The FDA authorization of direct-to-consumer genetic testing for three BRCA1/2 pathogenic variants: A twitter analysis of the public's response

7Citations
Citations of this article
22Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Objectives: In March 2018, the Food and Drug Administration (FDA) announced its authorization of a direct-to-consumer (DTC) genetic test for three pathogenic BRCA1/2 variants. We sought to determine to whether social media discussion increased following the authorization, who was driving social media conversations, and what topics were discussed. Methods: Using Crimson Hexagon, we described tweets before, during, and after the FDA announcement authorizing 23andMe to return BRCA1/2 results (3/4/18-3/10/18). We conducted qualitative coding of a subset of 605 tweets to better understand Twitter communication. Results: We identified 11 055 twitter posts across the week of FDA's announcement. Twitter discourse about 23andMe and the FDA authorization peaked the day following the FDA's press release. Most tweets (48.6%) were informational and 26.3% were either expressing opinions (about 23andMe and/or FDA authorization, 14.9%) or testimonials (personal experiences with genetic testing, 11.4%). The types of tweets varied over the week-long period (P

Cite

CITATION STYLE

APA

Roberts, M. C., Allen, C. G., & Andersen, B. L. (2019). The FDA authorization of direct-to-consumer genetic testing for three BRCA1/2 pathogenic variants: A twitter analysis of the public’s response. JAMIA Open, 2(4), 411–415. https://doi.org/10.1093/jamiaopen/ooz037

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free