AI Article Synopsis

  • Employers are starting to include voluntary workplace genomic testing (wGT) in their wellness programs, but there is limited research on its ethical, legal, and social implications (ELSI).
  • Surveying employees at a biomedical research institution showed that 70% preferred wGT in the workplace, significantly higher than preferences for testing via a doctor (54%) or direct-to-consumer options (20%).
  • Most respondents expressed concerns about confidentiality, relevant laws, and privacy, and 92% preferred to understand their test results with the help of a genetic counselor.

Article Abstract

Employers have begun to offer voluntary workplace genomic testing (wGT) as part of employee wellness benefit programs, but few empirical studies have examined the ethical, legal, and social implications (ELSI) of wGT. To better understand employee perspectives on wGT, employees were surveyed at a large biomedical research institution. Survey respondents were presented with three hypothetical scenarios for accessing health-related genomic testing: via (1) their doctor; (2) their workplace; and 3) a commercial direct-to-consumer (DTC) genetic testing company. Overall, 594 employees (28%) responded to the survey. Respondents indicated a preference for genomic testing in the workplace setting (70%; 95% CI 66-74%), followed by doctor's office (54%; 95% CI 50-58%), and DTC testing (20%; 95% CI 17-24%). Prior to participating in wGT, respondents wanted to know about confidentiality of test results (79%), existence of relevant laws and policies (70%), and privacy protection (64%). Across scenarios, 92% of respondents preferred to view the test results with a genetic counselor. These preliminary results suggest that many employees are interested and even prefer genetic testing in the workplace and would prefer testing with support from genetic health professionals. Confirmation in more diverse employer settings will be needed to generalize such findings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010177PMC
http://dx.doi.org/10.3389/fgene.2021.643304DOI Listing

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