评估远程医疗癌症遗传学计划的有效性:BRCA 试点研究。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Esther Rose, Melanie Walker Hardy, Rachael Gates, Christine Stanislaw, Jane Meisel, Karen Arnovitz Grinzaid
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引用次数: 0

摘要

简介阿什肯纳兹犹太人(AJ)的 BRCA 基因突变风险为 40 分之 1(2.5%),是普通人群风险的 10 倍。JScreen 发起了 "PEACH BRCA 研究",这是一个基于远程医疗的 BRCA 教育和检测平台,目标是为不符合国家检测标准的低风险 AJ 人创建一个有效的 BRCA 检测模式。其他目标还包括确定该群体的 BRCA 基因突变率,评估仅对 3 种常见 AJ 基因创始人突变进行筛查的充分性,以及评估对远程医疗模式的满意度,以便为在全国范围内启动更广泛的癌症基因检测计划提供信息:参与标准包括:AJ、居住在亚特兰大市区、年龄在 25 岁及以上、无 BRCA 相关癌症的个人或近亲病史。通过视频和书面总结提供测试前教育,随后提供免费 BRCA1/2 测序和测试后遗传咨询。参与者对测试前和测试后的调查进行了回复,以评估知识和满意度。那些没有资格参加测试的人将收到遗传咨询资源,随后再接受调查:51 名参与者接受了检测,结果包括 4 例阳性(阳性率为 0.8%)、494 例阴性和 3 例意义不确定的变异。对研究过程的总体满意度很高(96.9/100),对 BRCA 的了解程度很高(97.5% 的参与者通过了检测前的知识测验),对检测前后的教育满意度也很高(97.9% 的参与者对检测前的视频和书面总结表示满意,99.5% 的参与者认为检测后的遗传咨询课程很有价值)。许多参与者表示有兴趣接受更广泛的癌症检测:结论:在低风险 AJ 群体中,BRCA 基因创始人突变率明显低于之前确定的 AJ 40 分之 1 的比率。研究还确定,癌症遗传学项目的远程医疗模式是有效的,并能为受测人群所接受。这项研究确立了通过远程医疗平台进行更广泛的癌症基因检测的兴趣,并表明,只要充分纳入患者教育和遗传咨询,在全国范围内的犹太社区和其他人群中进行检测可能会取得成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A BRCA Pilot Study.

Introduction: Ashkenazi Jewish (AJ) individuals face a 1 in 40 (2.5%) risk of having a BRCA mutation, which is 10 times the general population risk. JScreen launched the PEACH BRCA Study, a telehealth-based platform for BRCA education and testing, with the goal of creating an effective model for BRCA testing in low-risk AJ individuals who do not meet national testing criteria. Other goals were to determine the rate of BRCA mutations in this group, to assess the adequacy of screening for the 3 common AJ founder mutations only, and to assess satisfaction with the telehealth model to help inform a national launch of a broader cancer genetic testing program.

Methods: Criteria for participation included those who were AJ, resided in the metro-Atlanta area, were aged 25 and older, and had no personal or close family history of BRCA-related cancers. Pre-test education was provided through a video and written summary, followed by complimentary BRCA1/2 sequencing and post-test genetic counseling. Participants responded to pre- and post-test surveys, which assessed knowledge and satisfaction. Those who were not eligible to participate were sent genetic counseling resources and later surveyed.

Results: Five hundred one participants were tested and the results included 4 positives (0.8% positivity rate), 494 negatives, and 3 variants of uncertain significance. Overall satisfaction with the study process was high (96.9/100), knowledge about BRCA was high (97.5% of participants passed a pre-test knowledge quiz), and satisfaction with pre- and post-test education was high (97.9% of participants were satisfied with the pre-test video and written summary, and 99.5% felt that their post-test genetic counseling session was valuable). Many participants expressed interest in receiving broader cancer testing.

Conclusions: The BRCA founder mutation rate in a low-risk AJ population was significantly lower than the previously established AJ rate of 1 in 40. It was also determined that a telehealth model for a cancer genetics program is effective and acceptable to the population tested. This study established interest in broader cancer genetic testing through a telehealth platform and suggested that testing may be successful in the Jewish community at a national level and potentially in other populations, provided that patient education and genetic counseling are adequately incorporated.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
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