In a study of the maternity records of more than 6,000 women, David J.P.
Barker, M.D., Ph.D., and Kent Thornburg, Ph.D., of Oregon Health & Science
University discovered a strong correlation between the size and shape of a
woman’s hips and her daughter’s risk of breast cancer. Wide, round hips, the
researchers postulated, represent markers of high sex hormone concentrations
in the mother, which increase her daughter’s vulnerability to breast cancer.
A woman’s hips are shaped at puberty when the growth of the hip bones is
controlled by sex hormones but is also influenced by the level of nutrition.
Every woman has a unique sex hormone profile which is established at puberty
and persists through her reproductive life.
The study’s findings show for the first time that the pubertal growth spurt
of girls is strongly associated with the risk of breast cancer in their
daughters.
The study, carried out with colleagues in Finland and the United Kingdom.,
is described in an article just published online by the peer-reviewed
American Journal of Human Biology. The authors followed up on 6,370 women
born in Helsinki from 1934 to 1944 whose mothers’ pelvic bones were measured
during routine prenatal care. The study found that breast cancer rates were
more than three times higher among the women in the cohort, born at or after
term, whose mothers had wide hips. They were more than seven times higher if
those mothers had already given birth to one or more children.
A woman’s vulnerability to breast cancer, the study found, was greater if
her mother’s “intercristal diameter” – the widest distance between the
wing-like structures at the top of the hip bone – was more than 30
centimeters, or 11.8 inches. The risk also was higher if these wing-like
structures were round. The breast cancer risk was 2.5 times higher for the
daughters of women in whom the widest distance was more than 3 centimeters
greater than the distance at the front.
Barker, professor of medicine (cardiovascular medicine) in the OHSU School
of Medicine as well as professor of clinical epidemiology at the University
of Southampton in the U.K., is internationally known for discovering the
relationship between low birth weight and the lifetime risk for coronary
heart disease and other medical disorders, which the British Medical Journal
has named the Barker Hypothesis. He has published more than 200 papers and
written or edited five books about the developmental origins of chronic
disease. He was honored in 2005 with the prestigious Danone International
Prize for Nutrition for his pioneering research.
The OHSU study published today proposes that breast cancer is initiated in
the first trimester of a pregnancy by exposure of the embryo’s developing
breast tissue to the mother’s circulating sex hormones. The primary mammary
cord, which gives rise to milk-producing breast lobules, develops in the
fetus at 10 weeks. The fetal breast is known to be stimulated by circulating
hormones; the intensity of the stimulation is such that half of all newborn
babies have breast secretions.
“Our findings support the hypothesis that wide round hips reflect high
levels of sex hormone production at puberty, which persist after puberty and
adversely affect breast development of the daughters in early gestation,”
the authors commented. They could only speculate, they said, on the exact
nature of this adverse effect but pointed out: “Catechol estrogen, a
metabolite or estradiol, is thought to cause chromosomal instability by
breaking DNA strands. High catechol estrogen concentrations in the maternal
circulation could produce genetic instability in differentiating breast
epithelial cells, which would make the breast vulnerable to cancer in later
life.”
“Epidemiological findings of this kind aren’t designed to define precise
biological or molecular mechanisms,” said Grover Bagby, M.D., deputy
director of the OHSU Cancer Institute. “However, for those of us involved in
identifying the earliest molecular causes of cancer, these fascinating
results define the types of questions we need to ask. This is a wake-up call
telling us to pay attention to stem cell populations at the time of birth …
a good deal earlier than we might have otherwise done. It is important to
consider these cell populations because only by understanding the initial
cause can we begin to develop rational strategies to prevent this very
common cancer.”
The daughters who were the subjects of the study were all born during
1934-1944 at either Helsinki University Central Hospital or City Maternity
Hospital, the two maternity hospitals in Finland’s capital. The occurrence
of breast cancer among them was ascertained from national registers of all
hospital admissions and deaths in Finland. Three hundred of them had had
breast cancer of whom 48 died from the disease. Their mean age when they
were diagnosed was 54.
The findings shed new light on the link between breast cancer and nutrition.
“Mothers whose daughters developed breast cancer were of similar height to
the other mothers,” Barker and Thornburg reported. “This suggests that they
had similar nutrition through childhood. Our findings do not therefore
indicate that good nutrition through childhood is linked to breast cancer in
the next generation. But they do show that the pubertal growth spurt of
girls, which reflects the level of nutrition, is strongly associated with
the risk of breast cancer in their daughters.”