TUESDAY, June 1 (HealthDay News) -- Despite prior research
identifying both genetic risks for breast cancer as well as risks
associated with lifestyle and environmental factors, a new British study
reveals that the two types of risk pools appear to operate independently
of one another.
The finding is based on analysis that looked for any evidence of an
interaction between a dozen genetic mutations -- all associated with a
small increase in breast cancer risk -- and 10 established environmental
risk factors, which are factors linked to behavior or lifestyle. The
results are reported in the June 2 online edition of The
Lancet.
"We looked at whether lifestyle factors for breast cancer, such as use
of HRT [hormone replacement therapy], alcohol consumption and reproductive
history, influence the genetic risks," study author Dr. Ruth Travis, of
the cancer epidemiology unit at the University of Oxford in the United
Kingdom, said in a news release. "And the answer is that they do not."
Travis and her colleagues focused on 7,610 women who had been diagnosed
with breast cancer, as well as nearly 10,200 women who did not have the
disease. All of the women provided blood samples for genetic testing, as
well as detailed information concerning their lifestyles.
DNA analyses looked for 12 common genetic variables, while the authors
sifted through the collected lifestyle information in search of a specific
group of environmental risk factors: age at first menstruation; number of
births; age of mother at first birth; breast-feeding patterns; menopausal
status; age at menopause; use of hormone replacement therapy; body-mass
index; height; and alcohol consumption history.
Genetic risks and environmental risks did not appear to interact. In
particular, the research team noted that despite previous indications to
the contrary, hormone replacement therapy did not appear to have any
significant impact on genetic risk factors.
More information
For more on breast cancer risk, visit the American Cancer Society.
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