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The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer

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Summary

The present study investigated: (1) perception of genetic risk and, (2) the psychological effects of genetic counselling in women with a family history of breast cancer. Using a prospective design, with assessment pre- and post-genetic counselling at clinics and by postal follow-up at 1, 6 and 12 months, attenders at four South London genetic clinics were assessed. Participants included 282 women with a family history of breast cancer. Outcome was measured in terms of mental health, cancer-specific distress and risk perception. High levels of cancer-specific distress were found pre-genetic counselling, with 28% of participants reporting that they worried about breast cancer ‘frequently or constantly’ and 18% that worry about breast cancer was ‘a severe or definite problem’. Following genetic counselling, levels of cancer-specific distress were unchanged. General mental health remained unchanged over time (33% psychiatric cases detected pre-genetic counselling, 27% at 12 months after genetic counselling).

Prior to their genetics consultation, participants showed poor knowledge of their lifetime risk of breast cancer since there was no association between their perceived lifetime risk (when they were asked to express this as a 1 in x odds ratio) and their actual risk, when the latter was calculated by the geneticist at the clinic using the CASH model. In contrast, women were more accurate about their risk of breast cancer pre-genetic counselling when this was assessed in broad categorical terms (i.e. very much lower/very much higher than the average woman) with a significant association between this rating and the subsequently calculated CASH risk figure (P= 0.001). Genetic counselling produced a modest shift in the accuracy of perceived lifetime risk, expressed as an odds ratio, which was maintained at 12 months’ follow-up. A significant minority failed to benefit from genetic counselling; 77 women continued to over-estimate their risk and maintain high levels of cancer-related worry.

Most clinic attenders were inaccurate in their estimates of the population risk of breast cancer with only 24% able to give the correct figure prior to genetic counselling and 36% over-estimating this risk. There was some improvement following genetic counselling with 62% able to give the correct figure, but this information was poorly retained and this figure had dropped to 34% by the 1-year follow-up. The study showed that women attending for genetic counselling are worried about breast cancer, with 34% indicating that they had initiated the referral to the genetic clinic themselves. This anxiety is not alleviated by genetic counselling, although women reported that it was less of a problem at follow-up. Women who continue to over-estimate their risk and worry about breast cancer are likely to go on seeking unnecessary screening if they are not reassured.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

References

  • Claus, E. B., Risch, N. J. & Thompson, W. D. (1991). Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet 48: 232–242.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Evans, D. G. R., Blair, V., Greenhalgh, R., Hopwood, P. & Howell, A. (1994). The impact of genetic counselling on risk perception in women with a family history of breast cancer. Br J Cancer 70: 934–938.

    CAS  Article  Google Scholar 

  • Goldberg, D. & Williams, P. (1988). A User’s Guide to the General Health Questionnaire, NFER-Nelson: Windsor, UK

    Google Scholar 

  • Green, C. H. & Brown, R. A. (1978). Counting lives. J Occ Accidents 2: 55

    Article  Google Scholar 

  • Horowitz, M., Wilner, N. & Alvarez, W. (1979). Impact of events scale: a measure of subjective stress. Psychosom Med 41: 209–218.

    CAS  Article  Google Scholar 

  • Kash, K. M., Holland, J. C., Halper, M. S. & Miller, D. G. (1992). Psychological distress and surveillance behaviours of women with a family history of breast cancer. J Natl Cancer Inst 84: 24–30.

    CAS  Article  Google Scholar 

  • Leonard, C., Chase, G. & Child, B. (1972). Genetic counselling, a consumer’s view. N Engl J Med 287: 433

    CAS  Article  Google Scholar 

  • Lerman, C. & Schwartz, M. (1993). Adherence and psychological adjustment among women at high risk for breast cancer. Breast Cancer Res Treat 28: 145–155.

    CAS  Article  Google Scholar 

  • Lerman, C., Trock, B., Rimer, B., Boyce, A., Jepson, C. & Engstrom, P. (1991). Psychological and behavioral implications of abnormal mammograms. Ann Int Med 114: 657–661.

    CAS  Article  Google Scholar 

  • Lloyd, S., Watson, M., Waites, B., Meyer, L., Eeles, R., Ebbs, S. & Tylee, A. (1996). Familial breast cancer: a controlled study of risk perception, psychological morbidity and health beliefs in women attending for genetic counselling. Br J Cancer 74: 482–487.

    CAS  Article  Google Scholar 

  • May, S. (1992). Patient satisfaction and the detection of psychiatric morbidity in general practice. Family Practice 9: 76–81.

    CAS  Article  Google Scholar 

  • Morris, T. & Greer, S. (1982). Psychological characteristics of women electing to attend a breast screening clinic. Clin Oncol 8: 113–119.

    CAS  PubMed  Google Scholar 

  • Miki, Y., Swensen, J., Shattuck-Eidens, D., Futreal, A., Harshman, K., Tavtigian, S. & Lui, Q. (1994). A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266: 66–71.

    CAS  Article  Google Scholar 

  • Spielberger, C. D. (1983). State-Trait Anxiety Inventory for Adults, Consulting Psychologists’ Press: Palo Alto, CA

    Google Scholar 

  • Watson, M., Lloyd, S., Eeles, R., Ponder, B., Easton, D., Seal, S., Averill, D., Daly, P., Ormiston, W. & Murday, V. (1996). Psychosocial impact of testing (by linkage) for the BRCA1 breast cancer gene: an investigation of two families in the research setting. Psycho-oncology 5: 233–239.

    Article  Google Scholar 

  • Watson, M., Duvivier, V., Wade Walsh, M., Ashley, S., Papaikonomou, M., Eeles, R., Sacks, N. & Murday, V. (1998). Family history of breast cancer: what do women understand and recall about their genetic risk? J Med Genetics 35: 731–738.

    CAS  Article  Google Scholar 

  • Wooster, R., Bignell, G., Lancaster, J., Swift, S., Seal, S. & Mangion, J. (1995). Identification of the breast cancer susceptibility gene BRCA2. Nature 378: 789–792.

    CAS  Article  Google Scholar 

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Watson, M., Lloyd, S., Davidson, J. et al. The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer. Br J Cancer 79, 868–874 (1999). https://doi.org/10.1038/sj.bjc.6690139

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