TY - JOUR
T1 - Estimating age-specific breast cancer risks
T2 - A descriptive tool to identify age interactions
AU - Anderson, William F.
AU - Matsuno, Rayna K.
AU - Sherman, Mark E.
AU - Lissowska, Jolanta
AU - Gail, Mitchell H.
AU - Brinton, Louise A.
AU - Yang, Xiaohong
AU - Peplonska, Beata
AU - Chen, Bingshu E.
AU - Rosenberg, Philip S.
AU - Chatterjee, Nilanjan
AU - Szeszenia-Da̧browska, Neonila
AU - Bardin-Mikolajczak, Alicja
AU - Zatonski, Witold
AU - Devesa, Susan S.
AU - García-Closas, Montserrat
N1 - Funding Information:
Acknowledgments This research was supported in part by the Intramural Research Program of the NIH/National Cancer Institute
PY - 2007/5
Y1 - 2007/5
N2 - Objective: Clarifying age-specific female breast cancer risks and interactions may provide important etiologic clues. Method: Using a population-based case-control study in Poland (2000-2003) of 2,386 incident breast cancer cases and 2,502 control subjects aged 25-74 years, we estimated age-specific breast cancer incidence rates according to risk factors. Results: Breast cancer risks were elevated among women with positive family history (FH), younger age at menarche, older age at first full-term birth, nulliparity, exogenous hormonal usage, and reduced physical activity (PA). Notwithstanding overall risks, we observed statistically significant quantitative (non-crossover) and qualitative (crossover) age interactions for all risk factors except for FH and PA. For example, nulliparity compared to parity reduced breast cancer risk among women ages 25-39 years then rates crossed or reversed, after which nulliparity increased relative risks among women ages 40-74 years. Conclusion: Though quantitative age interactions could be expected, qualitative interactions were somewhat counterintuitive. If confirmed in other populations, qualitative interactions for a continuous covariate such as age will be difficult to reconcile in a sequential (multistep or monolithic) 'stochastic' breast cancer model. Alternatively, the reversal of relative risks among younger and older women suggests subgroup heterogeneity with different etiologic mechanisms for early-onset and late-onset breast cancer types.
AB - Objective: Clarifying age-specific female breast cancer risks and interactions may provide important etiologic clues. Method: Using a population-based case-control study in Poland (2000-2003) of 2,386 incident breast cancer cases and 2,502 control subjects aged 25-74 years, we estimated age-specific breast cancer incidence rates according to risk factors. Results: Breast cancer risks were elevated among women with positive family history (FH), younger age at menarche, older age at first full-term birth, nulliparity, exogenous hormonal usage, and reduced physical activity (PA). Notwithstanding overall risks, we observed statistically significant quantitative (non-crossover) and qualitative (crossover) age interactions for all risk factors except for FH and PA. For example, nulliparity compared to parity reduced breast cancer risk among women ages 25-39 years then rates crossed or reversed, after which nulliparity increased relative risks among women ages 40-74 years. Conclusion: Though quantitative age interactions could be expected, qualitative interactions were somewhat counterintuitive. If confirmed in other populations, qualitative interactions for a continuous covariate such as age will be difficult to reconcile in a sequential (multistep or monolithic) 'stochastic' breast cancer model. Alternatively, the reversal of relative risks among younger and older women suggests subgroup heterogeneity with different etiologic mechanisms for early-onset and late-onset breast cancer types.
KW - Absolute risks
KW - Odds ratio
KW - Population-based case-control study
KW - Rate ratios
KW - Relative risks
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U2 - 10.1007/s10552-006-0092-9
DO - 10.1007/s10552-006-0092-9
M3 - Article
C2 - 17216325
AN - SCOPUS:33947219088
SN - 0957-5243
VL - 18
SP - 439
EP - 447
JO - Cancer Causes and Control
JF - Cancer Causes and Control
IS - 4
ER -