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Preferences for genetic testing for colorectal cancer within a population-based screening program: a discrete choice experiment

Authors :
Veldwijk, Jorien
Lambooij, Mattijs S
Kallenberg, Frank G J
van Kranen, Henk J
Bredenoord, Annelien L
Dekker, Evelien
Smit, Henriëtte A
de Wit, G Ardine
Source :
European Journal of Human Genetics: EJHG; March 2016, Vol. 24 Issue: 3 p361-366, 6p
Publication Year :
2016

Abstract

This study explored individuals’ preferences for genetic testing for colorectal cancer (CRC) in a screening situation and their willingness to participate in genetic testing for Lynch syndrome, familial adenomatous polyposis (FAP), and familial colorectal cancer (FCC). For that purpose, 532 respondents aged 55–65 years completed a Discrete Choice Experiment. Using panel latent class models, the preferences for two screening situation characteristics (the probability of being genetically predisposed and the probability of developing CRC) and screening test characteristics (the frequency of preventive colonoscopies and CRC survival) were estimated. Based on these preferences, respondents’ willingness to participate in the three screening initiatives was estimated. Lower-educated respondents and respondents who express serious anxiety and worries found colonoscopy frequency and the probability of developing CRC relatively more important and survival relatively less important compared with higher-educated respondents and respondents who express no anxiety and worries. These differences in preferences resulted in opposite preferences for participation in FCC and FAP screening. In conclusion, the general population is willing to participate in genetic screening for CRC. If individuals are suspected of genetic or familial CRC, they should at least be informed about their increased risk of being genetically predisposed and about the importance of participating in all preventive follow-up colonoscopies in order to maximize survival.

Details

Language :
English
ISSN :
10184813 and 14765438
Volume :
24
Issue :
3
Database :
Supplemental Index
Journal :
European Journal of Human Genetics: EJHG
Publication Type :
Periodical
Accession number :
ejs38050761
Full Text :
https://doi.org/10.1038/ejhg.2015.117