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Adiposity and estrogen receptor-positive,postmenopausal breast cancer risk: Quantification of the mediating effects of fasting insulin and free estradiol
Authors:S. Ghazaleh Dashti  Julie A. Simpson  Amalia Karahalios  Vivian Viallon  Margarita Moreno-Betancur  Lyle C. Gurrin  Robert J. MacInnis  Brigid M. Lynch  Laura Baglietto  Howard A. Morris  Marc J. Gunter  Pietro Ferrari  Roger L. Milne  Graham G. Giles  Dallas R. English
Affiliation:1. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia;2. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia

School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia;3. Section of Nutrition and Metabolism, International Agency for Research on Cancer (IARC), Lyon, France;4. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia

Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Melbourne, VIC, Australia;5. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia

Cancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, VIC, Australia;6. Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia

Cancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, VIC, Australia

Physical Activity Laboratory, Baker Heart and Diabetes Institute, Melbourne, VIC, Australia;7. Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

Abstract:Adiposity increases estrogen receptor (ER)-positive postmenopausal breast cancer risk. While mechanisms underlying this relationship are uncertain, dysregulated sex-steroid hormone production and insulin signaling are likely pathways. Our aim was to quantify mediating effects of fasting insulin and free estradiol in the adiposity and ER-positive postmenopausal breast cancer association. We used data from a case–cohort study of sex hormones and insulin signaling nested within the Melbourne Collaborative Cohort Study. Eligible women, at baseline, were not diagnosed with cancer, were postmenopausal, did not use hormone therapy and had no history of diabetes or diabetes medication use. Women with ER-negative disease or breast cancer diagnosis within the first follow-up year were excluded. We analyzed the study as a cumulative sampling case–control study with 149 cases and 1,029 controls. Missing values for insulin and free estradiol were multiply imputed with chained equations. Interventional direct (IDE) and indirect (IIE) effects were estimated using regression-based multiple-mediator approach. For women with body mass index (BMI) >30 kg/m2 compared to women with BMI 18.5–25 kg/m2, the risk ratio (RR) of breast cancer was 1.75 (95% confidence interval [CI] 1.05–2.91). The estimated IDE (RR) not through the mediators was 1.03 (95% CI 0.43–2.48). Percentage mediated effect through free estradiol was 72% (IIE-RR 1.56; 95% CI 1.11–2.19). There was no evidence for an indirect effect through insulin (IIE-RR 1.12; 95% CI 0.68–1.84; 28% mediated). Our results suggest that circulating free estradiol plays an important mediating role in the adiposity–breast cancer relationship but does not explain all of the association.
Keywords:adiposity  estrogen receptor-positive  postmenopausal breast cancer  causal mediation analysis  insulin  estrogens  free estradiol  circulating estrogens
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