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ABSTRACT: Interactions between genetic and reproductive factors
in breast cancer risk in a population-based sample of African-American
families
Incidence of breast cancer (BC) varies among ethnic
groups, with higher rates in white than in African-American
women. Until now, most epidemiological and genetic studies have
been carried out in white women.
To investigate whether interactions
between genetic and reproductive risk factors may explain part
of the ethnic disparity in BC incidence, a genetic epidemiology
study was conducted, between 1989 and 1994, at the Howard University
Cancer Center (Washington, DC), which led to the recruitment
of 245 African-American families. Segregation analysis of BC
was performed by use of the class D regressive logistic model
that allows for censored data to account for a variable age of
onset of disease, as implemented in the REGRESS program.
Segregation
analysis of BC was consistent with a putative dominant gene effect
(P < 0.000001) and residual sister-dependence (P < 0.0001).
This putative gene was found to interact significantly with age
at menarche (P = 0.048), and an interaction with a history of
spontaneous abortions was suggested (P = 0.08).
A late age at
menarche increased BC risk in gene carriers but had a protective
effect in non-gene carriers. A history of spontaneous abortions
had a protective effect in gene carriers and increased BC risk
in non-gene carriers.
Our findings agree partially with a similar
analysis of French families showing a significant gene times parity
interaction and a suggestive gene times age at menarche interaction.
Investigating gene times risk factor interactions in different populations
may have important implications for further biological investigations
and for BC risk assessment.
[05/30/2002; Genetic Epidemiology]
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