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https://doi.org/10.1186/s13058-015-0625-9
Title: | A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density | Authors: | Rudolph, A Fasching, P.A Behrens, S |
Keywords: | cytochrome P450 1A1 cytochrome P450 1A2 cytochrome P450 1B1 peroxisome proliferator activated receptor gamma prolactin sulfotransferase 1A1 tumor necrosis factor adult aged AKR1C4 gene Article breast cancer breast density cancer risk case control study controlled study CYP1A1 gene CYP1A2 gene CYP1B1 gene ESR2 gene female gene genetic variability genotype environment interaction hormonal therapy human menopausal hormone therapy PLCG2 gene postmenopause PPARG gene PRL gene single nucleotide polymorphism SULT1A1 gene SULT1A2 gene TNF gene abnormalities breast breast density breast tumor genetics genome-wide association study hormone substitution mammary gland mammography meta analysis middle aged pathology procedures risk factor very elderly Aged Aged, 80 and over Breast Breast Density Breast Neoplasms Case-Control Studies Female Genome-Wide Association Study Hormone Replacement Therapy Humans Mammary Glands, Human Mammography Middle Aged Polymorphism, Single Nucleotide Postmenopause Risk Factors |
Issue Date: | 2015 | Citation: | Rudolph, A, Fasching, P.A, Behrens, S (2015). A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density. Breast Cancer Research 17 (1) : 110. ScholarBank@NUS Repository. https://doi.org/10.1186/s13058-015-0625-9 | Rights: | Attribution 4.0 International | Abstract: | Introduction: Mammographic density is an established breast cancer risk factor with a strong genetic component and can be increased in women using menopausal hormone therapy (MHT). Here, we aimed to identify genetic variants that may modify the association between MHT use and mammographic density. Methods: The study comprised 6,298 postmenopausal women from the Mayo Mammography Health Study and nine studies included in the Breast Cancer Association Consortium. We selected for evaluation 1327 single nucleotide polymorphisms (SNPs) showing the lowest P-values for interaction (P int) in a meta-analysis of genome-wide gene-environment interaction studies with MHT use on risk of breast cancer, 2541 SNPs in candidate genes (AKR1C4, CYP1A1-CYP1A2, CYP1B1, ESR2, PPARG, PRL, SULT1A1-SULT1A2 and TNF) and ten SNPs (AREG-rs10034692, PRDM6-rs186749, ESR1-rs12665607, ZNF365-rs10995190, 8p11.23-rs7816345, LSP1-rs3817198, IGF1-rs703556, 12q24-rs1265507, TMEM184B-rs7289126, and SGSM3-rs17001868) associated with mammographic density in genome-wide studies. We used multiple linear regression models adjusted for potential confounders to evaluate interactions between SNPs and current use of MHT on mammographic density. Results: No significant interactions were identified after adjustment for multiple testing. The strongest SNP-MHT interaction (unadjusted P int <0.0004) was observed with rs9358531 6.5kb 5' of PRL. Furthermore, three SNPs in PLCG2 that had previously been shown to modify the association of MHT use with breast cancer risk were found to modify also the association of MHT use with mammographic density (unadjusted P int <0.002), but solely among cases (unadjusted P int SNP×MHT×case-status <0.02). Conclusions: The study identified potential interactions on mammographic density between current use of MHT and SNPs near PRL and in PLCG2, which require confirmation. Given the moderate size of the interactions observed, larger studies are needed to identify genetic modifiers of the association of MHT use with mammographic density. © 2015 Rudolph et al. | Source Title: | Breast Cancer Research | URI: | https://scholarbank.nus.edu.sg/handle/10635/183752 | ISSN: | 14655411 | DOI: | 10.1186/s13058-015-0625-9 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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