Premenopausal Circulating Androgens and Risk of Endometrial Cancer: results of a Prospective Study

被引:24
作者
Clendenen, Tess V. [1 ]
Hertzmark, Kathryn [2 ]
Koenig, Karen L. [1 ]
Lundin, Eva [3 ]
Rinaldi, Sabina [4 ]
Johnson, Theron [5 ]
Krogh, Vittorio [6 ]
Hallmans, Goran [7 ,8 ]
Idahl, Annika [9 ]
Lukanova, Annekatrin [5 ]
Zeleniuch-Jacquotte, Anne [1 ,10 ]
机构
[1] NYU, Sch Med, Dept Populat Hlth, Div Epidemiol & Biostat, 650 1st Ave, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Environm Med, Div Epidemiol & Biostat, New York, NY 10016 USA
[3] Umea Univ, Dept Med Biosci, Pathol, Umea, Sweden
[4] Int Agcy Res Canc, 150 Cours Albert Thomas, F-69372 Lyon, France
[5] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[6] Fdn IRCCS Ist Nazl Tumori, Epidemiol & Prevent Unit, Milan, Italy
[7] Umea Univ, Dept Publ Hlth & Clin Med Nutr Res, Umea, Sweden
[8] Umea Univ, Dept Biobank Res, Umea, Sweden
[9] Umea Univ, Dept Clin Sci Obstet & Gynecol, Umea, Sweden
[10] NYU, Inst Canc, New York, NY 10016 USA
来源
HORMONES & CANCER | 2016年 / 7卷 / 03期
关键词
POLYCYSTIC-OVARY-SYNDROME; STEROID-HORMONES; SERUM TESTOSTERONE; GENITAL-TRACT; WOMEN; ESTROGENS; GROWTH; ANDROSTENEDIONE; PREVALENCE; VALIDITY;
D O I
10.1007/s12672-016-0258-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endometrial cancer risk is increased by estrogens unopposed by progesterone. In premenopausal women, androgen excess is often associated with progesterone insufficiency, suggesting that premenopausal androgen concentrations may be associated with risk. In a case-control study nested within three cohorts, we assessed the relationship between premenopausal androgens and risk of endometrial cancer (161 cases and 303 controls matched on age and date of blood donation). Testosterone, DHEAS, androstenedione, and SHBG were measured in serum or plasma. Free testosterone was calculated from testosterone and SHBG. We observed trends of increasing risk across tertiles of testosterone (ORT3-T1 = 1.59, 95 % CI = 0.96, 2.64, p = 0.08) and free testosterone (ORT3-T1 = 1.76, 95 % CI = 1.01, 3.07, p = 0.047), which were not statistically significant after adjustment for body mass index (BMI). There was no association for DHEAS, androstenedione, or SHBG. There were significant interactions by age at diagnosis (<55 years, n = 51 cases; >= 55 years, n = 110 cases). Among women who were >= 55 years of age (predominantly postmenopausal) at diagnosis, the BMI-adjusted OR was 2.08 (95 % CI = 1.25, 3.44, p = 0.005) for a doubling in testosterone and 1.55 (95 % CI = 1.04, 2.31, p = 0.049) for a doubling in free testosterone. There was no association among women aged <55 years at diagnosis, consistent with the only other prospective study to date. If pre- and post-menopausal concentrations of androgens are correlated, our observation of an association of premenopausal androgens with risk among women aged >= 55 years at diagnosis could be due to the effect on the endometrium of postmenopausal androgen-derived estrogens in the absence of progesterone, which is no longer secreted.
引用
收藏
页码:178 / 187
页数:10
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