Family Communication Patterns and Challenges of Huntington's Disease Risk, the Decision to Pursue Presymptomatic Testing, and Test Results
- PMID: 32568103
- PMCID: PMC7569676
- DOI: 10.3233/JHD-200402
Family Communication Patterns and Challenges of Huntington's Disease Risk, the Decision to Pursue Presymptomatic Testing, and Test Results
Abstract
Background: Communicating genetic information within families can provide individuals with the emotional support, alert family members to their own potential risk, and strengthen relationships. However, these communications have the potential to cause emotional distress to individuals and family members if family members are informed of a risk they do not wish to know or discuss. Communication about the decision to pursue testing and test results are especially sensitive in Huntington's disease (HD), where individuals often feel strongly about either knowing or not knowing their genetic status.
Objective: To examine family communication patterns of genetic risk, the decision to pursue testing, and test results not just years, but decades after testing for HD, and examine how family communication of genetic risk information affects family relationships over the long-term.
Methods: In this qualitative study, 39 semi-structured interviews were conducted with probands who went through genetic testing for HD. Clinic notes from these individuals were also analyzed.
Results: Family communication patterns varied based on relation (e.g., significant others, child, extended family) and were influenced by a variety of factors. Sharing with spouses and children had a positive influence on the relationship in most cases. Sharing with extended family members had varying effects on relationships. Negative effects were more likely when family members were in denial, had not pursued testing for themselves, or did not support testing.
Conclusion: Communication to significant others and children, should be discussed with and supported in individuals seeking testing for HD, but for extended family members, potential effects on the relationship, emotional distress, and benefits should be discussed and weighed.
Keywords: Communication; Huntington’s disease; family relations; genetic testing.
Conflict of interest statement
Conflict of Interest
All of the authors declare that they have no conflicts of interest.
Similar articles
-
Psychosocial impact on individuals who received negative test results from predictive testing for Huntington's disease: An exploratory qualitative study.J Genet Couns. 2025 Apr;34(2):e1981. doi: 10.1002/jgc4.1981. Epub 2024 Oct 4. J Genet Couns. 2025. PMID: 39367595
-
Perspectives towards predictive testing in Huntington disease.Neurol India. 2006 Dec;54(4):359-62. doi: 10.4103/0028-3886.28105. Neurol India. 2006. PMID: 17114842
-
Analysis of the Reasons for Non-Uptake of Predictive Testing for Huntington's Disease in Spain: A Qualitative Study.J Genet Couns. 2015 Dec;24(6):1011-21. doi: 10.1007/s10897-015-9840-x. Epub 2015 Apr 30. J Genet Couns. 2015. PMID: 25921556
-
Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas.Prenat Diagn. 1998 Dec;18(13):1422-6. doi: 10.1002/(sici)1097-0223(199812)18:13<1422::aid-pd499>3.0.co;2-r. Prenat Diagn. 1998. PMID: 9949442 Review.
-
Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.Rev Neurol (Paris). 2015 Jun-Jul;171(6-7):572-80. doi: 10.1016/j.neurol.2015.02.016. Epub 2015 May 19. Rev Neurol (Paris). 2015. PMID: 26002494 Review.
Cited by
-
Factors that Influence Intent to Share Genetic Information Related to Cancer Risk with Family Members.J Health Commun. 2021 Aug 3;26(8):545-552. doi: 10.1080/10810730.2021.1968078. Epub 2021 Sep 2. J Health Commun. 2021. PMID: 34473010 Free PMC article.
-
Predictive genetic testing for Huntington's disease: Exploring participant experiences of uncertainty and ambivalence between clinic appointments.J Genet Couns. 2025 Feb;34(1):e1911. doi: 10.1002/jgc4.1911. Epub 2024 May 13. J Genet Couns. 2025. PMID: 38741209 Free PMC article.
References
-
- Ross CA, Aylward EH, Wild EJ, Langbehn DR, Long JD, Warner JH, et al. Huntington disease: natural history, biomarkers and prospects for therapeutics. Nat Rev Neurol. 2014. April;10(4):204–16. - PubMed
-
- Sobel SK, Cowan DB. Impact of genetic testing for Huntington disease on the family system. Am J Med Genet. 2000. January 3;90(1):49–59. - PubMed
-
- Brandt J, Quaid KA, Folstein SE. Presymptomatic DNA testing for Huntington’s disease. The J of Neuropsychiatry Clin Neurosci. 1989;1(2):195–197 - PubMed
-
- Forrest K, Simpson SA, Wilson BJ, Van Teijlingen ER, McKee L, Haites N, et al. To tell or not to tell: barriers and facilitators in family communication about genetic risk. Clin Genet. 2003. October;64(4):317–26. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical