols that are sensitive to the implications of genetic testing for multiple ethnic groups with differing levels of risk.

摘要

目的

描述多中心随机临床试验中的研究人员如何解决在为非裔美国参与者进行基于基因检测的风险模型构建过程中所涉及的科学和伦理问题。

方法

以下因素影响了我们关于是否按种族对风险评估进行分层的决定:流行病学数据评估、将种族纳入计算的利弊评估以及创建特定种族风险曲线的可行性。一旦做出决定,便基于对阿尔茨海默病患者一级亲属的一项大型多样化研究的数据创建风险曲线。

结果

流行病学数据回顾表明非裔美国人和白人之间在风险上存在显著差异,且载脂蛋白E基因型在两组中均能预测风险。关于分层风险评估利弊的讨论达成共识,即基于白人数据的估计不应排除非裔美国人入组,但如果可行,应创建特定人群的风险曲线。随后为该对非裔美国人进行了过度抽样的随机临床试验开发了针对种族、性别和载脂蛋白E基因型的风险模型。

结论

阿尔茨海默病风险评估与教育研究为制定对具有不同风险水平的多个种族群体的基因检测影响敏感的风险评估方案的过程提供了一个具有启发性的范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d912/2483343/8907e9c809d5/nihms-57716-f0001.jpg

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