Analogies in Genomics Policymaking: Debates and Drawbacks

Am J Hum Genet. 2020 Nov 5;107(5):797-801. doi: 10.1016/j.ajhg.2020.08.024.

Abstract

The analogy between genomics and imaging has been an important touchstone in the debate on how secondary findings should be handled in both clinical and research genomics contexts. However, a critical eye is needed to understand whether an analogy like this one provides an adequate basis for policymaking in genomics. Genomics and imaging are undoubtedly similar in certain ways, but whether that similarity is adequate to justify adopting identical policies is a task that requires further analysis. This is highlighted by the fact that secondary findings are produced in other domains of medicine and public health, such as newborn screening programs, routine laboratory panels, and antibiotic sensitivity testing, and that the practices for handling secondary findings in each of these areas are different. These examples demonstrate that medicine has no single comprehensive policy or set of practices for managing secondary findings. Analogies to imaging, newborn screening, routine testing panels, and antibiotic sensitivity testing all lead to different policy options for genomics. In this piece we argue that analogies are a powerful way of driving policy discussions by rendering two different areas of medical practice similar, but an overdependence on a single analogy risks limiting policy discussions in potentially deleterious ways.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Diagnostic Imaging / ethics
  • Disclosure / ethics*
  • Disclosure / legislation & jurisprudence
  • Genetic Testing / ethics*
  • Genetic Testing / legislation & jurisprudence
  • Genomics / ethics*
  • Genomics / legislation & jurisprudence
  • Health Policy / legislation & jurisprudence*
  • Humans
  • Incidental Findings
  • Infant, Newborn
  • Policy Making*
  • Public Health / ethics*
  • Sequence Analysis, DNA