Literature DB >> 29476166

Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes.

Erin Turbitt1, Megan C Roberts2, Rebecca A Ferrer2, Jennifer M Taber3, Katie L Lewis4, Leslie G Biesecker4, Barbara B Biesecker5, William Mp Klein5,2.   

Abstract

Given familial implications of genetic information, it is important to understand intentions to share carrier results with family members. To our knowledge, no studies among individuals undergoing exome sequencing have used dyadic data analysis to examine the effect of spousal perceptions and beliefs. Survey responses from 136 individuals (68 couples) undergoing exome sequencing in a research study were analyzed using dyadic analysis (the actor-partner interdependence model). Intention to share carrier results with family members was correlated between spouses (ICC = 0.43; 95% CI: 0.21-0.61; p = 0.004), as was worry about risk of a genetic condition in the family (ICC = 0.45; 95% CI: 0.24-0.62; p < 0.001). Perceived value of result and worry about risk of a genetic condition in the family were associated with one's own intentions to share carrier results. However, spousal status on these variables did not explain additional variance in an individual's intentions. Although we found no partner effects on intentions, spouses have comparable intentions to share carrier results, suggesting it may be important to account for non-independence in other research studies.

Mesh:

Year:  2018        PMID: 29476166      PMCID: PMC5945607          DOI: 10.1038/s41431-018-0118-2

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  18 in total

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Authors:  Valentim R Alferes; David A Kenny
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Review 4.  Diagnostic clinical genome and exome sequencing.

Authors:  Leslie G Biesecker; Robert C Green
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Authors:  Joan K Monin; Becca Levy; Baibing Chen; Terri Fried; Sarah T Stahl; Richard Schulz; Margaret Doyle; Trace Kershaw
Journal:  Ann Behav Med       Date:  2015-10

6.  Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.

Authors:  Flavia M Facio; Haley Eidem; Tyler Fisher; Stephanie Brooks; Amy Linn; Kimberly A Kaphingst; Leslie G Biesecker; Barbara B Biesecker
Journal:  Eur J Hum Genet       Date:  2012-08-15       Impact factor: 4.246

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8.  A family genetic risk communication framework: guiding tool development in genetics health services.

Authors:  Miriam E Wiens; Brenda J Wilson; Christina Honeywell; Holly Etchegary
Journal:  J Community Genet       Date:  2013-01-15

9.  The influence of partner's behavior on health behavior change: the English Longitudinal Study of Ageing.

Authors:  Sarah E Jackson; Andrew Steptoe; Jane Wardle
Journal:  JAMA Intern Med       Date:  2015-03       Impact factor: 21.873

10.  Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.

Authors:  Katie L Lewis; Paul K J Han; Gillian W Hooker; William M P Klein; Leslie G Biesecker; Barbara B Biesecker
Journal:  PLoS One       Date:  2015-07-17       Impact factor: 3.240

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  1 in total

1.  Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing.

Authors:  Chloe O Huelsnitz; Erin Turbitt; Jennifer M Taber; Katie L Lewis; Leslie G Biesecker; Barbara B Biesecker; William M P Klein
Journal:  J Behav Med       Date:  2021-05-13
  1 in total

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