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A detailed
family-history can help identify women with gene mutations that
increase the risk of breast cancer, according to a study reported
in the March 29 issue of the Lancet.
Women who carry mutations of BRCA1 and/or BRCA2 genes have up
to an 80 percent higher lifetime risk of breast cancer. A family
history of breast cancer can be an indication that women carry
these genetic mutations, according to researchers at St. Mary's
Hospital in Manchester, England.
The researchers
assessed BRCA1/BRCA2 status and detailed family history for young
English women aged 30 years or younger. About a third of the women
assessed had a strong family history of breast cancer and/or ovarian
cancer. Forty-four percent of the women with a family history
had mutations of BRCA1 or BRCA2 compared with only 6 percent of
women without a family history of breast cancer.
Study author
Dr. Fiona Lalloo said the findings underline the importance of
knowing the family histories of young women diagnosed with breast
cancer for the prediction of mutations in genes such as BRCA1
and BRCA2.
"We recommend
that all breast-cancer surgical notes include a section on family
history, which has to be completed," Lalloo said.
Other
sources: Lancet
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