妇女向直系亲属和旁系亲属告知最新基因检测结果的意向预测因素。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2023-01-01 Epub Date: 2023-01-14 DOI:10.1159/000528522
Carolyn Winskill, Melody S Goodman, Brianne M Daly, Ashley Elrick, Ryan Mooney, Whitney Espinel, Wendy Kohlmann, Kimberly A Kaphingst
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引用次数: 0

摘要

介绍:许多之前基因检测结果呈阴性的人都有资格接受最新检测。本研究考察了之前基因检测结果为阴性的参与者向亲属告知最新基因检测结果的意向:方法:在 2018 年 4 月至 2019 年 10 月期间,招募了有个人或家族乳腺癌或卵巢癌病史且在 2013 年之前 BRCA1/2 检测结果为阴性的女性。计算比例以评估向在世直系亲属、大家庭和所有家庭传达最新基因检测结果的意向。评估了计划行为理论中潜在的意向预测因素(态度、主观规范、感知行为控制)。使用准二叉概率分布的广义线性模型对三种结果进行了分析:110 名妇女在更新测试前完成了基线评估。参与者打算将基因检测结果告知 90% 的直系亲属、51% 的大家庭和 66% 的所有在世亲属。主观标准较高的参与者(aOR = 1.93,95% CI:1.08-3.57)向大家庭传达基因检测结果的意愿较高,而态度较积极的参与者(aOR = 1.27,95% CI:1.01-1.60)向所有家人传达结果的意愿较高。对遗传信息的重视程度越高,向直系亲属通报的意愿就越高(aOR = 1.40,95% CI:1.06-1.83)。主观计算能力较低与向大家庭传达信息的意愿较高相关(aOR = 0.50,95% CI:0.32-0.76):结论:态度和主观规范是向高风险亲缘关系人传达最新遗传信息意愿的预测因素,而且预测因素可能因关系程度而异。
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Predictors of Women's Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members.

Introduction: Many individuals who previously received negative genetic test results are eligible for updated testing. This study examined intention to communicate updated genetic test results to relatives in participants who previously received negative genetic test results.

Methods: Women with a personal or family history of breast or ovarian cancer who tested negative for BRCA1/2 before 2013 were enrolled between April 2018 and October 2019. Proportions were calculated to assess intention to communicate updated genetic test results to living immediate family, extended family, and all family. Potential predictors of intentions from the theory of planned behavior (attitudes, subjective norms, perceived behavioral control) were assessed. The three outcomes were analyzed using generalized linear models with a quasi-binomial probability distribution.

Results: 110 women completed the baseline assessment prior to updated testing. Participants intended to communicate genetic test results to 90% of immediate family, 51% of extended family, and 66% of all living relatives. Participants with higher subjective norms (aOR = 1.93, 95% CI: 1.08-3.57) had higher intentions to communicate genetic test results to extended family, while participants with more positive attitudes (aOR = 1.27, 95% CI: 1.01-1.60) had higher intentions to communicate to all family. Placing higher importance on genetic information was associated with higher intentions to communicate to immediate family (aOR = 1.40, 95% CI: 1.06-1.83). Lower subjective numeracy was associated with higher intentions to communicate to extended family (aOR = 0.50, 95% CI: 0.32-0.76).

Conclusion: Attitudes and subjective norms were predictors of intention to communicate updated genetic information to at-risk biological relatives, and predictors may vary by degree of relationship.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
期刊最新文献
Investigating the impact of screen-sharing visual aids during genomic results disclosure via telehealth in diverse families in the TeleKidSeq pilot study. Adopting public health genomics when the house is on fire: How will we navigate to 2030? Modern Family: An Ethical Justification for System-Led Contact of Relatives Eligible for Cascade Screening in the United States. Variation Exists in Service Delivery: Similarities and Differences in the Provision of a Whole Genome Sequencing Service for Paediatric Rare Disease Patients in the National Health Service in England. Evaluating the Implementation of the Rapid Prenatal Exome Sequencing Service in England.
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