Literature DB >> 18230020

Interpersonal responses among sibling dyads tested for BRCA1/BRCA2 gene mutations.

Heidi A Hamann1, Timothy W Smith, Ken R Smith, Robert T Croyle, John M Ruiz, John C Kircher, Jeffrey R Botkin.   

Abstract

OBJECTIVE: The familial context plays an important role in psychosocial responses to genetic testing. The purpose of this study was to compare sibling pairs with different combinations of BRCA1/BRCA2 test results on measures of affect, interpersonal responses, and physiological reactions.
DESIGN: Forty-nine sibling dyads with different combinations of BRCA1/BRCA2 test results (i.e., mixed, positive, negative) completed a questionnaire, and 35 of the dyads also participated in a laboratory-based discussion of genetic testing. MAIN OUTCOME MEASURES: The primary outcome variables included participant reports of supportive actions toward their sibling, state anger and anxiety, perceptions of sibling behavior, and electrodermal responses.
RESULTS: Compared to positive and negative dyads, mixed pairs reported less friendly general support actions, noted more anger, and perceived their sibling to be less friendly and more dominant during the interactions. In comparisons between same-result (i.e., positive, negative) pairs, positive dyads reported more dominant support behaviors and perceived their sibling to be friendlier during the interactions.
CONCLUSION: Data suggest that siblings who have different test results may experience more interpersonal strain than siblings who have the same test result. Future research on genetic testing and family relationships can expand upon these findings.

Entities:  

Mesh:

Year:  2008        PMID: 18230020      PMCID: PMC3704327          DOI: 10.1037/0278-6133.27.1.100

Source DB:  PubMed          Journal:  Health Psychol        ISSN: 0278-6133            Impact factor:   4.267


  24 in total

1.  A power primer.

Authors:  J Cohen
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2.  A model protocol for evaluating the behavioral and psychosocial effects of BRCA1 testing.

Authors:  J R Botkin; R T Croyle; K R Smith; B J Baty; C Lerman; D E Goldgar; J M Ward; B J Flick; J E Nash
Journal:  J Natl Cancer Inst       Date:  1996-07-03       Impact factor: 13.506

3.  BRCA1 Testing: Genetic Counseling Protocol Development and Counseling Issues.

Authors:  B J Baty; V L Venne; J McDonald; R T Croyle; C Halls; J E Nash; J R Botkin
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4.  Reinventing the wheel.

Authors:  S Kessler
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5.  Effects of spouses on distress experienced by BRCA1 mutation carriers over time.

Authors:  Jean E Wylie; Ken R Smith; Jeffrey R Botkin
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-05-15       Impact factor: 3.908

6.  Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.

Authors:  S A Gayther; J Mangion; P Russell; S Seal; R Barfoot; B A Ponder; M R Stratton; D Easton
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

7.  BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships.

Authors:  Aideen McInerney-Leo; Barbara Bowles Biesecker; Donald W Hadley; Ronald G Kase; Therese R Giambarresi; Elizabeth Johnson; Caryn Lerman; Jeffery P Struewing
Journal:  Am J Med Genet A       Date:  2005-03-01       Impact factor: 2.802

8.  Cancer Incidence in BRCA1 mutation carriers.

Authors:  Deborah Thompson; Douglas F Easton
Journal:  J Natl Cancer Inst       Date:  2002-09-18       Impact factor: 13.506

9.  Predictive testing for Huntington disease in Canada: adverse effects and unexpected results in those receiving a decreased risk.

Authors:  M Huggins; M Bloch; S Wiggins; S Adam; O Suchowersky; M Trew; M Klimek; C R Greenberg; M Eleff; L P Thompson
Journal:  Am J Med Genet       Date:  1992-02-15

10.  Attitudes of persons at risk for Huntington disease toward predictive testing.

Authors:  S Kessler; T Field; L Worth; H Mosbarger
Journal:  Am J Med Genet       Date:  1987-02
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  6 in total

1.  Stigmatization and male identity: Norwegian males' experience after identification as BRCA1/2 mutation carriers.

Authors:  Nina Strømsvik; Målfrid Råheim; Nina Oyen; Lars Fredrik Engebretsen; Eva Gjengedal
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2.  Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations.

Authors:  Claustre Pont-Sunyer; Susan Bressman; Deborah Raymond; Amanda Glickman; Eduardo Tolosa; Rachel Saunders-Pullman
Journal:  Mov Disord       Date:  2015-05-07       Impact factor: 10.338

3.  Genomic Essentialism: Its Provenance and Trajectory as an Anticipatory Ethical Concern.

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Journal:  Hastings Cent Rep       Date:  2019-05       Impact factor: 2.683

4.  Exploring psychological responses to genetic testing for Lynch Syndrome within the family context.

Authors:  Dina Eliezer; Donald W Hadley; Laura M Koehly
Journal:  Psychooncology       Date:  2014-05-28       Impact factor: 3.894

Review 5.  Family Adjustment to Hereditary Cancer Syndromes: A Systematic Review.

Authors:  Pedro Gomes; Giada Pietrabissa; Eunice R Silva; João Silva; Paula Mena Matos; Maria Emília Costa; Vanessa Bertuzzi; Eliana Silva; Maria Carolina Neves; Célia M D Sales
Journal:  Int J Environ Res Public Health       Date:  2022-01-30       Impact factor: 3.390

6.  Generation after generation: exploring the psychological impact of providing genetic services through a cascading approach.

Authors:  Donald W Hadley; Sato Ashida; Jean F Jenkins; Jean C Martin; Kathleen A Calzone; Natalia R Kuhn; Colleen M McBride; Ilan R Kirsch; Laura M Koehly
Journal:  Genet Med       Date:  2010-12       Impact factor: 8.822

  6 in total

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