Urinary Estrogen Metabolites and Long-Term Mortality Following Breast Cancer

Author:

Wang Tengteng123ORCID,Nichols Hazel B1,Nyante Sarah J14,Bradshaw Patrick T5ORCID,Moorman Patricia G6,Kabat Geoffrey C7,Parada Humberto8,Khankari Nikhil K9,Teitelbaum Susan L10,Terry Mary Beth11,Santella Regina M12,Neugut Alfred I1113,Gammon Marilie D1

Affiliation:

1. Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA

2. Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA

3. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA

4. Department of Radiology, University of North Carolina, Chapel Hill, NC, USA

5. Division of Epidemiology, University of California, Berkeley, CA, USA

6. Department of Community and Family Medicine, Duke University, Durham, NC, USA

7. 16 Bon Air Ave, New Rochelle, NY 10804, USA

8. Division of Epidemiology and Biostatistics, San Diego State University, San Diego, CA, USA

9. Division of Epidemiology, Vanderbilt University Medical Center, Nashville, TN, USA

10. Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA

11. Department of Epidemiology, Columbia University, New York, NY, USA

12. Department of Environmental Health Sciences, Columbia University, New York, NY, USA

13. Department of Medicine, Columbia University, New York, NY, USA

Abstract

Abstract Background Estrogen metabolite concentrations of 2-hydroxyestrone (2-OHE1) and 16-hydroxyestrone (16-OHE1) may be associated with breast carcinogenesis. However, no study has investigated their possible impact on mortality after breast cancer. Methods This population-based study was initiated in 1996–1997 with spot urine samples obtained shortly after diagnosis (mean = 96 days) from 683 women newly diagnosed with first primary breast cancer and 434 age-matched women without breast cancer. We measured urinary concentrations of 2-OHE1 and 16-OHE1 using an enzyme-linked immunoassay. Vital status was determined via the National Death Index (n = 244 deaths after a median of 17.7 years of follow-up). We used multivariable-adjusted Cox proportional hazards to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the estrogen metabolites-mortality association. We evaluated effect modification using likelihood ratio tests. All statistical tests were two-sided. Results Urinary concentrations of the 2-OHE1 to 16-OHE1 ratio (>median of 1.8 vs ≤median) were inversely associated with all-cause mortality (HR = 0.74, 95% CI = 0.56 to 0.98) among women with breast cancer. Reduced hazard was also observed for breast cancer mortality (HR = 0.73, 95% CI = 0.45 to 1.17) and cardiovascular diseases mortality (HR = 0.76, 95% CI = 0.47 to 1.23), although the 95% confidence intervals included the null. Similar findings were also observed for women without breast cancer. The association with all-cause mortality was more pronounced among breast cancer participants who began chemotherapy before urine collection (n = 118, HR = 0.42, 95% CI = 0.22 to 0.81) than among those who had not (n = 559, HR = 0.98, 95% CI = 0.72 to 1.34; Pinteraction = .008). Conclusions The urinary 2-OHE1 to 16-OHE1 ratio may be inversely associated with long-term all-cause mortality, which may depend on cancer treatment status at the time of urine collection.

Funder

National Institutes of Health

Babylon Breast Cancer Coalition

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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