Reproductive factors and familial predisposition for breast cancer by age 50 years. A case-control-family study for assessing main effects and possible gene-environment interaction

Int J Epidemiol. 2003 Feb;32(1):38-48. doi: 10.1093/ije/dyg003.

Abstract

Background: The effect of environmental/lifestyle factors on breast cancer risk may be modified by genetic predisposition.

Methods: In a population-based case-control-family study performed in Germany including 706 cases by age 50 years, 1381 population, and 252 sister controls, we investigated main effects for environmental/lifestyle factors and genetic susceptibility and gene-environment interaction (G x E). Different surrogate measures for genetic predisposition using pedigree information were used: first-degree family history of breast or ovarian cancer; and gene carrier probability using a genetic model based on rare dominant genes. Possible G x E interaction was studied by (1) logistic regression using cases and population controls including an interaction term; (2) comparing results using sister controls and population controls; (3) case-only analysis with logistic regression and (4) a mixture logistic model.

Results: Familial predisposition showed the strongest main effect and the estimated gene carrier probability gave the best fit. High parity and longer duration of breastfeeding reduced breast cancer risk significantly, a history of abortions increased risk and age at menarche showed no significant effect. We found significant G x E interaction between parity and genetic susceptibility using different surrogate measures. In women most likely to have a high genetic susceptibility, high parity was less protective. Later age at menarche was protective in women with a positive family history. No evidence for G x E interaction was found for breastfeeding and abortion.

Conclusions: These findings corroborate results from other studies and provide further evidence that the magnitude of protection from parity is reduced in women most likely to have a genetic risk in spite of the limitations of using surrogate genetic measures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortion, Therapeutic
  • Breast Feeding
  • Breast Neoplasms / etiology*
  • Breast Neoplasms / genetics
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Heterozygote
  • Humans
  • Life Style
  • Logistic Models
  • Menarche
  • Middle Aged
  • Parity
  • Reproductive History*
  • Siblings