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因种系 CDKN2A 变异而接受黑色素瘤和胰腺癌风险增加监测的个体的心理社会问题:一项焦点小组研究。

Psychosocial issues of individuals undergoing surveillance for increased risk of melanoma and pancreatic cancer due to a germline CDKN2A variant: A focus group study.

机构信息

Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Medical Psychology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

J Genet Couns. 2024 Oct;33(5):1059-1069. doi: 10.1002/jgc4.1820. Epub 2023 Oct 25.

Abstract

Individuals with a germline CDKN2A pathogenic variant (PV) are at high risk of developing melanoma and pancreatic cancer and are therefore offered surveillance. The potential advantages and disadvantages associated with genetic testing and surveillance are discussed during medical counseling, although little is known about the associated psychosocial factors that are relevant to this population. This study sought to provide a qualitative exploration of psychosocial factors related to genetic testing and participation in skin and pancreatic surveillance in (potential) carriers of a CDKN2A PV. Fifteen individuals-both at-risk individuals and confirmed variant carriers-participated in one of the three online focus groups. Pre-defined discussion topics, including genetic testing, cancer surveillance, influence on lifestyle and family planning, were discussed. Patients reported that important reasons to engage in genetic testing included the possibility to participate in surveillance to gain control over their cancer risk and to get clarification on the potential carrier status of their children. We observed considerable differences in risk perception and experienced burden of surveillance. Knowledge of the PV has had a positive influence on lifestyle factors and altered attitudes toward life in some. Most participants were not aware of preimplantation genetic testing. This focus group study provided insight into a variety of psychosocial themes related to (potential) carriership of a CDKN2A PV. Future efforts should focus on identifying those who may benefit from additional psychosocial support, development of a centralized source of information, and assessing the knowledge, needs, and timing of counseling for family planning.

摘要

个体携带种系 CDKN2A 致病性变异(PV),患黑色素瘤和胰腺癌的风险很高,因此需要进行监测。在医学咨询中会讨论与基因检测和监测相关的潜在优缺点,但对于与该人群相关的、重要的心理社会因素却知之甚少。本研究旨在定性探讨与 CDKN2A PV 携带者的基因检测和皮肤及胰腺监测参与相关的心理社会因素。15 名个体(包括高风险个体和已确诊变异携带者)参加了三个在线焦点小组中的一个。讨论了预先确定的讨论主题,包括基因检测、癌症监测、对生活方式和计划生育的影响。患者报告说,参与基因检测的重要原因包括参与监测的可能性,以获得对癌症风险的控制,并明确子女的潜在携带者身份。我们观察到风险感知和监测负担存在显著差异。对 PV 的了解对一些人的生活方式因素产生了积极影响,并改变了他们对生活的态度。大多数参与者不知道胚胎植入前基因检测。本焦点小组研究深入了解了与 CDKN2A PV 携带者(潜在)相关的多种心理社会主题。未来的研究应侧重于确定那些可能需要额外心理社会支持的人群,开发集中的信息来源,并评估咨询的知识、需求和时机,以进行计划生育。

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