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Journal ArticleDOI

Genetic testing for breast cancer susceptibility: Awareness and interest among women in the general population

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TLDR
The extent to which a group of female HMO enrollees were aware of the discovery of the BRCA1 gene and whether they would be interested in being tested to find out if they have the gene was examined to have implications for education and counseling.
Abstract
Previous research has suggested that demand for genetic testing for breast cancer susceptibility may be quite high, even among those at relatively low risk of carrying a mutation. This study examined the extent to which a group of female HMO enrollees were aware of the discovery of the BRCA1 gene and, without having received detailed information about the test, whether they would be interested in being tested to find out if they have the gene. Factors associated with awareness of and interest in testing were also examined. Four hundred seventy-three women age 50 and over, almost all of whom did not have an increased risk of breast cancer based on family history, were surveyed by telephone. Fifty-one percent of respondents had heard about the discovery of a breast cancer gene. In logistic regression analysis, women who described themselves as comfortable financially, had at least some college education, and were premenopausal were more likely to have heard of the gene discovery than women who were not comfortable financially, had no more than a high school education, and were postmenopausal. Sixty-nine percent of the respondents said that they would be interested in being tested to find out if they had a breast cancer gene. Women who were younger than 60, white, believed their family would benefit if they had a mammogram, and believed that regular mammograms give them a feeling of control over their health, were more likely to be interested in testing than those who were 60 or older, African-American or other, and did not believe that their family would benefit if they had a mammogram or that mammograms give them a feeling of control over their health. These findings have implications for education and counseling. Women who express an interest in being tested must be made fully aware of the limitations and possible consequences of testing. Special efforts may be needed to make information about testing available to women who have low levels of education.

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Citations
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Logistic regression in the medical literature: standards for use and reporting, with particular attention to one medical domain.

TL;DR: Substantial shortcomings were found in both use of LR and reporting of results, and it is recommended that authors, reviewers, and editors pay greater attention to guidelines concerning the use and Reporting of LR models.
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Racial Differences in the Use of BRCA1/2 Testing Among Women With a Family History of Breast or Ovarian Cancer

TL;DR: Investigation of the relationship between race and the use of BRCA1/2 counseling among women with a family history of breast or ovarian cancer found racial disparities are large and do not appear to be explained by differences in risk factors for carrying a BRCa1/ 2 mutation, socioeconomic factors, risk perception, attitudes, or primary care physician recommendations.
Journal ArticleDOI

Genetic testing: psychological aspects and implications.

TL;DR: A review of the literature concerning prenatal, carrier, and predictive genetic testing suggests that the severity of psychological risks posed by research-based genetic testing is not great, however, subgroups of individuals with particular psychological traits may be more vulnerable to adverse effects.
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Attitudes toward colon cancer gene testing: factors predicting test uptake.

TL;DR: The findings of this study are consistent with the associations reported between psychological factors and other cancer screening behaviors.
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US physicians' attitudes toward genetic testing for cancer susceptibility.

TL;DR: Results of this national survey underscore the need to provide physicians with clear guidelines on the use of genetic cancer susceptibility tests and effective medical training on their appropriate implementation.
References
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Journal Article

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

TL;DR: Data from families with evidence of linkage to BRCA1 is used to estimate the age-specific risks of breast and ovarian cancer in BRCa1-mutation carriers and to examine the variation in risk between and within families.
Journal Article

Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence.

TL;DR: The results suggest that the majority of breast cancer families with less than four cases and no ovarian cancer are not due to rare highly penetrant genes such as BRCA1 but are more likely to be due either to chance or to more common genes of lower penetrance.
Journal ArticleDOI

Attitudes about genetic testing for breast-ovarian cancer susceptibility.

TL;DR: The results suggest that the demand for genetic testing for BRCA1 among FDRs of cancer patients may be great, and those who elect to participate may represent a more psychologically vulnerable subgroup of high-risk women.
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