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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CITATIONS (51)
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