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基于“我们所有人”数据对林奇综合征人群筛查的影响洞察

Impact of population screening for Lynch syndrome insights from the All of Us data.

作者信息

Park Jiheum, Karnati Hemanth, Rustgi Sheila D, Hur Chin, Kong Xiao-Fei, Kastrinos Fay

机构信息

Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

Nat Commun. 2025 Jan 9;16(1):523. doi: 10.1038/s41467-024-52562-5.

Abstract

Lynch Syndrome (LS) is a common genetic cancer condition that allows for personalized cancer prevention and early cancer detection in identified gene carriers. We used data from the All of Us (AOU) Research Initiative to assess the prevalence of LS in the general U.S. population, and analyzed demographic, personal, and family cancer history, stratified by LS genotype to compare LS and non-LS carriers. The results suggest that population-based germline testing for LS may identify up to 63.2% of carriers who might remain undetected due to lack of personal or family cancer history. LS affects about 1 in 354 individuals in this U.S. cohort, where pathogenic variants in the genes MSH6 and PMS2 account for the majority of cases. These results underscore the need to optimize the identification of LS across diverse populations and population-based germline testing may capture the most individuals who can benefit from precision cancer screening and prevention.

摘要

林奇综合征(LS)是一种常见的遗传性癌症疾病,能够对已确定的基因携带者进行个性化癌症预防和早期癌症检测。我们使用了“我们所有人(AOU)”研究计划的数据来评估美国普通人群中LS的患病率,并分析了人口统计学、个人及家族癌症病史,按LS基因型分层以比较LS携带者和非LS携带者。结果表明,基于人群的LS种系检测可能会识别出高达63.2%因缺乏个人或家族癌症病史而可能未被发现的携带者。在这个美国队列中,LS影响约每354人中的1人,其中基因MSH6和PMS2中的致病变异占大多数病例。这些结果强调了在不同人群中优化LS识别的必要性,基于人群的种系检测可能会涵盖最多能从精准癌症筛查和预防中受益的个体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/036f/11718231/db4115387bf0/41467_2024_52562_Fig1_HTML.jpg

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