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接受遗传性非息肉病性结直肠癌基因检测的结直肠癌幸存者:动机因素与心理社会功能

Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning.

作者信息

Esplen M J, Madlensky L, Aronson M, Rothenmund H, Gallinger S, Butler K, Toner B, Wong J, Manno M, McLaughlin J

机构信息

Behavioral Sciences and Health Research Division, Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada.

出版信息

Clin Genet. 2007 Nov;72(5):394-401. doi: 10.1111/j.1399-0004.2007.00893.x. Epub 2007 Sep 24.

DOI:10.1111/j.1399-0004.2007.00893.x
PMID:17892499
Abstract

Hereditary non-polyposis colorectal cancer (HNPCC) represents about 1-3% of all cases of colorectal cancer (CRC). The objectives of the study were to examine motivational factors, expectations and psychosocial functioning in a sample of CRC survivors undergoing genetic testing for HNPCC. A cross-sectional survey of 314 colorectal cancer patients recruited through a population-based colon cancer family registry was conducted. Motivations for genetic testing for hereditary cancer were similar to those of clinic-based samples of CRC patients and included learning of the increased risk to offspring and finding out if additional screening was needed. While age at diagnosis and sex were associated with psychological functioning, significant predictors of post-counseling distress were perceived lower satisfaction with social support, an escape-avoidant coping style and the anticipation of becoming depressed if a mutation was present. Most cancer survivors anticipated disclosing test results to relatives and physicians. Cancer survivors reported several motivations for genetic testing for HNPCC that varied by sex. A subgroup of survivors with lower satisfaction with social support and an escape-avoidant coping style were worried about the potential impact of genetic test results and demonstrated more distress following counseling. Findings have implications for future research and potential support needs during the genetic counseling and testing process.

摘要

遗传性非息肉病性结直肠癌(HNPCC)约占所有结直肠癌(CRC)病例的1%-3%。本研究的目的是在接受HNPCC基因检测的CRC幸存者样本中,考察其动机因素、期望和心理社会功能。对通过基于人群的结肠癌家族登记处招募的314例结直肠癌患者进行了横断面调查。遗传性癌症基因检测的动机与基于临床的CRC患者样本相似,包括了解后代患病风险增加以及确定是否需要额外的筛查。虽然诊断年龄和性别与心理功能有关,但咨询后困扰的显著预测因素是对社会支持的满意度较低、逃避应对方式以及如果存在突变则预期会抑郁。大多数癌症幸存者预计会向亲属和医生披露检测结果。癌症幸存者报告了几种HNPCC基因检测的动机,这些动机因性别而异。对社会支持满意度较低且采用逃避应对方式的幸存者亚组担心基因检测结果的潜在影响,并且在咨询后表现出更多困扰。研究结果对未来研究以及基因咨询和检测过程中的潜在支持需求具有启示意义。

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