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Australians' views on personal genomic testing: focus group findings from the Genioz study.
Metcalfe, Sylvia A; Hickerton, Chriselle; Savard, Jacqueline; Terrill, Bronwyn; Turbitt, Erin; Gaff, Clara; Gray, Kathleen; Middleton, Anna; Wilson, Brenda; Newson, Ainsley J.
Affiliation
  • Metcalfe SA; Department of Paediatrics, The University of Melbourne, Melbourne, Australia. sylvia.metcalfe@mcri.edu.au.
  • Hickerton C; Genetics Education and Health Research, Murdoch Children's Research Institute, Melbourne, Australia. sylvia.metcalfe@mcri.edu.au.
  • Savard J; Genetics Education and Health Research, Murdoch Children's Research Institute, Melbourne, Australia.
  • Terrill B; Sydney Health Ethics, Sydney School of Public Health, The University of Sydney, Sydney, Australia.
  • Turbitt E; Garvan Institute of Medical Research, Sydney, Australia.
  • Gaff C; Garvan Institute of Medical Research, Sydney, Australia.
  • Gray K; Genome.One, Sydney, Australia.
  • Middleton A; St Vincent's Clinical School, University NSW, Sydney, Australia.
  • Wilson B; Department of Paediatrics, The University of Melbourne, Melbourne, Australia.
  • Newson AJ; Genetics Education and Health Research, Murdoch Children's Research Institute, Melbourne, Australia.
Eur J Hum Genet ; 26(8): 1101-1112, 2018 08.
Article in En | MEDLINE | ID: mdl-29706641
ABSTRACT
Personal genomic testing provides healthy individuals with access to information about their genetic makeup for purposes including ancestry, paternity, sporting ability and health. Such tests are available commercially and globally, with accessibility expected to continue to grow, including in Australia; yet little is known of the views/expectations of Australians. Focus groups were conducted within a multi-stage, cross-disciplinary project (Genioz) to explore this. In mid-2015, 56 members of the public participated in seven focus groups, allocated into three age groups 18-24, 25-49, and ≥50 years. Three researchers coded transcripts independently and generated themes. Awareness of personal genomic testing was low, but most could deduce what "personal genomics" might entail. Very few had heard of the term "direct-to-consumer" testing, which has implications for organisations developing information to support individuals in their decision-making. Participants' understanding of genetics was varied and drawn from several sources. There were diverse perceptions of the relative influence of genetics and environment on health, mental health, behavior, talent, or personality. Views about having a personal genomic test were mixed, with greater interest in health-related tests if they believed there was a reason for doing so. However, many expressed scepticisms about the types of tests available, and how the information might be used; concerns were also raised about privacy and the potential for discrimination. These exploratory findings inform subsequent stages of the Genioz study, thereby contributing to strategies of supporting Australians to understand and make meaningful and well-considered decisions about the benefits, harms, and implications of personal genomic tests.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attitude / Genetic Testing / Direct-To-Consumer Screening and Testing Type of study: Diagnostic_studies / Prognostic_studies / Qualitative_research Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attitude / Genetic Testing / Direct-To-Consumer Screening and Testing Type of study: Diagnostic_studies / Prognostic_studies / Qualitative_research Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Australia