公众对披露家庭遗传风险的态度:一项对葡萄牙一般人口样本的调查

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY
Iara Ribeiro , João Tavares , Liliana Sousa , Álvaro Mendes
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引用次数: 0

摘要

遗传和基因组检测通常不仅对被检测个体有影响,而且对其遗传亲属也有影响。本研究旨在描述公众对家族遗传风险披露的态度。一项在线调查由葡萄牙普通人口样本(n = 1034)完成,评估对基因检测的偏好、遗传风险信息的接收以及与家庭成员分享这些信息。结果显示,受访者强烈倾向于接受有关遗传风险的信息并进行基因检测。也有充分的共识认为,家庭成员应该被告知发展遗传疾病的风险,并进行基因检测。此外,参与者表示更倾向于医疗保健专业人员告知他们自己和他们的家庭成员的遗传风险。我们的研究结果表明,人们广泛接受医疗保健介导的家庭成员遗传风险披露的可能性。然而,这种披露方法值得进一步调查,因为与患者亲属的直接接触仍然是一个有争议的问题。考虑到所有关键利益相关者的观点,需要就如何最好地将相关遗传信息级联到患者的家庭成员进行广泛的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Public attitudes towards disclosure of genetic risk in the family: A survey in a sample of the Portuguese general population
Genetic and genomic testing often have implications not only for the individual tested but also for their genetic relatives. This study aims to characterize public attitudes toward the familial disclosure of genetic risks. An online survey was completed by a sample of the Portuguese general population (n = 1034), assessing preferences for genetic testing, the receipt of genetic risk information, and the sharing of such information with family members. Results reveal a strong preference among respondents for receiving information on genetic risks and undergoing genetic testing. There was also ample agreement that family members should be informed about the risk of developing an inherited condition and undergo genetic testing. Additionally, participants expressed a preference for healthcare professionals to inform both themselves and their family members of genetic risks. Our findings suggest broad acceptance of the possibility for healthcare-mediated disclosure of genetic risks to family members. However, this approach to disclosure warrants further investigation, as direct contact with patients' relatives remains a contentious issue. A broad discussion is needed on how to best cascade relevant genetic information to patients' family members, taking into account the perspectives of all key stakeholders.
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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