Stuttgen Kelsey, Dvoskin Rachel, Bollinger Juli, McCague Allison, Shpritz Barnett, Brandt Jason, Mathews Debra
Berman Institute of Bioethics, Johns Hopkins University, Baltimore, Maryland.
Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Mol Genet Genomic Med. 2018 Nov;6(6):1140-1147. doi: 10.1002/mgg3.494. Epub 2018 Nov 4.
In 1983, Huntington's disease (HD) was the first genetic disease mapped using DNA polymorphisms. Shortly thereafter, presymptomatic genetic testing for HD began in the context of two research studies. One of these trials was at the Johns Hopkins University Huntington's Disease Center.
As part of the protocol, risk perception (RP) values were collected at 16 time points before and after testing. The current study investigated changes in RP scores before and after genetic testing. Of the 186 participants with pre- and post-testing RP values, 39 also had contemporaneous research clinic notes and recent semi-structured interviews available for analysis.
The data reveal tremendous diversity in RP. While the RP scores of most individuals change in the way one would expect, 27% of participants demonstrated unexpected changes in RP after disclosure. A significantly higher proportion of individuals who received an expanded repeat result had unexpected changes in RP, compared with those who received normal repeat results.
The data suggest that individuals' RP is influenced by more than merely the results of genetic testing. This finding is important for genetic counselors and healthcare providers, as it suggests that even comprehensive patient education and disclosure of genetic test results may not ensure that people fully appreciate their disease risk.
1983年,亨廷顿舞蹈症(HD)成为首个利用DNA多态性进行基因定位的遗传疾病。此后不久,针对HD的症状前基因检测在两项研究中展开。其中一项试验在约翰霍普金斯大学亨廷顿舞蹈症中心进行。
作为研究方案的一部分,在检测前后的16个时间点收集风险认知(RP)值。当前研究调查了基因检测前后RP分数的变化。在186名有检测前后RP值的参与者中,39人同时有研究诊所记录和近期半结构化访谈可供分析。
数据显示RP存在巨大差异。虽然大多数人的RP分数变化符合预期,但27%的参与者在结果披露后出现了意外的RP变化。与收到正常重复结果的人相比,收到扩展重复结果的个体出现意外RP变化的比例显著更高。
数据表明,个体的RP不仅仅受基因检测结果的影响。这一发现对遗传咨询师和医疗服务提供者很重要,因为这表明即使进行全面的患者教育并披露基因检测结果,也可能无法确保人们充分认识到自己的疾病风险。