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Familial context of genetic testing for cancer susceptibility: Sibling interactions and psychosocial responses.

机译:癌症易感性基因测试的家族背景:兄弟姐妹之间的互动和社会心理反应。

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Mutations in the genes BRCA1 and BRCA2 are associated with increased risks of breast and ovarian cancer, and in recent years genetic testing has been used to identify such mutations. Researchers have theorized that in addition to an individual's test result, the family context may play an important role in psychosocial responses to genetic testing. The present study compared psychological and physiological responses among three types of adult sibling dyads with different combinations of genetic test results: carrier/carrier, carrier/noncarrier, noncarrier/noncarrier. Ninety-eight sibling participants (49 pairs) completed written questionnaires focused on their feelings and behavior toward each other. Seventy of these siblings (35 pairs) participated in structured, interactive sessions with each other.; Results from the study indicated that carrier/noncarrier pairs reported more state anger and less sibling affiliation during the session than carrier/carrier pairs reported. Compared with noncarrier/noncarrier dyads, carrier/noncarrier pairs reported higher levels of dominant support behavior, lower levels of affiliative support behavior, more state anger, more dominant behavior from their sibling during the session, and displayed fewer skin conductance responses. In a third type of contrast between carrier/carrier and noncarrier/noncarrier pairs, carrier/carrier dyads noted significantly more general sibling affiliation, more dominant support behavior, higher levels of dominance from their sibling, and displayed higher heart rates and skin conductance levels. The results of this study indicated that in general, pairs of siblings with opposite test results may respond with more negative perceptions of each other, while pairs in which both siblings are carriers may respond with more positive perceptions. More studies are needed to further delineate the impact of family context on psychosocial responses to genetic testing.
机译:BRCA1和BRCA2基因的突变与乳腺癌和卵巢癌的风险增加相关,并且近年来,基因测试已被用于识别此类突变。研究人员认为,除了个人的测试结果外,家庭背景还可能在对基因测试的社会心理反应中发挥重要作用。本研究比较了三种遗传测试结果不同组合的成年同胞双胞胎的心理和生理反应:携带者/携带者,携带者/非携带者,非携带者/非携带者。 98位兄弟姐妹参与者(49对)完成了针对他们彼此之间的感受和行为的书面问卷。这些兄弟姐妹中有70个(35对)互相参加了结构化的互动会议。研究结果表明,与报告的携带者/携带者对相比,携带者/非携带者对在会议期间报告了更多的国家愤怒和更少的兄弟姐妹关系。与非携带者/非携带者双性恋相比,携带者/非携带者对报告了较高水平的支配支持行为,较低水平的附属支持行为,更多的国家愤怒,在会话期间来自其兄弟姐妹的更多支配行为,并且显示出较少的皮肤电导反应。在承运人/承运人和非承运人/非承运人对之间的第三种对比中,承运人/承运人二元组注意到更普遍的兄弟姐妹关系,更显着的支持行为,来自其兄弟姐妹的更高水平的统治力,以及更高的心率和皮肤电导水平。这项研究的结果表明,总体而言,测试结果相反的兄弟姐妹对彼此的负面看法可能会做出更多的回应,而两个兄弟姐妹都是携带者的兄弟姐妹对可能会做出更加正面的看法。需要进行更多的研究以进一步描述家庭背景对基因测试的社会心理反应的影响。

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