Literature DB >> 11180589

The psychological consequences of offering mutation searching in the family for those at risk of hereditary breast and ovarian cancer--a pilot study.

M Broadstock1, S Michie, J Gray, J Mackay, T M Marteau.   

Abstract

AIM: To describe the short and longer-term psychological consequences of waiting for the results of mutation searching (MS) amongst those at risk of hereditary breast and ovarian cancer (HBOC).
DESIGN: A prospective study, with measures before the offer of a mutation search, and 1 week, 6 months and 12 months afterwards. SAMPLE: 21 unaffected women at risk of HBOC offered MS in an affected relative at one of two UK regional genetics centres. OUTCOME MEASURES: Standardized questionnaire measures of general anxiety, general distress, distress about cancer in the family and cancer-specific worries.
RESULTS: Mutation searches were initiated in 15 of 21 families; two received results within 12 months. For the 13 still waiting for results, levels of anxiety and distress were within normal ranges at all time-points. They reported reduced worries about cancer 6 and 12 months post-search offer compared with earlier assessments, but experienced an increase in general anxiety 12 months since the search offer. These changes over time were not found in those not waiting for the results of a mutation search.
CONCLUSION: The majority of women were without a result 12 months after being offered MS. Whilst these women were less worried about cancer in the 6 months after initiating the testing process, their anxiety levels increased 12 months since the offer of a mutation search. Seeing a specialist seems to reduce cancer worries. There may, however, be long-term psychological costs of offering tests that are unlikely to give results in a foreseeable future.

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Mesh:

Year:  2000        PMID: 11180589     DOI: 10.1002/1099-1611(200011/12)9:6<537::aid-pon479>3.0.co;2-u

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  11 in total

Review 1.  Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review.

Authors:  R Timman; T Stijnen; A Tibben
Journal:  J Med Genet       Date:  2004-07       Impact factor: 6.318

2.  Short- and long-term impact of receiving genetic mutation results in women at increased risk for hereditary breast cancer.

Authors:  Jacqueline Lim; Mariette Macluran; Melanie Price; Barbara Bennett; Phyllis Butow
Journal:  J Genet Couns       Date:  2004-04       Impact factor: 2.537

Review 3.  How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: systematic review.

Authors:  Stephanie Sivell; Glyn Elwyn; Clara L Gaff; Angus J Clarke; Rachel Iredale; Chris Shaw; Joanna Dundon; Hazel Thornton; Adrian Edwards
Journal:  J Genet Couns       Date:  2007-10-30       Impact factor: 2.537

4.  Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations.

Authors:  Amy Østertun Geirdal; Jon G Reichelt; Alv A Dahl; Ketil Heimdal; Lovise Maehle; Astrid Stormorken; Pål Møller
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

Review 5.  Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers.

Authors:  Susan T Vadaparampil; Mary Ropka; Michael E Stefanek
Journal:  Fam Cancer       Date:  2005       Impact factor: 2.375

6.  Predictive genetic testing for hereditary breast and ovarian cancer: psychological distress and illness representations 1 year following disclosure.

Authors:  E Claes; G Evers-Kiebooms; L Denayer; M Decruyenaere; A Boogaerts; K Philippe; E Legius
Journal:  J Genet Couns       Date:  2005-10       Impact factor: 2.537

7.  Quality of life and its relation to cancer-related stress in women of families with hereditary cancer without demonstrated mutation.

Authors:  Amy Østertun Geirdal; Lovise Maehle; Ketil Heimdal; Astrid Stormorken; Pål Møller; Alv A Dahl
Journal:  Qual Life Res       Date:  2006-04       Impact factor: 4.147

8.  The information and support needs of women at high risk of familial breast and ovarian cancer: how can cancer genetic services give patients what they want?

Authors:  Rachel Iredale; Kate Brain; Jonathon Gray; Elizabeth France
Journal:  Fam Cancer       Date:  2003       Impact factor: 2.375

9.  Development and pilot testing of two decision aids for individuals considering genetic testing for cancer risk.

Authors:  Claire E Wakefield; Bettina Meiser; Judi Homewood; Michelle Peate; Judy Kirk; Beverley Warner; Elizabeth Lobb; Clara Gaff; Kathy Tucker
Journal:  J Genet Couns       Date:  2007-02-23       Impact factor: 2.717

10.  Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study.

Authors:  Mary Jane Esplen; Mario Cappelli; Jiahui Wong; Joan L Bottorff; Jon Hunter; June Carroll; Michel Dorval; Brenda Wilson; Judith Allanson; Kara Semotiuk; Melyssa Aronson; Louise Bordeleau; Nicole Charlemagne; Wendy Meschino
Journal:  BMJ Open       Date:  2013-03-13       Impact factor: 2.692

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