Psychosocial Research Group, Prince of Wales Clinical School, UNSW Australia, Sydney, Australia.
The Kinghorn Cancer Centre and Cancer Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
J Genet Couns. 2021 Jun;30(3):849-860. doi: 10.1002/jgc4.1384. Epub 2021 Jan 19.
Polygenic risk scores (PRS) are personalized assessments of disease risk based on the cumulative effect of common low-risk genetic variants. PRS have been shown to accurately predict women's breast cancer risk and are likely to be incorporated into personalized breast cancer risk management programs. However, there are few studies investigating the individual impact of receiving a breast cancer PRS. Existing studies have not demonstrated significant changes in perceived risk or risk management behaviors after receipt of polygenic risk information. The aim of this qualitative study was to explore how women with a family history of breast cancer construct breast cancer risk perceptions after receipt of a breast cancer PRS. Unaffected women with a family history of breast cancer who had not previously received genetic counseling regarding their breast cancer risk were invited to participate in this study. In-depth, semi-structured interviews were conducted with 20 women who attended a familial cancer clinic in the Australian states of Victoria and Tasmania. Data were analyzed using an inductive thematic approach. Women's lived experience played a significant role in the construction and maintenance of their breast cancer risk perception. Women's pre-existing risk perceptions were informed by their family history and their knowledge that breast cancer is a multifactorial disease. Knowing that breast cancer is a multifactorial disease enabled most women to integrate genetic information with their pre-existing notions of risk. Women reported that the information they received was consistent with their existing notions of personal risk and screening advice. Therefore, the PRS did not lead to a change in perceived risk or risk management behaviors for most women. The results of this study provide insight into how polygenic risk information is integrated with pre-existing notions of risk, which will inform its implementation into clinical practice.
多基因风险评分(PRS)是基于常见低风险遗传变异的累积效应对疾病风险进行的个性化评估。PRS 已被证明可以准确预测女性的乳腺癌风险,并且很可能被纳入个性化乳腺癌风险管理计划中。然而,目前关于接受乳腺癌 PRS 对个体影响的研究较少。现有研究表明,在收到多基因风险信息后,女性的风险感知或风险管理行为并未发生显著变化。本研究旨在探讨有乳腺癌家族史的女性在收到乳腺癌 PRS 后如何构建乳腺癌风险感知。本研究邀请了没有接受过遗传咨询的有乳腺癌家族史的无病女性参加。在澳大利亚维多利亚州和塔斯马尼亚州的家族癌症诊所对 20 名女性进行了深入的半结构化访谈。采用归纳主题分析方法对数据进行分析。女性的生活经历在构建和维持其乳腺癌风险感知方面发挥了重要作用。女性的预先存在的风险感知受到家族史和乳腺癌是一种多因素疾病的知识的影响。大多数女性知道乳腺癌是一种多因素疾病,这使她们能够将遗传信息与她们预先存在的风险观念结合起来。女性报告说,她们收到的信息与她们现有的个人风险观念和筛查建议一致。因此,对于大多数女性来说,PRS 并没有导致风险感知或风险管理行为的改变。本研究的结果深入了解了多基因风险信息如何与预先存在的风险观念相融合,这将为其在临床实践中的应用提供信息。