University of Pennsylvania, 3535 Market St, Ste 4100, Philadelphia, PA 19104, USA.
J Clin Oncol. 2011 Nov 10;29(32):4302-6. doi: 10.1200/JCO.2010.33.1561. Epub 2011 Oct 11.
Short-term reactions to BRCA1 and BRCA2 (BRCA1/2) genetic test results have been described in several reports, but the long-terms effects of testing have not been examined extensively.
We conducted an observational study to characterize the long-term impact of genetic testing for BRCA1/2 mutations in 167 women who had received genetic test results at least 4 years ago. We also evaluated the relationship between genetic testing-specific reactions and breast and ovarian cancer screening to determine the behavioral significance of adverse reactions.
Seventy-four percent of women were not experiencing any distress regarding their test result, 41% were not experiencing any uncertainty, and 51% had a score for positive experiences that was suggestive of low levels of adverse reactions in terms of family support and communication. Mutation carriers (odds ratio, 3.96; 95% CI, 1.44 to 10.89; P = .01) were most likely to experience distress. Only less time since disclosure was related significantly to experiencing uncertainty (odds ratio, 0.62; 95% CI, 0.44 to 0.88; P = .008). In terms of cancer screening, 81% of women had a mammogram during the year before study enrollment, 25% had magnetic resonance imaging (MRI), 20% had a transvaginal ultrasound, and 20% had a CA-125. Experiencing distress was associated significantly with having a CA-125 (χ(2) = 3.89, P = .05), and uncertainty was associated with having an MRI (χ(2) = 8.90, P = .003).
Our findings show that women are not likely to experience genetic testing concerns several years after receiving BRCA1/2 test results; distress and uncertainty are not likely to have adverse effects on screening among women at risk for hereditary disease.
已有多项报告描述了 BRCA1 和 BRCA2(BRCA1/2)基因检测结果的短期反应,但尚未广泛研究检测的长期影响。
我们进行了一项观察性研究,以描述 167 名至少在 4 年前接受 BRCA1/2 基因突变检测的女性接受基因检测结果的长期影响。我们还评估了与基因检测相关的反应与乳腺癌和卵巢癌筛查之间的关系,以确定不良反应的行为意义。
74%的女性对检测结果没有任何困扰,41%的女性没有任何不确定性,51%的女性对家庭支持和沟通方面的积极体验有一个评分,这表明她们的不良反应水平较低。突变携带者(比值比,3.96;95%置信区间,1.44 至 10.89;P=.01)最有可能感到困扰。只有披露后时间较短与感到不确定显著相关(比值比,0.62;95%置信区间,0.44 至 0.88;P=.008)。就癌症筛查而言,81%的女性在研究入组前一年进行了乳房 X 线照相术,25%进行了磁共振成像(MRI),20%进行了经阴道超声检查,20%进行了 CA-125 检查。感到困扰与 CA-125 检查显著相关(χ(2) = 3.89,P =.05),而不确定性与 MRI 检查显著相关(χ(2) = 8.90,P =.003)。
我们的研究结果表明,女性在接受 BRCA1/2 检测结果几年后不太可能对基因检测产生担忧;在遗传性疾病风险女性中,困扰和不确定性不太可能对筛查产生不利影响。