Division of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Center for Precision Medicine and Genomics, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
J Genet Couns. 2021 Jun;30(3):742-754. doi: 10.1002/jgc4.1364. Epub 2020 Dec 26.
With the broader introduction of genomic medicine in research and clinical care, an increasing number of persons are offered genetic testing. Many factors, including genetic literacy, may impact the utilization of genetic results by patients and their families. We developed a rapid, self-administered measure of genetic literacy, called Genetic Literacy Fast Test (GeneLiFT). We next evaluated the association of GeneLiFT scores with the comprehension of limitations of genomic medicine in participants undergoing genetic testing in the NIH-sponsored eMERGE III study at Columbia University Irving Medical Center, New York. All participants underwent genetic screening for variants in 74 actionable genes associated with adult-onset disorders. A diverse cohort of 724 participants completed the survey (60% women, 45% less than 40 years old, and 53% self-reported White non-Hispanic ancestry). The GeneLiFT was validated using known group differences based on education, health literacy, and numeracy, and with questions assessing genetic knowledge. GeneLiFT identified multiple standard genetics terms, that is, jargon, not recognized by more than 50% of participants (including actionability and pathogenicity). Low genetic literacy, identified in 210 participants (29%), was significantly associated with poor understanding of the limitations of genetic testing (p-values < 10 ). This association was independent of education, health literacy, and numeracy levels, highlighting the importance of directly measuring genetic literacy. Low genetic literacy was also associated with low satisfaction with the informed consent process. GeneLiFT is a practical tool for rapid assessment of genetic literacy in large studies or clinical care. GeneLiFT will allow future research to efficiently assess the role of genetic literacy on the clinical impact of genetic testing.
随着基因组医学在研究和临床护理中的广泛应用,越来越多的人接受基因检测。许多因素,包括遗传素养,可能会影响患者及其家属对遗传结果的利用。我们开发了一种快速的、自我管理的遗传素养衡量工具,称为遗传素养快速测试(GeneLiFT)。接下来,我们评估了 GeneLiFT 评分与在哥伦比亚大学欧文医学中心 NIH 赞助的 eMERGE III 研究中接受基因检测的参与者对基因组医学局限性的理解之间的关联。所有参与者都接受了 74 个与成人发病障碍相关的可操作基因变异的基因筛查。一个多元化的 724 名参与者完成了调查(60%为女性,45%年龄小于 40 岁,53%自我报告为白种非西班牙裔血统)。GeneLiFT 通过基于教育、健康素养和计算能力的已知组差异以及评估遗传知识的问题进行了验证。GeneLiFT 识别了多个标准遗传术语,即超过 50%的参与者不认识的行话(包括可操作性和致病性)。210 名参与者(29%)的遗传素养低,与对基因检测局限性的理解较差显著相关(p 值 < 10)。这种关联独立于教育、健康素养和计算能力水平,突出了直接衡量遗传素养的重要性。遗传素养低也与对知情同意过程的满意度低有关。GeneLiFT 是一种在大型研究或临床护理中快速评估遗传素养的实用工具。GeneLiFT 将允许未来的研究有效地评估遗传素养对基因检测临床影响的作用。