Gene therapy: perspectives from young adults with Leber’s congenital amaurosis

Aims/purpose To investigate Leber congenital amaurosis (LCA) patients’ expectations, decision-making processes and gene therapy-related concerns. Methods Using a qualitative approach, we explored perceptions of gene therapy and clinical trials among individuals with LCA. Young adults with a clinical...

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Published inEye (London) Vol. 36; no. 11; pp. 2088 - 2093
Main Authors Napier, Melanie P., Selvan, Kavin, Hayeems, Robin Z., Shuman, Cheryl, Chitayat, David, Sutherland, Joanne E., Day, Megan A., Héon, Elise
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.11.2022
Nature Publishing Group
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Summary:Aims/purpose To investigate Leber congenital amaurosis (LCA) patients’ expectations, decision-making processes and gene therapy-related concerns. Methods Using a qualitative approach, we explored perceptions of gene therapy and clinical trials among individuals with LCA. Young adults with a clinical diagnosis of LCA were recruited through the Ocular Genetics Programme at the Hospital for Sick Children. Semi-structured interviews were conducted with ten patients and analysed following the principles of qualitative description. Results Study participants were aware of ongoing gene therapy research trials and actively sought information regarding advances in ophthalmology and vision restoration. The majority of participants would enrol or were enrolled in a gene-replacement therapy trial, while a minority was ambivalent or would not enrol if provided an opportunity. Participants attributed different values to clinical trials, which influenced their willingness to participate. Intrinsic factors related to coping, adaptation to vision loss and resilience also influenced decision-making. Discussion This study highlights the complex factors involved in gene-therapy-related decision-making and acts as a proponent for adopting patient-centred care strategies when counselling individuals considering gene therapy or clinical trial participation.
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ISSN:0950-222X
1476-5454
DOI:10.1038/s41433-021-01763-z