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Views of Genetic Testing for Autism Among Autism Self-Advocates: A Qualitative Study.
Klitzman, Robert; Bezborodko, Ekaterina; Chung, Wendy K; Appelbaum, Paul S.
Afiliação
  • Klitzman R; Department of Psychiatry, Columbia University, New York, NY, USA.
  • Bezborodko E; Department of Law Ethics and Psychiatry, Columbia University, New York, NY, USA.
  • Chung WK; Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Appelbaum PS; Department of Law Ethics and Psychiatry, NYP Columbia University Irving Medical, New York Presbyterian Hospital, New York, NY, USA.
AJOB Empir Bioeth ; 15(4): 262-279, 2024.
Article em En | MEDLINE | ID: mdl-38643392
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Testes Genéticos / Pesquisa Qualitativa / Estigma Social Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Testes Genéticos / Pesquisa Qualitativa / Estigma Social Idioma: En Ano de publicação: 2024 Tipo de documento: Article