Frontiers in Operations: Optimal Genetic Testing of Families

Daniel Adelman, Kanix Wang
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Abstract

Problem definition: Through the laws of inheritance, knowing an individual’s genetic status informs disease risk for family members, but current protocols for deciding whom to genetically test only consider one person at a time rather than design an optimal testing plan for the entire family. Methodology/results: We develop a Markov decision process framework for maximizing the net benefits of genetic testing that integrates a Bayesian network of genetic statuses, with a functional representation of cost-effectiveness. Our model provides a contingent sequence of family members to test one at a time, that is, a plan that dynamically incorporates new test results, revealed sequentially at random, to decide who next to test. In the general case, we show that optimal stopping follows a structure with two-sided thresholds, previously known only for individual testing. Although the optimal testing sequence, in general, is contingent on the family test results, in the special case of sibling-only tests we can identify this sequence a priori. Our numerical case study, which was conducted in a realistic BRCA1/2 testing setting, demonstrates that an optimal policy significantly improves cost-effectiveness over existing policies. Thus, our framework offers a promising and powerful new approach to genetic testing. Managerial implications: In an optimal policy, prioritizing testing family members who might otherwise not have been tested can lead to an overall improvement in familial health value, surpassing even the most cost-effective existing protocols. From a management perspective, healthcare organizations and insurance companies can potentially save costs by implementing this approach for such families. History: This paper has been accepted in the Manufacturing & Service Operations Management Frontiers in Operations Initiative. Funding: D. Adelman is grateful for financial support from Booth School of Business. Supplemental Material: The online appendix is available at https://doi.org/10.1287/msom.2023.0057 .
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业务前沿:最佳家庭基因检测
问题的定义:通过遗传规律,了解个人的基因状况可告知家庭成员的疾病风险,但目前决定对谁进行基因检测的方案每次只考虑一个人,而不是为整个家庭设计最佳检测计划。方法/结果:我们开发了一个马尔可夫决策过程框架,用于实现基因检测净效益的最大化,该框架将基因状态的贝叶斯网络与成本效益的功能表示相结合。我们的模型提供了一个每次检测一个家庭成员的或然序列,即一个动态纳入随机顺序揭示的新检测结果的计划,以决定下一个检测对象。在一般情况下,我们证明了最优停止遵循一个具有双面阈值的结构,而这种结构以前只为个人测试所知。虽然一般情况下,最佳测试顺序取决于家族测试结果,但在只有兄弟姐妹测试的特殊情况下,我们可以先验地确定这一顺序。我们在现实的 BRCA1/2 检测环境中进行了数值案例研究,结果表明,与现有政策相比,最优政策能显著提高成本效益。因此,我们的框架为基因检测提供了一种前景广阔、功能强大的新方法。管理意义:在最优政策中,优先对那些可能不会接受检测的家庭成员进行检测,可全面提高家族健康价值,甚至超过最具成本效益的现有方案。从管理的角度来看,医疗机构和保险公司通过对这些家庭实施这种方法,有可能节约成本。历史:本文已被《制造与服务运营管理》(Manufacturing & Service Operations Management)的 "运营前沿"(Frontiers in Operations Initiative)杂志录用。资助:D. Adelman 感谢布斯商学院的资助。补充材料:在线附录见 https://doi.org/10.1287/msom.2023.0057 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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