Journal article
Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age
Journal of genetic counseling, Vol.26(1), pp.173-181
02/2017
DOI: 10.1007/s10897-016-9995-0
PMCID: PMC5239754
PMID: 27422778
Abstract
Genetic test results have medical implications beyond the patient that extend to biological family members. We examined psychosocial and clinical factors associated with communication of genetic test results within families. Women (N = 1080) diagnosed with breast cancer at age 40 or younger completed an online survey; 920 women that reported prior cancer genetic testing were included in analysis. We examined the proportion of immediate family members to whom they communicated genetic test results, and built multivariable regression models to examine clinical and psychosocial variables associated with the proportion score. Participants were most likely to communicate test results to their mother (83 %) and least likely to their son (45 %). Participants who carried a BRCA mutation (OR = 1.34; 95 % CI = 1.06, 1.70), had higher interest in genomic information (OR = 1.55; 95 % CI = 1.26, 1.91) and lower genetic worry (OR = 0.91; 95 % CI = 0.86, 0.96) communicated genetic test results to a greater proportion of their immediate family members. Participants with a BRCA1/2 mutation shared their genetic test results with more male family members (OR = 1.72; 95 % CI = 1.02, 2.89). Our findings suggest that patients with high worry about genetic risks, low interest in genomic information, or receive a negative genetic test result will likely need additional support to encourage family communication.
Details
- Title: Subtitle
- Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age
- Creators
- Ashley Elrick - Department of Communication, University of Utah, 255 Central Campus Drive, LNCO, Salt Lake City, UT, 84112, USA. Ashley.Elrick@hci.utah.eduSato Ashida - College of Public Health, University of Iowa, Iowa City, IA, USAJennifer Ivanovich - Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USASarah Lyons - Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USABarbara B Biesecker - Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD, USAMelody S Goodman - Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USAKimberly A Kaphingst - Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA
- Resource Type
- Journal article
- Publication Details
- Journal of genetic counseling, Vol.26(1), pp.173-181
- DOI
- 10.1007/s10897-016-9995-0
- PMID
- 27422778
- PMCID
- PMC5239754
- NLM abbreviation
- J Genet Couns
- ISSN
- 1059-7700
- eISSN
- 1573-3599
- Publisher
- United States
- Grant note
- R01 CA168608 / NCI NIH HHS
- Language
- English
- Date published
- 02/2017
- Academic Unit
- Injury Prevention Research Center; Public Policy Center (Archive); Community and Behavioral Health
- Record Identifier
- 9984063140402771
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