Literature DB >> 31505002

Perceptions of uncertainties about carrier results identified by exome sequencing in a randomized controlled trial.

Kendall L Umstead1, Paul K J Han2, Katie L Lewis3, Ilana M Miller3, Charlotte L Hepler1, Lydia J Thompson1, Tyra G Wolfsberg4, Anh-Dao Nguyen4, Mark T Fredriksen4, Gretchen Gibney4, Erin Turbitt1, Leslie G Biesecker3, Barbara B Biesecker1.   

Abstract

How individuals perceive uncertainties in sequencing results may affect their clinical utility. The purpose of this study was to explore perceptions of uncertainties in carrier results and how they relate to psychological well-being and health behavior. Post-reproductive adults (N = 462) were randomized to receive carrier results from sequencing through either a web platform or a genetic counselor. On average, participants received two results. Group differences in affective, evaluative, and clinical uncertainties were assessed from baseline to 1 and 6 months; associations with test-specific distress and communication of results were assessed at 6 months. Reductions in affective uncertainty (∆x̅ = 0.78, 95% CI: 0.53, 1.02) and evaluative uncertainty (∆x̅ = 0.69, 95% CI: 0.51, 0.87) followed receipt of results regardless of randomization arm at 1 month. Participants in the web platform arm reported greater clinical uncertainty than those in the genetic counselor arm at 1 and 6 months; this was corroborated by the 1,230 questions asked of the genetic counselor and residual questions reported by those randomized to the web platform. Evaluative uncertainty was associated with a lower likelihood of communicating results to health care providers. Clinical uncertainty was associated with a lower likelihood of communicating results to children. Learning one's carrier results may reduce perceptions of uncertainties, though web-based return may lead to less reduction in clinical uncertainty in the short term. These findings warrant reinforcement of clinical implications to minimize residual questions and promote appropriate health behavior (communicating results to at-risk relatives in the case of carrier results), especially when testing alternative delivery models. © Society of Behavioral Medicine 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Carrier testing; Genetic counseling; Genome sequencing; Uncertainty; Web platform

Mesh:

Year:  2020        PMID: 31505002      PMCID: PMC7237536          DOI: 10.1093/tbm/ibz111

Source DB:  PubMed          Journal:  Transl Behav Med        ISSN: 1613-9860            Impact factor:   3.046


  16 in total

1.  Perceived ambiguity as a barrier to intentions to learn genome sequencing results.

Authors:  Jennifer M Taber; William M P Klein; Rebecca A Ferrer; Paul K J Han; Katie L Lewis; Leslie G Biesecker; Barbara B Biesecker
Journal:  J Behav Med       Date:  2015-05-24

2.  Ability of Patients to Distinguish Among Cardiac Genomic Variant Subclassifications.

Authors:  Lydia D Hellwig; Barbara B Biesecker; Katie L Lewis; Leslie G Biesecker; Cynthia A James; William M P Klein
Journal:  Circ Genom Precis Med       Date:  2018-06

3.  PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.

Authors:  B B Biesecker; S W Woolford; W M P Klein; K B Brothers; K L Umstead; K L Lewis; L G Biesecker; P K J Han
Journal:  Clin Genet       Date:  2017-01-30       Impact factor: 4.438

Review 4.  Diagnostic clinical genome and exome sequencing.

Authors:  Leslie G Biesecker; Robert C Green
Journal:  N Engl J Med       Date:  2014-06-19       Impact factor: 91.245

5.  Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial.

Authors:  Katie L Lewis; Kendall L Umstead; Jennifer J Johnston; Ilana M Miller; Lydia J Thompson; Kristen P Fishler; Leslie G Biesecker; Barbara B Biesecker
Journal:  Am J Hum Genet       Date:  2018-03-08       Impact factor: 11.025

6.  A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.

Authors:  David Cella; Chanita Hughes; Amy Peterman; Chih-Hung Chang; Beth N Peshkin; Marc D Schwartz; Lari Wenzel; Amy Lemke; Alfred C Marcus; Caryn Lerman
Journal:  Health Psychol       Date:  2002-11       Impact factor: 4.267

7.  Carrier testing for severe childhood recessive diseases by next-generation sequencing.

Authors:  Callum J Bell; Darrell L Dinwiddie; Neil A Miller; Shannon L Hateley; Elena E Ganusova; Joann Mudge; Ray J Langley; Lu Zhang; Clarence C Lee; Faye D Schilkey; Vrunda Sheth; Jimmy E Woodward; Heather E Peckham; Gary P Schroth; Ryan W Kim; Stephen F Kingsmore
Journal:  Sci Transl Med       Date:  2011-01-12       Impact factor: 17.956

8.  Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.

Authors:  Barbara B Biesecker; Katie L Lewis; Kendall L Umstead; Jennifer J Johnston; Erin Turbitt; Kristen P Fishler; John H Patton; Ilana M Miller; Alexis R Heidlebaugh; Leslie G Biesecker
Journal:  JAMA Intern Med       Date:  2018-03-01       Impact factor: 21.873

9.  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

10.  Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.

Authors:  Saskia C Sanderson; Michael D Linderman; Sabrina A Suckiel; Randi Zinberg; Melissa Wasserstein; Andrew Kasarskis; George A Diaz; Eric E Schadt
Journal:  Eur J Hum Genet       Date:  2017-01-04       Impact factor: 4.246

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  1 in total

1.  Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.

Authors:  Tamara S Roman; Stephanie B Crowley; Myra I Roche; Ann Katherine M Foreman; Julianne M O'Daniel; Bryce A Seifert; Kristy Lee; Alicia Brandt; Chelsea Gustafson; Daniela M DeCristo; Natasha T Strande; Lori Ramkissoon; Laura V Milko; Phillips Owen; Sayanty Roy; Mai Xiong; Ryan S Paquin; Rita M Butterfield; Megan A Lewis; Katherine J Souris; Donald B Bailey; Christine Rini; Jessica K Booker; Bradford C Powell; Karen E Weck; Cynthia M Powell; Jonathan S Berg
Journal:  Am J Hum Genet       Date:  2020-08-26       Impact factor: 11.025

  1 in total

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