Literature DB >> 32700788

Whether, when, and how to communicate genetic risk to minors: 'I wanted more information but I think they were scared I couldn't handle it'.

Kelsey Stuttgen1,2, Allison McCague1,2, Juli Bollinger1, Rachel Dvoskin1, Debra Mathews1.   

Abstract

Genetic test results are often relevant not only to persons tested, but also to their children. Questions of whether, when, and how to disclose parental test results to children, particularly minors, can be difficult for parents to navigate. Currently, limited data are available on these questions from the perspective of minors. In this qualitative study, semi-structured interviews were conducted with parents affected by or at risk for hereditary cancer (N = 17) or Huntington's disease (N = 14) and their mature minor children aged 15-17 (N = 34). Parents and mature minors were interviewed separately. Genetic counselors (GCs; N = 19) were also interviewed. Most parents interviewed wanted to protect minors from genetic risk information (GRI) and feared minors would not be able to handle GRI. However, most mature minors reported they did not receive enough information and wished their parent was more forthcoming. Parents recommended taking time to process one's own test results before communicating with minors, and mature minors recommended parents communicate GRI in an honest, hopeful way. Most parents and GCs felt additional resources on communicating with minors about GRI and various genetic conditions are needed. This study includes the experiences and perspectives of a well-informed cohort, and results should be taken into careful consideration by parents, GCs, and others who are faced with communicating GRI to minors.
© 2020 National Society of Genetic Counselors.

Entities:  

Keywords:  Huntington's disease; adolescents; communication; ethics; family communication; hereditary cancer; parents; pediatrics

Mesh:

Year:  2020        PMID: 32700788      PMCID: PMC8564942          DOI: 10.1002/jgc4.1314

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  25 in total

1.  Living with genetic risk: effect on adolescent self-concept.

Authors:  Allyn McConkie-Rosell; Gail A Spiridigliozzi; Elizabeth Melvin; Deborah V Dawson; Ave M Lachiewicz
Journal:  Am J Med Genet C Semin Med Genet       Date:  2008-02-15       Impact factor: 3.908

Review 2.  Breast cancer statistics and prediction methodology: a systematic review and analysis.

Authors:  Ashutosh Kumar Dubey; Umesh Gupta; Sonal Jain
Journal:  Asian Pac J Cancer Prev       Date:  2015

3.  Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.

Authors:  D Ford; D F Easton; M Stratton; S Narod; D Goldgar; P Devilee; D T Bishop; B Weber; G Lenoir; J Chang-Claude; H Sobol; M D Teare; J Struewing; A Arason; S Scherneck; J Peto; T R Rebbeck; P Tonin; S Neuhausen; R Barkardottir; J Eyfjord; H Lynch; B A Ponder; S A Gayther; M Zelada-Hedman
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

4.  Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.

Authors:  Katja I Aktan-Collan; Helena A Kääriäinen; Eeva M Kolttola; Kirsi Pylvänäinen; Heikki J Järvinen; Ari H Haukkala; Jukka-Pekka Mecklin
Journal:  Fam Cancer       Date:  2011-03       Impact factor: 2.375

5.  Parents' communication with siblings of children affected by an inherited genetic condition.

Authors:  Gillian Plumridge; Alison Metcalfe; Jane Coad; Paramjit Gill
Journal:  J Genet Couns       Date:  2011-04-19       Impact factor: 2.537

6.  Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences.

Authors:  Alison Metcalfe; Gill Plumridge; Jane Coad; Andrew Shanks; Paramjit Gill
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246

7.  Breast cancer in young families: a qualitative interview study of fathers and their role and communication with their children following the diagnosis of maternal breast cancer.

Authors:  Gillian Forrest; Caroline Plumb; Sue Ziebland; Alan Stein
Journal:  Psychooncology       Date:  2009-01       Impact factor: 3.894

8.  How young people find out about their family history of Huntington's disease.

Authors:  Karen Forrest Keenan; Edwin van Teijlingen; Lorna McKee; Zosia Miedzybrodzka; Sheila A Simpson
Journal:  Soc Sci Med       Date:  2009-03-26       Impact factor: 4.634

9.  Models of consent to return of incidental findings in genomic research.

Authors:  Paul S Appelbaum; Erik Parens; Cameron R Waldman; Robert Klitzman; Abby Fyer; Josue Martinez; W Nicholson Price; Wendy K Chung
Journal:  Hastings Cent Rep       Date:  2014-06-11       Impact factor: 2.683

10.  Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening.

Authors:  Anita Gorrie; Alison D Archibald; Liane Ioannou; Lisette Curnow; Belinda McClaren
Journal:  J Community Genet       Date:  2017-10-02
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  1 in total

1.  Social support experiences when growing up with a parent with Huntington's disease.

Authors:  Siri Kjoelaas; Kristin B Feragen; Tine K Jensen
Journal:  Health Psychol Behav Med       Date:  2022-07-29
  1 in total

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