Views of Genetic Testing for Autism Among Autism Self-Advocates: A Qualitative Study.

Q1 Arts and Humanities AJOB Empirical Bioethics Pub Date : 2024-04-21 DOI:10.1080/23294515.2024.2336903
R. Klitzman, Ekaterina Bezborodko, Wendy K. Chung, Paul S. Appelbaum
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Abstract

BACKGROUND Autism self-advocates' views regarding genetic tests for autism are important, but critical questions about their perspectives arise. METHODS We interviewed 11 autism self-advocates, recruited through autism self-advocacy websites, for 1 h each. RESULTS Interviewees viewed genetic testing and its potential pros and cons through the lens of their own indiviudal perceived challenges, needs and struggles, especially concerning stigma and discrimination, lack of accommodations and misunderstandings from society about autism, their particular needs for services, and being blamed by others and by themselves for autistic traits. Their views of genetic testing tended not to be binary, but rather depended on how the genetic test results would be used. Interviewees perceived pros of genetic testing both in general and with regard to themselves (e.g., by providing "scientific proof" of autism as a diagnosis and possibly increasing availability of services). But they also perceived disadvantages and limitations of testing (e.g., possible eugenic applications). Participants distinguished between what they felt would be best for themselves and for the autistic community as a whole. When asked if they would undergo testing for themselves, if offered, interviewees added several considerations (e.g., undergoing testing because they support science in general). Interviewees were divided whether a genetic diagnosis would or should reduce self-blame, and several were wary of testing unless treatment, prevention or societal attitudes changed. Weighing these competing pros and cons could be difficult. CONCLUSIONS This study, the first to use in-depth qualitative interviews to assess views of autism self-advocates regarding genetic testing, highlights key complexities. Respondents felt that such testing is neither wholly good or bad in itself, but rather may be acceptable depending on how it is used, and should be employed in beneficial, not harmful ways. These findings have important implications for practice, education of multiple stakeholders, research, and policy.
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自闭症自我倡导者对自闭症基因检测的看法:定性研究。
背景自闭症自我倡导者对自闭症基因检测的看法非常重要,但他们的观点也引发了一些关键问题。方法我们通过自闭症自我倡导网站招募了 11 名自闭症自我倡导者,对他们进行了每人 1 小时的访谈。结果受访者从他们自身感知到的挑战、需求和挣扎的角度来看待基因检测及其潜在的利弊,尤其是关于耻辱和歧视、社会对自闭症缺乏包容和误解、他们对服务的特殊需求以及因自闭症特征而受到他人和自身的指责。他们对基因检测的看法往往不是二元对立的,而是取决于如何使用基因检测结果。受访者普遍认为基因检测对自己有利(例如,提供了自闭症诊断的 "科学证据",并可能增加服务的可获得性)。但他们也看到了检测的缺点和局限性(如可能的优生应用)。参与者将他们认为对自己和对整个自闭症群体最有利的事情区分开来。当被问及如果接受检测,他们是否会为自己接受检测时,受访者补充了一些考虑因素(例如,接受检测是因为他们总体上支持科学)。受访者对基因诊断是否会或应该减少自责意见不一,有几位受访者对检测持谨慎态度, 除非治疗、预防或社会态度有所改变。本研究是首次使用深入的定性访谈来评估自闭症自我倡导者对基因检测的看法,凸显了关键的复杂性。受访者认为,基因检测本身并无好坏之分,而是可以接受的,这取决于基因检测的使用方式,而且基因检测的使用方式应该是有益的,而不是有害的。这些发现对实践、多方利益相关者的教育、研究和政策具有重要意义。
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来源期刊
AJOB Empirical Bioethics
AJOB Empirical Bioethics Arts and Humanities-Philosophy
CiteScore
3.90
自引率
0.00%
发文量
21
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