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首页> 外文期刊>Journal of Genetic Counseling >Family Communication of BRCA1/2 Results and Family Uptake of BRCA1/2 Testing in a Diverse Population of BRCA1/2 Carriers
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Family Communication of BRCA1/2 Results and Family Uptake of BRCA1/2 Testing in a Diverse Population of BRCA1/2 Carriers

机译:不同人群携带的BRCA1 / 2携带者的BRCA1 / 2结果的家庭交流和BRCA1 / 2检测的家庭摄取。

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摘要

Previous studies examining communication of BRCA1/2 results with relatives and family uptake of BRCA1/2 testing have sampled from predominantly white, high SES cohorts ascertained solely from tertiary care centers. No studies have focused on family communication and testing among relatives of diverse BRCA1/2 carriers. We conducted structured interviews with 73 BRCA1/2 carriers identified at a public hospital and a tertiary cancer center. We asked participants if each first- and second-degree relative was aware of their BRCA1/2 results and whether or not each relative had tested. Generalized estimating equations identified rates and predictors of family communication and testing. Participants disclosed their test results to 73 % of 606 eligible relatives and 31 % of 514 eligible relatives tested. Communication and testing rates were similar for relatives of participants from the public hospital and the tertiary cancer center. Hospital site was not a significant predictor of either result disclosure or relative uptake of testing. African American and Asian/Pacific Islander participants were significantly less likely to disclose their results to their relatives; relatives of African American participants were significantly less likely to test. Addressing these disparities will require further research into the best ways to facilitate family communication and counsel at-risk relatives of racially and socioeconomically diverse BRCA1/2 mutation carriers.
机译:以前的研究检查了BRCA1 / 2结果与亲属之间的交流,以及家庭对BRCA1 / 2测试的接受程度,这些研究主要来自仅由三级护理中心确定的白人,高SES队列。没有研究集中在不同BRCA1 / 2携带者亲属之间的家庭沟通和测试上。我们对在一家公立医院和一家三级癌症中心发现的73例BRCA1 / 2携带者进行了结构化访谈。我们询问参与者,每个一级和二级亲戚是否都知道他们的BRCA1 / 2结果,以及每个亲戚是否都进行了测试。广义估计方程确定了家庭沟通和测试的发生率和预测因素。参与者向606名合格亲戚中的73%和514名合格亲戚中的31%公开了他们的测试结果。公立医院和三级癌症中心参与者的亲属的沟通和检测率相似。医院地点不是结果披露或测试相对采用的重要预测指标。非裔美国人和亚洲/太平洋岛民参与者向他们的亲戚透露他们的结果的可能性大大降低;非裔美国人参与者的亲戚进行测试的可能性大大降低。解决这些差异将需要对促进家庭沟通的最佳方法进行进一步研究,并为种族和社会经济上不同的BRCA1 / 2突变携带者的高危亲属提供法律咨询。

著录项

  • 来源
    《Journal of Genetic Counseling 》 |2013年第5期| 603-612| 共10页
  • 作者单位

    Cancer Risk Program University of California San Francisco">(1);

    University of Michigan Medical School">(2);

    Department of Epidemiology and Biostatistics University of California San Francisco">(3);

    Cancer Risk Program University of California San Francisco">(1);

    Department of Epidemiology and Biostatistics University of California San Francisco">(3);

    Department of Anthropology History and Social Medicine University of California San Francisco">(4);

    Department of Medicine University of California San Francisco">(5);

    University of California San Francisco">(6);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    BRCA1; BRCA2; Hereditary breast and ovarian cancer; Family communication; Family testing; Disparities;

    机译:BRCA1;BRCA2;遗传性乳腺癌和卵巢癌;家庭交流;家庭测试;差距;

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