Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.

Additive interactions can have public health and etiological implications but are infrequently reported. We assessed departures from additivity on the absolute risk scale between 9 established breast cancer risk factors and 23 susceptibility single-nucleotide polymorphisms (SNPs) identified from gen...

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Hoofdauteurs: Joshi, A, Lindström, S, Hüsing, A, Barrdahl, M, VanderWeele, T, Campa, D, Canzian, F, Gaudet, M, Figueroa, J, Baglietto, L, Berg, C, Buring, J, Chanock, S, Chirlaque, MD, Diver, W, Dossus, L, Giles, G, Haiman, C, Hankinson, SE, Henderson, B, Hoover, R, Hunter, D, Isaacs, C, Kaaks, R, Kolonel, L
Formaat: Journal article
Taal:English
Gepubliceerd in: Oxford University Press 2014
_version_ 1826291664253091840
author Joshi, A
Lindström, S
Hüsing, A
Barrdahl, M
VanderWeele, T
Campa, D
Canzian, F
Gaudet, M
Figueroa, J
Baglietto, L
Berg, C
Buring, J
Chanock, S
Chirlaque, MD
Diver, W
Dossus, L
Giles, G
Haiman, C
Hankinson, SE
Henderson, B
Hoover, R
Hunter, D
Isaacs, C
Kaaks, R
Kolonel, L
author_facet Joshi, A
Lindström, S
Hüsing, A
Barrdahl, M
VanderWeele, T
Campa, D
Canzian, F
Gaudet, M
Figueroa, J
Baglietto, L
Berg, C
Buring, J
Chanock, S
Chirlaque, MD
Diver, W
Dossus, L
Giles, G
Haiman, C
Hankinson, SE
Henderson, B
Hoover, R
Hunter, D
Isaacs, C
Kaaks, R
Kolonel, L
author_sort Joshi, A
collection OXFORD
description Additive interactions can have public health and etiological implications but are infrequently reported. We assessed departures from additivity on the absolute risk scale between 9 established breast cancer risk factors and 23 susceptibility single-nucleotide polymorphisms (SNPs) identified from genome-wide association studies among 10,146 non-Hispanic white breast cancer cases and 12,760 controls within the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium. We estimated the relative excess risk due to interaction and its 95% confidence interval for each pairwise combination of SNPs and nongenetic risk factors using age- and cohort-adjusted logistic regression models. After correction for multiple comparisons, we identified a statistically significant relative excess risk due to interaction (uncorrected P = 4.51 × 10(-5)) between a SNP in the DNA repair protein RAD51 homolog 2 gene (RAD51L1; rs10483813) and body mass index (weight (kg)/height (m)(2)). We also compared additive and multiplicative polygenic risk prediction models using per-allele odds ratio estimates from previous studies for breast-cancer susceptibility SNPs and observed that the multiplicative model had a substantially better goodness of fit than the additive model.
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spelling oxford-uuid:b1864b8c-c18c-45de-8295-c4e9a68dce6f2022-03-27T04:04:45ZAdditive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b1864b8c-c18c-45de-8295-c4e9a68dce6fEnglishSymplectic Elements at OxfordOxford University Press2014Joshi, ALindström, SHüsing, ABarrdahl, MVanderWeele, TCampa, DCanzian, FGaudet, MFigueroa, JBaglietto, LBerg, CBuring, JChanock, SChirlaque, MDDiver, WDossus, LGiles, GHaiman, CHankinson, SEHenderson, BHoover, RHunter, DIsaacs, CKaaks, RKolonel, LAdditive interactions can have public health and etiological implications but are infrequently reported. We assessed departures from additivity on the absolute risk scale between 9 established breast cancer risk factors and 23 susceptibility single-nucleotide polymorphisms (SNPs) identified from genome-wide association studies among 10,146 non-Hispanic white breast cancer cases and 12,760 controls within the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium. We estimated the relative excess risk due to interaction and its 95% confidence interval for each pairwise combination of SNPs and nongenetic risk factors using age- and cohort-adjusted logistic regression models. After correction for multiple comparisons, we identified a statistically significant relative excess risk due to interaction (uncorrected P = 4.51 × 10(-5)) between a SNP in the DNA repair protein RAD51 homolog 2 gene (RAD51L1; rs10483813) and body mass index (weight (kg)/height (m)(2)). We also compared additive and multiplicative polygenic risk prediction models using per-allele odds ratio estimates from previous studies for breast-cancer susceptibility SNPs and observed that the multiplicative model had a substantially better goodness of fit than the additive model.
spellingShingle Joshi, A
Lindström, S
Hüsing, A
Barrdahl, M
VanderWeele, T
Campa, D
Canzian, F
Gaudet, M
Figueroa, J
Baglietto, L
Berg, C
Buring, J
Chanock, S
Chirlaque, MD
Diver, W
Dossus, L
Giles, G
Haiman, C
Hankinson, SE
Henderson, B
Hoover, R
Hunter, D
Isaacs, C
Kaaks, R
Kolonel, L
Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title_full Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title_fullStr Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title_full_unstemmed Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title_short Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
title_sort additive interactions between susceptibility single nucleotide polymorphisms identified in genome wide association studies and breast cancer risk factors in the breast and prostate cancer cohort consortium
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