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Urinary Estrogens and Estrogen Metabolites and Subsequent Risk of Breast Cancer among Premenopausal Women

  1. Author:
    Eliassen, A. H.
    Spiegelman, D.
    Xu, X.
    Keefer, L. K.
    Veenstra, T. D.
    Barbieri, R. L.
    Willett, W. C.
    Hankinson, S. E.
    Ziegler, R. G.
  2. Author Address

    [Eliassen, A. Heather; Willett, Walter C.; Hankinson, Susan E.] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA 02115 USA. [Barbieri, Robert L.] Brigham & Womens Hosp, Dept Obstet Gynecol & Reprod Biol, Boston, MA 02115 USA. [Eliassen, A. Heather; Spiegelman, Donna; Willett, Walter C.; Hankinson, Susan E.] Harvard Univ, Sch Med, Dept Epidemiol, Boston, MA USA. [Spiegelman, Donna] Harvard Univ, Sch Med, Dept Biostat, Boston, MA USA. [Willett, Walter C.] Harvard Univ, Sch Med, Dept Nutr, Boston, MA USA. [Xu, Xia; Veenstra, Timothy D.] NCI, Lab Prote & Analyt Technol, Adv Technol Program, SAIC Frederick Inc, Frederick, MD 21701 USA. [Hankinson, Susan E.] Univ Massachusetts, Sch Publ Hlth & Hlth Sci, Div Biostat & Epidemiol, Amherst, MA 01003 USA. [Keefer, Larry K.] NCI, Comparat Carcinogenesis Lab, Ctr Canc Res, Bethesda, MD 20892 USA. [Ziegler, Regina G.] NCI, Epidemiol & Biostat Program, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA.;Eliassen, AH (reprint author), Brigham & Womens Hosp, Channing Lab, Dept Med, 181 Longwood Ave, Boston, MA 02115 USA;heather.eliassen@channing.harvard.edu
    1. Year: 2012
    2. Date: Feb
  1. Journal: Cancer Research
    1. 72
    2. 3
    3. Pages: 696-706
  2. Type of Article: Article
  3. ISSN: 0008-5472
  1. Abstract:

    Endogenous estrogens and estrogen metabolism are hypothesized to be associated with premenopausal breast cancer risk but evidence is limited. We examined 15 urinary estrogens/estrogen metabolites and breast cancer risk among premenopausal women in a case-control study nested within the Nurses' Health Study II (NHSII). From 1996 to 1999, urine was collected from 18,521 women during the mid-luteal menstrual phase. Breast cancer cases (N = 247) diagnosed between collection and June 2005 were matched to two controls each (N = 485). Urinary estrogen metabolites were measured by liquid chromatography-tandem mass spectrometry and adjusted for creatinine level. Relative risks (RR) and 95% confidence intervals (CI) were estimated by multivariate conditional logistic regression. Higher urinary estrone and estradiol levels were strongly significantly associated with lower risk (top vs. bottom quartile RR: estrone = 0.52; 95% CI, 0.30-0.88; estradiol = 0.51; 95% CI, 0.30-0.86). Generally inverse, although nonsignificant, patterns also were observed with 2- and 4-hydroxylation pathway estrogen metabolites. Inverse associations generally were not observed with 16-pathway estrogen metabolites and a significant positive association was observed with 17-epiestriol (top vs. bottom quartile RR 1.74; 95% CI, 1.08-2.81; P-trend = 0.01). In addition, there was a significant increased risk with higher 16-pathway/parent estrogen metabolite ratio (comparable RR 1.61; 95% CI, 0.99-2.62; P-trend = 0.04). Other pathway ratios were not significantly associated with risk except parent estrogen metabolites/non-parent estrogen metabolites (comparable RR 0.58; 95% CI, 0.35-0.96; P-trend = 0.03). These data suggest that most mid-luteal urinary estrogen metabolite concentrations are not positively associated with breast cancer risk among premenopausal women. The inverse associations with parent estrogen metabolites and the parent estrogen metabolite/non-parent estrogen metabolite ratio suggest that women with higher urinary excretion of parent estrogens are at lower risk. Cancer Res; 72(3); 696-706. (C) 2011 AACR.

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External Sources

  1. DOI: 10.1158/0008-5472.can-11-2507
  2. WOS: 000300405900014

Library Notes

  1. Fiscal Year: FY2011-2012
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