Adiposity and breast, endometrial, and colorectal cancer risk in postmenopausal women: Quantification of the mediating effects of leptin, C-reactive protein, fasting insulin, and estradiol
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Dashti, S.G.Simpson, J.A.
Viallon, V.
Karahalios, A.
Moreno-Betancur, M.
Brasky, T.
Pan, K.
Rohan, T.E.
Shadyab, A.H.
Thomson, C.A.
Wild, R.A.
Wassertheil-Smoller, S.
Ho, G.Y.F.
Strickler, H.D.
English, D.R.
Gunter, M.J.
Affiliation
Health Promotion Sciences, Mel & Enid Zickerman College of Public Health, University of Arizona Cancer CenterIssue Date
2022
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John Wiley and Sons IncCitation
Dashti, S. G., Simpson, J. A., Viallon, V., Karahalios, A., Moreno-Betancur, M., Brasky, T., Pan, K., Rohan, T. E., Shadyab, A. H., Thomson, C. A., Wild, R. A., Wassertheil-Smoller, S., Ho, G. Y. F., Strickler, H. D., English, D. R., & Gunter, M. J. (2022). Adiposity and breast, endometrial, and colorectal cancer risk in postmenopausal women: Quantification of the mediating effects of leptin, C-reactive protein, fasting insulin, and estradiol. Cancer Medicine.Journal
Cancer MedicineRights
Copyright © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Mechanisms underlying the adiposity–cancer relationship are incompletely understood. We quantified the mediating roles of C-reactive protein (CRP), leptin, fasting insulin, and estradiol in the effect of adiposity on estrogen receptor (ER)-positive breast, endometrial, and colorectal cancer risk in postmenopausal women. Methods: We used a case–cohort study within the Women's Health Initiative Observational Study, analyzed as a cumulative sampling case–control study. The study included 188 breast cancer cases, 98 endometrial cancer cases, 193 colorectal cancer cases, and 285 controls. Interventional indirect and direct effects on the risk ratio (RR) scale were estimated using causal mediation analysis. Results: For breast cancer, the total effect RR for BMI ≥30 versus ≥18.5–<25 kg/m2 was 1.87 (95%CI,1.11–3.13). The indirect effect RRs were 1.38 (0.79–2.33) through leptin and CRP, 1.58 (1.17–2.43) through insulin, and 1.11 (0.98–1.30) through estradiol. The direct effect RR was 0.82 (0.39–1.68). For endometrial cancer, the total effect RR was 2.12 (1.12–4.00). The indirect effect RRs were 1.72 (0.85–3.98) through leptin and CRP, 1.42 (0.96–2.26) through insulin, and 1.24 (1.03–1.65) through estradiol. The direct effect RR was 0.70 (0.23–2.04). For colorectal cancer, the total effect RR was 1.70 (1.03–2.79). The indirect effect RRs were 1.04 (0.61–1.72) through leptin and CRP, 1.36 (1.00–1.88) through insulin, and 1.02 (0.88–1.17) through estradiol. The direct effect RR was 1.16 (0.58–2.43). Conclusion: Leptin, CRP, fasting insulin, and estradiol appear to mediate the effect of high BMI on cancer risk to different extents, with likely varying degrees of importance between cancers. These insights might be important in developing interventions to modify obesity-associated cancer risk in postmenopausal women. © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.Note
Open access journalISSN
2045-7634Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1002/cam4.4434
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Except where otherwise noted, this item's license is described as Copyright © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.

