Abstract

The interpretation of genetic information in clinical settings raises moral issues about adequate risk communication and individual responsibility about one’s health behavior. However, it is not well-known what role numeric probabilities and/or the conception of disease and genetics play in the lay understanding of predictive genetic diagnostics. This is an important question because lay understanding of genetic risk information might have particular implications for self-responsibility of the patients.Aim: Analysis of lay attitudes and risk perceptions of German lay people on genetic testing with a special focus on how they deal with the numerical information.Methods: We conducted and analyzed seven focus group discussions (FG) with lay people (n = 43).Results: Our participants showed a positive attitude toward predictive genetic testing. We identified four main topics: (1) Anumeric risk instead of statistical information; (2) Treatment options as a factor for risk evaluation; (3) Epistemic and aleatory uncertainty as moral criticism; (4) Ambivalence as a sign of uncertainty.Conclusion: For lay people, risk information, including the statistical numeric part, is perceived as highly normatively charged, often as an emotionally significant threat. It seems necessary to provide lay people with a deeper understanding of risk information and of the limitations of genetic knowledge with respect to one’s own health responsibility.

Highlights

  • Technological progress over the recent years has led to an unprecedented increase in speed and precision of genetic testing

  • Our participants showed a positive attitude toward predictive genetic testing

  • The focus group discussions (FG) guideline consisted of four realistic main scenarios, including predictive genetic testing for breast cancer (BC) and early-onset Alzheimer’s disease (AD), biomarker research for stratification in neo-adjuvant colon cancer (CoC) therapy and the possibility of DTC direct-to-consumer genetic testing (GT), and whole genome sequencing (WGS)

Read more

Summary

Introduction

Technological progress over the recent years has led to an unprecedented increase in speed and precision of genetic testing. Current studies have examined challenges for lay people in dealing with risk information from genetic testing (Engelhardt et al, 2017; Han et al, 2017; Solomon et al, 2017).1 They showed that perceived risk is an important subjective psychological phenomenon that is closely intertwined with individual judgments about susceptibility to getting ill as well as potential benefits from interventions (Weinstein and Klein, 1995). Important ethical issues remain unsolved, such as how to ensure the right not to know, how to consider different models of informed consent in light of the predictive, probabilistic character of genetic risk information, or how to balance the interests of a person with the interests of their genetic relatives (Andorno, 2004; Beskow and Burke, 2010; Borry et al, 2014; Leefmann et al, 2017; Falahee et al, 2018; Inthorn, 2018) For lay people, these ethical issues complicate decision-making, since conflicting interests may occur in genetic testing. There is a variety of general literature about risk and uncertainty in the context of medical decision-making and genetic testing, and how

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call