癌症预防的风险沟通与前景--一项探索性研究,探讨美国中西部非裔美国人和拉美裔美国人对癌症相关基因咨询和检测的看法。

IF 1.5 Q4 GENETICS & HEREDITY
Journal of Community Genetics Pub Date : 2023-04-01 Epub Date: 2023-03-17 DOI:10.1007/s12687-022-00629-5
Crystal Y Lumpkins, Rafaela Nelson, Zawadi Twizele, Mariana Ramírez, Kim S Kimminau, Alisdair Philp, Reem A Mustafa, Andrew K Godwin
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引用次数: 0

摘要

与美国总人口相比,非裔美国人(AA)和拉丁裔美国人在癌症发病率和死亡率方面受到的影响尤为严重。导致这些发病率的原因是影响男性和女性的多种遗传性癌症。其中一些疾病可通过遗传咨询和种系 DNA 检测发现;然而,非裔美国人和拉美裔美国人对这些服务和技术并不了解,所知有限,因此对这些服务和技术的利用严重不足。受多种因素的影响,检测接受检测的影响因素的研究也进展缓慢。研究小组采用了社区参与式研究 (CBPR) 方法,并与由癌症幸存者和共同幸存者组成的社区咨询委员会合作设计了这项探索性研究。研究小组与自称有癌症风险的非裔美国人和拉丁裔美国人(N = 53)进行了六次焦点小组讨论。研究为期 2 个月,探讨了人们对癌症风险的态度、看法和信念,以及对癌症相关遗传咨询和检测风险交流的偏好。出现的主题包括:(1) 对癌症相关基因咨询和检测缺乏了解;(2) 人们经常害怕癌症;(3) 认为癌症相关基因检测可以提供帮助,但也认为不必要的检测会使个人受到医疗伤害;(4) 认为检测对医务人员有利,但对病人不利。本研究的启示提供了一个独特的视角,以探索 AA 族和拉丁裔的生活经验如何为癌症相关基因咨询和检测的战略风险沟通提供信息,并帮助促进癌症健康公平。参与者认为癌症基因检测是重要的癌症风险预防策略。需要与社区成员合作,确定他们对癌症风险以及癌症相关基因咨询和检测的看法,以加强在这些人群中的宣传工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Communicating risk and the landscape of cancer prevention - an exploratory study that examines perceptions of cancer-related genetic counseling and testing among African Americans and Latinos in the Midwest.

African American (AA) and Latino populations are impacted disproportionately by cancer incidence and mortality compared to the general US population. Contributing to these rates are multiple inheritable cancers that impact both men and women. Some of these diseases may be detected through genetic counseling and germline DNA testing; however, AA and Latinos are unaware and have limited knowledge and thus significantly underutilize these services and technologies. Research to detect influencing factors to testing uptake has also been slow due to multiple factors. The research team followed a community-based participatory research (CBPR) approach and worked with a Community Advisory Board composed of cancer survivors and co-survivors to design the exploratory study. Six focus groups were held with a pilot sample of African Americans and Latinos who self-reported to be at-risk for cancer (N = 53). The study was held over a 2-month period where attitudes, perceptions, and beliefs about cancer risk and preference regarding cancer-related genetic counseling and testing risk communication were explored. Themes that emerged included (1) the lack of knowledge about cancer-related genetic counseling and testing; (2) cancer is feared often; (3) cancer-related genetic testing was perceived as something that could help but was also perceived as unnecessary testing that exposed individuals to medical harm; and (4) benefits to test were perceived as favorable for medical personnel but not for the patient. Implications of the study provide a unique lens to explore how lived experiences among AA and Latinos may inform strategic risk communication about cancer-related genetic counseling and testing and help advance cancer health equity. Participants viewed cancer genetic testing as important cancer risk prevention strategies. Identification of perceptions of cancer risk and cancer-related genetic counseling and testing in collaboration with members of the community is needed to bolster communication efforts among these populations.

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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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