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Postmenopausal Endogenous Hormones Influence Endometrial Cancer Risk

4 February 2004

NEW YORK (Reuters Health) Feb 04 - Pooled prospective data from three cohorts indicate that high levels of endogenous estrogens and androgens significantly raise the risk of endometrial cancer in postmenopausal women, while sex-hormone binding globulin (SHBG) levels are inversely related to endometrial cancer risk.

Dr. Anne Zeleniuch-Jacquotte from New York University School of Medicine and colleagues report these findings in the January 20th issue of The International Journal of Cancer.

"It has long been known that unopposed exogenous estrogens, such as estrogen replacement therapy without the addition of a progesterone, increase the risk of endometrial cancer," Dr. Zeleniuch-Jacquotte noted in comments to Reuters Health.

In the current study, she and her colleagues looked for associations between pre-diagnostic blood concentrations of estradiol, estrone, testosterone, androstenedione, dehydroepiandrosterone sulfate (DHEAS) and SHBG and endometrial cancer risk in 124 women with invasive endometrial cancer, each of whom were matched to two controls. None of the women were taking exogenous hormones at the time of blood collection.

They found that women whose postmenopausal levels of endogenous estradiol were in the top quartile had an adjusted odds ratio for endometrial cancer of 4.13, compared with women whose estradiol levels were in the bottom quartile.

For estrone, androstenedione, testosterone, DHEAS, and SHBG, the adjusted odds ratios were 3.67, 2.15, 1.74, 2.90, and 0.46, respectively, for the highest relative to the lowest levels.

Dr. Zeleniuch-Jacquotte pointed out that "in postmenopausal women, the main source of estrogens is the conversion of androgens to estrogens in adipose tissue. Therefore, levels of circulating estrogens are positively correlated with body mass index."

"The take home message in my opinion," she said, "is that avoiding obesity and weight gain after menopause is expected to reduce the risk of endometrial cancer."

Int J Cancer 2004;108:425-432.

 
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