Autistic perspectives on the moral and ethical considerations of genetic testing for autism

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mitch Hendry, Loryn Byres, Jehannine Austin
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Abstract

This study aimed to characterize the nuanced perspectives expressed by Autistic adults about genetic testing for autism. In this secondary analysis of an existing dataset, we used inductive content analysis of free-text responses that Autistic adults wrote in response to questions asking about perceptions of genetic testing for autism that had been included in a previous survey. Participants who completed the survey had been recruited online. Three-hundred eighty-nine participants wrote a total of 28,774 words in response to the questions of interest. While some respondents wrote about potential benefits of genetic testing (79/389), more (333/389) wrote about potential negative outcomes of genetic testing. Participants wrote about concerns of eugenics (281/389), described a lack of trust in how genetics information would be used (125/389), and raised concerns that genetic testing could increase discrimination (66/389). This is the largest study to date to conduct an in-depth analysis of Autistic adults’ opinions on genetic testing for autism. Most respondents raised serious concerns. Additional work is needed to collect more Autistic opinions about genetic testing for autism.

Abstract Image

从自闭症角度看自闭症基因检测的道德和伦理考虑。
本研究旨在描述自闭症成年人对自闭症基因检测的微妙观点。在对现有数据集的二次分析中,我们对自由文本回复进行了归纳内容分析,这些回复是自闭症成年人在回答有关自闭症基因检测的看法的问题时所写的,这些问题已经包含在之前的调查中。完成调查的参与者是在网上招募的。389名参与者在回答感兴趣的问题时总共写了28,774个单词。虽然一些受访者写了基因检测的潜在好处(79/389),但更多的受访者(333/389)写了基因检测的潜在负面结果。参与者写了关于优生学的担忧(281/389),描述了对如何使用遗传信息缺乏信任(125/389),并提出了对基因检测可能增加歧视的担忧(66/389)。这是迄今为止规模最大的一项深入分析自闭症成年人对自闭症基因检测意见的研究。大多数受访者都提出了严重的担忧。需要做更多的工作来收集更多关于自闭症基因检测的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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