Circulating levels of sex steroid hormones and risk of endometrial cancer in postmenopausal women

Annekatrin Lukanova, Eva Lundin, Andrea Micheli, Alan Arslan, Pietro Ferrari, Sabina Rinaldi, Vittorio Krogh, Per Lenner, Roy E. Shore, Carine Biessy, Paola Muti, Elio Riboli, Karen L. Koenig, Mortimer Levitz, Pär Stattin, Franco Berrino, Göran Hallmans, Rudolf Kaaks, Paolo Toniolo, Anne Zeleniuch-Jacquotte

Research output: Contribution to journalArticlepeer-review


Experimental and epidemiological data support a role for sex steroid hormones in the pathogenesis of endometrial cancer. The associations of pre-diagnostic blood concentrations of estradiol, estrone, testosterone, androstenedione, DHEAS and SHBG with endometrial cancer risk were investigated. A case-control study was nested within 3 cohorts in New York (USA), Umeå (Sweden) and Milan (Italy). Cases were 124 postmenopausal women with invasive endometrial cancer. For each case, 2 controls were selected, matching the case on cohort, age and date of recruitment. Only postmenopausal women who did not use exogenous hormones at the time of blood donation were included. Odds ratios (OR) and their 95% confidence intervals (Cl) were estimated by conditional logistic regression. ORs (95% Cl) for endometrial cancer for quartiles with the highest hormone levels, relative to the lowest were as follows: 4.13 (1.76-9.72), Ptrend = 0.0008 for estradiol, 3.67 (1.71-7.88), P trend = 0.0007 for estrone, 2.15 (1.05-4.40), Ptrend = 0.04 for androstenedione, 1.74 (0.88-3.46), Ptrend = 0.06 for testosterone, 2.90 (1.42-5.90), Ptrend = 0.002 for DHEAS and 0.46 (0.20-1.05), Ptrend = 0.01 for SHBG after adjustment for body mass index, use of oral contraceptives and hormone replacement therapy. The results of our multicenter prospective study showed a strong direct association of circulating estrogens, androgens and an inverse association of SHBG levels with endometrial cancer in postmenopausal women. The effect of elevated androstenedione and testosterone levels on disease risk seems to be mediated mainly through their conversion to estrogens, although an independent effect of androgens on tumor growth cannot be ruled out, in particular in the years close to diagnosis.

Original languageEnglish
Pages (from-to)425-432
Number of pages8
JournalInternational Journal of Cancer
Issue number3
Publication statusPublished - Jan 20 2004


  • Androstenedione
  • Cohort study
  • Endometrial cancer
  • Estradiol
  • Estrone
  • SHBG
  • Testosterone

ASJC Scopus subject areas

  • Cancer Research
  • Oncology


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