Literature DB >> 22429077

Toward a new understanding of risk perception among young female BRCA1/2 "previvors".

Lindsey M Hoskins1, Kevin M Roy, Mark H Greene.   

Abstract

The quantitative risk of cancer among BRCA1/2 gene mutation carriers is generally well-understood, and can be communicated clearly to potential and known mutation carriers during the genetic risk assessment, education, and testing process. The extent to which individual mutation carriers feel vulnerable to cancer is a more complex dynamic with a powerful effect on risk-management decision-making; however, these decisions are not the products of straightforward personal assessment of one's quantitative probability of being diagnosed with cancer. We undertook this National Cancer Institute study to broaden understanding of the lived experiences of women who learn early in the life course that they carry a BRCA1/2 mutation. Our data indicate that the relationship between perceived risk and risk-management decisions is not direct, that is, several nononcologic components of risk are also integral to women's management decision-making. High-risk women commonly utilize self-perceived cancer risk to shape their decision-making and communication about various tasks of young adulthood, including differentiation from family of origin, establishing a permanent couple relationship, and family formation. Risk-management is also an important domain in which they strive to take control of their lives by actively participating in management choices. By understanding how these complex dynamics fit together, care providers can better guide, counsel, and support high-risk women as they struggle to balance legitimate risk-reduction needs with the desire to live a normal life. Here we present data from our qualitative research to aid in this effort.

Entities:  

Mesh:

Year:  2012        PMID: 22429077     DOI: 10.1037/a0027276

Source DB:  PubMed          Journal:  Fam Syst Health        ISSN: 1091-7527            Impact factor:   1.950


  16 in total

1.  Illness perceptions, risk perception and worry in SDH mutation carriers.

Authors:  L T van Hulsteijn; A A Kaptein; A Louisse; N R Biermasz; J W A Smit; E P M Corssmit
Journal:  Fam Cancer       Date:  2014-03       Impact factor: 2.375

2.  Heightened perception of breast cancer risk in young women at risk of familial breast cancer.

Authors:  Rachael Glassey; Moira O'Connor; Angela Ives; Christobel Saunders; Sarah O'Sullivan; Sarah J Hardcastle
Journal:  Fam Cancer       Date:  2018-01       Impact factor: 2.375

Review 3.  Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.

Authors:  Alison L Young; Phyllis N Butow; Janine Vetsch; Veronica F Quinn; Andrea F Patenaude; Katherine M Tucker; Claire E Wakefield
Journal:  J Genet Couns       Date:  2017-06-30       Impact factor: 2.537

4.  Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.

Authors:  Rachel Shapira; Erin Turbitt; Lori H Erby; Barbara B Biesecker; William M P Klein; Gillian W Hooker
Journal:  Fam Cancer       Date:  2018-10       Impact factor: 2.375

5.  Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population.

Authors:  Suzanne C O'Neill; Chalanda Evans; Rebekah J Hamilton; Beth N Peshkin; Claudine Isaacs; Sue Friedman; Kenneth P Tercyak
Journal:  Fam Cancer       Date:  2018-07       Impact factor: 2.375

6.  "My funky genetics": BRCA1/2 mutation carriers' understanding of genetic inheritance and reproductive merger in the context of new reprogenetic technologies.

Authors:  Allison Werner-Lin; Lisa R Rubin; Maya Doyle; Rikki Stern; Katie Savin; Karen Hurley; Michal Sagi
Journal:  Fam Syst Health       Date:  2012-06       Impact factor: 1.950

7.  Comparison of the screening practices of unaffected noncarriers under 40 and between 40 and 49 in BRCA1/2 families.

Authors:  Christelle Duprez; Véronique Christophe; Isabelle Milhabet; Aurélie Krzeminski; Claude Adenis; Pascaline Berthet; Jean-Philippe Peyrat; Philippe Vennin
Journal:  J Genet Couns       Date:  2013-01-25       Impact factor: 2.537

8.  Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer.

Authors:  Rhona MacLeod; Anna Beach; Sasha Henriques; Jasmin Knopp; Katie Nelson; Lauren Kerzin-Storrar
Journal:  Eur J Hum Genet       Date:  2013-07-17       Impact factor: 4.246

9.  A survey of genetic counselors about the needs of 18-25 year olds from families with hereditary breast and ovarian cancer syndrome.

Authors:  Allison Werner-Lin; Rachel Ratner; Lindsey M Hoskins; Caroline Lieber
Journal:  J Genet Couns       Date:  2014-07-12       Impact factor: 2.537

10.  Breast cancer in the young: role of the geneticist.

Authors:  Ashley H Woodson; Jessica L Profato; Kimberly I Muse; Jennifer K Litton
Journal:  J Thorac Dis       Date:  2013-06       Impact factor: 2.895

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