Choosing not to know: accounts of non-engagement with pre-symptomatic testing for Machado-Joseph disease.
Journal
European journal of human genetics : EJHG
ISSN: 1476-5438
Titre abrégé: Eur J Hum Genet
Pays: England
ID NLM: 9302235
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
11
04
2018
accepted:
22
11
2018
revised:
09
11
2018
pubmed:
24
12
2018
medline:
21
5
2019
entrez:
22
12
2018
Statut:
ppublish
Résumé
This paper reports accounts from people at-risk for, or affected by, Machado-Joseph disease, and their family members, about their decisions not to seek pre-symptomatic testing, therefore remaining (for the time) uninformed about their genetic status. We draw on individual and family semi-structured interviews with participants recruited through a national patient's association (n = 25). Qualitative thematic analysis revealed three main categories of accounts: (1) justifying the decision "not to know", because either no clinical benefit was expected or predictive knowledge was anticipated as psychologically burdensome; (2) prioritizing everyday life, maintaining hope and the goal of living a valid life; and (3) the wish to know: ambivalence and conflict within the family. Findings suggest the value of genetic information is often questioned when no effective treatment or cure is available; and that people have different tolerance thresholds for predictive information, and this impacts individuals within the family differently. We discuss this in the context of the making of "responsible" decisions, and of the tensions that may arise within families between the best interests or wishes of a person and those of other family members. We hope this will clarify the reasoning of those who opt for non-engagement with medical genetic services and, more specifically, pre-symptomatic testing. Further, we hope it will be relevant for the provision of genetic counselling and psychosocial support to such families.
Identifiants
pubmed: 30573801
doi: 10.1038/s41431-018-0308-y
pii: 10.1038/s41431-018-0308-y
pmc: PMC6460576
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
353-359Références
Soc Sci Med. 2000 Sep;51(6):831-41
pubmed: 10972428
Community Genet. 1999;2(4):190-5
pubmed: 14960841
Soc Stud Sci. 2005 Feb;35(1):5-40
pubmed: 15991444
Clin Genet. 2006 Apr;69(4):297-305
pubmed: 16630162
Soc Sci Med. 2008 Apr;66(7):1521-32
pubmed: 18222583
Soc Sci Med. 2011 Jun;72(11):1810-6
pubmed: 20724050
J Genet Couns. 2012 Feb;21(1):101-12
pubmed: 21717286
J Health Psychol. 2002 Sep;7(5):491-508
pubmed: 22113136
Eur J Hum Genet. 2013 Mar;21(3):256-60
pubmed: 22892534
Genet Test Mol Biomarkers. 2012 Dec;16(12):1363-8
pubmed: 23153003
Clin Genet. 2013 Jun;83(6):518-24
pubmed: 23495852
JAMA Neurol. 2013 Jun;70(6):746-55
pubmed: 23609960
Sociol Health Illn. 2013 Nov;35(8):1227-41
pubmed: 23957884
Psychol Health. 2008;23(6):707-27
pubmed: 25160812
J Genet Couns. 2016 Feb;25(1):79-89
pubmed: 25986962
Eur J Hum Genet. 2016 Oct;24(10):1396-402
pubmed: 27165004
Bioethics. 2016 Oct;30(8):628-35
pubmed: 27523581
J Behav Med. 2017 Aug;40(4):583-594
pubmed: 28197815
Eur J Hum Genet. 2017 Jun;25(6):687-693
pubmed: 28327574
Soc Sci Med. 2017 Jun;182:73-80
pubmed: 28433926
Fam Process. 2018 Sep;57(3):836-846
pubmed: 28714147
Eur J Med Genet. 2018 Oct;61(10):575-580
pubmed: 29581083
Soc Sci Med. 1987;24(3):209-17
pubmed: 3469765
Adv Neurol. 1993;61:139-53
pubmed: 8421964
Eur J Hum Genet. 1997 Nov-Dec;5(6):351-63
pubmed: 9450179
Clin Genet. 1998 Dec;54(6):489-96
pubmed: 9894795