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Colorectal Cancer Cases and Relatives of Cases Indicate Similar Willingness to Receive and Disclose Genetic Information

机译:结直肠癌病例及其亲属表明相似的接收和披露遗传信息的意愿

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摘要

Context: Recent developments in genetic testing allow us to detect individuals with inherited susceptibility to some cancers. Genetic testing to identify carriers of cancer-related mutations may help lower risk by encouraging preventive behaviors and surveillance. This study assessed willingness of colon cancer cases and relatives to receive genetic information that may indicate an increased risk for cancer, to whom they would disclose genetic information, and whether receiving genetic test results may influence future prevention behaviors among individuals enrolled in the Seattle Colorectal Cancer Family Registry. Methods: Incident invasive colorectal cancer cases were identified from the Puget Sound Surveillance Epidemiology and End Results (SEER) registry. In 2007, a sequential sample of cases and relatives (n = 147) were asked to respond to a questionnaire addressing study aims. The questionnaire was administered during a baseline or 5-year follow-up interview. Results: Patterns of response to each statement were similar between colorectal cancer cases and relatives. Both colorectal cases (95%) and relatives (95%) reported willingness to receive genetic information. Nearly all participants would tell their doctor the results of a genetic test (99% of cases; 98% of relatives), and all married participants would tell their spouses. Cases (96%) anticipated being slightly more likely than relatives (90%) to change their cancer screening behavior, but this difference was not statistically significant (p = 0.33). Conclusions: A high percentage of both colorectal cancer cases and relatives sampled from the Seattle Colorectal Cancer Family Registry are interested in identifying their genetic status, discussing their genetic status with their family and doctor, and adopting behavioral changes that may reduce cancer risk.
机译:背景:基因检测的最新发展使我们能够检测出对某些癌症具有遗传易感性的个体。通过鼓励预防行为和监测,进行基因检测以鉴定癌症相关突变的携带者可能有助于降低风险。这项研究评估了结肠癌病例和亲属接收可能表明癌症风险增加的遗传信息的意愿,他们将向谁披露遗传信息,以及接受遗传检测结果是否会影响西雅图结直肠癌患者的未来预防行为户籍。方法:从普吉特声音监测流行病学和最终结果(SEER)注册表中识别出事件性侵袭性大肠癌病例。 2007年,要求按顺序抽取病例和亲属(n = 147)来回答针对研究目的的问卷。该调查表是在基线或5年的随访访问中进行的。结果:大肠癌病例与亲属对每种陈述的反应方式相似。大肠癌病例(95%)和亲戚病例(95%)均报告愿意接受遗传信息。几乎所有参与者都将基因测试的结果告诉医生(99%的病例; 98%的亲戚),所有已婚参与者都会告诉其配偶。预期病例(96%)比亲属(90%)更有可能改变其癌症筛查行为,但这种差异在统计学上并不显着(p = 0.33)。结论:从西雅图大肠癌家庭登记处采样的大肠癌病例和亲属中,有很大比例对确定其遗传状况,与家人和医生讨论其遗传状况以及采取可能降低癌症风险的行为改变感兴趣。

著录项

  • 来源
    《Genetic Testing》 |2008年第3期|p.415-420|共6页
  • 作者单位

    Rachel M. CeballosSchool of Public Health and Community Medicine, University of Washington, Seattle, Washington.Polly A. NewcombSchool of Public Health and Community Medicine, University of Washington, Seattle, Washington.Cancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.Jeannette M. BeasleyJohns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.Scot PetersonCancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.Allyson TempletonCancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.Julie R. HuntCancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, Washington;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Colorectal Cancer Cases , Relatives;

    机译:大肠癌病例;
  • 入库时间 2022-08-17 23:43:49

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