Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

Aging Epidemiology Gene-environment interactions Medical Genetics and Genomics Body Mass Index Breast cancer 0302 clinical medicine Risk Factors Receptors 80 and over 2.1 Biological and endogenous factors /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being; name=SDG 3 - Good Health and Well-being Aetiology Medical History Taking Cancer Aged, 80 and over Single Nucleotide Middle Aged Medicinsk genetik och genomik Risk prediction 3. Good health Receptors, Estrogen /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being Female Medical Genetics kConFab/AOCS Investigators Oncology and Carcinogenesis ABCTB Investigators 610 Breast Neoplasms Brief Communication Polymorphism, Single Nucleotide White People Breast cancer; Epidemiology; Gene-environment interactions; Genetic susceptibility; Polygenic risk score; Risk factors; Risk prediction 03 medical and health sciences Polygenic risk score Clinical Research Breast Cancer Genetic susceptibility Humans Genetic Predisposition to Disease Oncology & Carcinogenesis Polymorphism Medicinsk genetik Aged Cancer och onkologi Prevention Estrogen name=SDG 3 - Good Health and Well-being Logistic Models Risk factors Cancer and Oncology Case-Control Studies
DOI: 10.1093/jnci/djaa056 Publication Date: 2020-04-23T19:09:31Z
AUTHORS (142)
ABSTRACT
Abstract We evaluated the joint associations between a new 313-variant PRS (PRS313) and questionnaire-based breast cancer risk factors for women of European ancestry, using 72 284 cases and 80 354 controls from the Breast Cancer Association Consortium. Interactions were evaluated using standard logistic regression and a newly developed case-only method for breast cancer risk overall and by estrogen receptor status. After accounting for multiple testing, we did not find evidence that per-standard deviation PRS313 odds ratio differed across strata defined by individual risk factors. Goodness-of-fit tests did not reject the assumption of a multiplicative model between PRS313 and each risk factor. Variation in projected absolute lifetime risk of breast cancer associated with classical risk factors was greater for women with higher genetic risk (PRS313 and family history) and, on average, 17.5% higher in the highest vs lowest deciles of genetic risk. These findings have implications for risk prevention for women at increased risk of breast cancer.
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