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. 2013 Sep 16;105(19):1496–1503. doi: 10.1093/jnci/djt243

Table 2.

Association of baseline sex hormone levels with invasive breast cancer risk

Sex hormone Number of case subjects, number of control subjects Odds ratio (95% confidence interval)*
Total estradiol†
    Quartile (Q)1 (2.5–7.94) 27, 60 1.00 (referent)
    Q2 (7.95–10.89) 42, 41 2.07 (1.06 to 4.04)
    Q3 (10.90–14.99) 37, 43 1.58 (0.77 to 3.21)
    Q4 (15.00–39.20) 38, 31 2.52 (1.12 to 5.63)
    P trend .04
Bioavailable estradiol†
    Q1 (1.58–4.99) 29, 57 1.00 (referent)
    Q2 (5.00–7.14) 37, 43 1.58 (0.75 to 3.29)
    Q3 (7.15–10.52) 37, 46 1.35 (0.66 to 2.75)
    Q4 (10.53–29.30) 41, 28 2.82 (1.25 to 6.36)
    P trend .03
Estrone†
    Q1 (9.05–27.86) 31, 56 1.00 (referent)
    Q2 (27.87–36.78) 40, 44 1.87 (0.92 to 3.80)
    Q3 (36.79–50.38) 34, 43 2.19 (1.03 to 4.66)
    Q4 (50.39–151.39) 42, 34 3.01 (1.34 to 6.76)
    P trend .007
Estrone sulphate
    Q1 (0.23–0.56) 71, 93 1.00 (referent)
    Q2 (0.57–0.76) 70, 74 1.41 (0.83 to 2.39)
    Q3 (0.77–1.034) 87, 70 2.23 (1.23 to 4.02)
    Q4 (1.035–2.75) 86, 77 2.38 (1.20 to 4.72)
    P trend .007
Progesterone
    Q1 (11.66–40.44) 81, 77 1.00 (referent)
    Q2 (40.45–58.87) 83, 85 0.89 (0.54 to 1.45)
    Q3 (58.87–83.49) 88, 84 0.94 (0.56 to 1.58)
    Q4 (83.50–498.7) 88, 94 0.96 (0.56 to 1.67)
    P trend .96
Total testosterone
    Q1 (3.84–16.59) 64, 71 1.00 (referent)
    Q2 (16.60–22.57) 76, 95 0.84 (0.50 to 1.41)
    Q3 (22.58–31.38) 96, 78 1.34 (0.79 to 2.28)
    Q4 (31.39–118.42) 106, 98 1.08 (0.65 to 1.80)
    P trend .35
Bioavailable testosterone
    Q1 (0.51–8.30) 72, 70 1.00 (referent)
    Q2 (8.31–11.50) 70, 92 0.74 (0.44 to 1.26)
    Q3 (11.51–16.05) 86, 87 1.01 (0.60 to 1.68)
    Q4 (16.06–81.11) 110, 89 1.11 (0.66 to 1.86)
    P trend .38
Sex hormone–binding globulin
    Q1 (6.9–27.89) 80, 77 1.00 (referent)
    Q2 (27.90–39.54) 94, 69 1.45 (0.87 to 2.42)
    Q3 (39.55–54.99) 77, 104 0.79 (0.48 to 1.30)
    Q4 (55.00–159.00) 91, 92 1.05 (0.62 to 1.79)
    P trend .54

* Adjusted for treatment assignment, age at menarche, body mass index, and family history of breast cancer. Results were obtained using conditional logistic regression models. All statistical tests were two-sided.

† Total estradiol, bioavailable estradiol, and estrone estimates were obtained from the placebo group, due to their statistically significant interactions with estrogen + progestin treatment.