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Understanding opposition to human gene editing

A role for pathogen disgust sensitivity?

Published online by Cambridge University Press:  18 September 2020

Isaac Halstead*
Affiliation:
Royal Holloway University of London
Gary J. Lewis*
Affiliation:
Royal Holloway University of London
*
Corresponding authors: Isaac Halstead, Royal Holloway University of London, Egham, TW20 0EX, United Kingdom. Email: isaac.halstead.2018@live.rhul.ac.uk; Gary J. Lewis, Royal Holloway University of London, Egham, TW20 0EX, United Kingdom. Email: gary.lewis@rhul.ac.uk.
Corresponding authors: Isaac Halstead, Royal Holloway University of London, Egham, TW20 0EX, United Kingdom. Email: isaac.halstead.2018@live.rhul.ac.uk; Gary J. Lewis, Royal Holloway University of London, Egham, TW20 0EX, United Kingdom. Email: gary.lewis@rhul.ac.uk.

Abstract

Recent advances in gene editing technology promise much for medical advances and human well-being. However, in parallel domains, there have been objections to the use of such biotechnologies. Moreover, the psychological factors that govern the willingness to use gene editing technology have been underexplored to date. In this registered report, we sought to test whether pathogen disgust sensitivity is linked with opposition to gene editing. U.K.-based adult participants (N = 347) were recruited to this study. Gene editing attitudes reflected two largely distinct latent factors concerning enhancing human traits and treating medical disorders. In contrast to prediction, pathogen disgust sensitivity was related to greater support for gene editing in both of these domains. This result suggests that gene editing, at least in the current study, is not viewed as pathogenic, or that the perceived benefits of gene editing outweigh any perceived pathogen risk.

Information

Type
Article
Copyright
© Association for Politics and the Life Sciences 2020
Figure 0

Table 1. Descriptive statistics of study variables.

Figure 1

Table 2. Factor loading results for the gene editing items.

Figure 2

Table 3. Intercorrelations for study variables.

Figure 3

Table 4. Regression model results with opposition to GE-enhancement and GE-treatment as dependent variable.

Figure 4

Table 5. Regression model results with opposition to GM crops and cultured meat as dependent variables.

Figure 5

Table 6. Regression model results with opposition to GE-enhancement and GE-treatment as dependent variables (including core disgust sensitivity as an independent variable).

Figure 6

Table 7. Regression model results with opposition to GM crops and cultured meat as dependent variables (including core disgust sensitivity as an independent variable).

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