They need to be more aware of the threats to themselves and relatives, study says
FRIDAY, Feb. 27 (HealthDay News) -- Men who are part of families in which some members have BRCA1 or 2 gene mutations -- which boost the risk for breast and ovarian cancer -- typically avoid genetic counseling or testing, a new study found.
When they do get counseling or testing, they're less likely than women to pass on the information or to discuss it thoroughly with their family members, according to study author Dr. Mary Daly, director of the cancer prevention and control program at Fox Chase Cancer Center in Philadelphia.
That's true even though men who carry these mutations "have a 50 percent chance of passing them on to their children," as well as an increased risk for getting certain cancers themselves, Daly said. Most cancers associated with BRCA1 and 2 mutations are seen in women, but men with these mutations are at higher risk for male breast cancer as well as prostate and pancreatic cancer and melanoma, she said.
For instance, a daughter with BRCA1 or 2 mutations has an estimated risk of 56 percent to 87 percent of developing breast cancer by age 70, Daly said, and half of these cancers occur before age 50. The risk is especially high for members of the Ashkenazi Jewish population, in which BRCA mutations have been seen in 2.3 percent of people, she said.
Daly's findings were published in the February issue of the Journal of Genetic Counseling.
Daly, who reviewed several published studies for her report, decided to do the research after finding that men typically weren't interested in getting genetic counseling or testing, even when family members tested positive for genetic mutations.
"In our experience, counseling family members [with genetic mutations], we deal primarily with women," she said.
Many men are simply unaware of how genetic mutations in the family can affect t
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