Case–control study of endogenous sex steroid hormones and risk of endometrial cancer

Background Epidemiologic evidence regarding the role of endogenous sex hormones in endometrial cancer etiology remains inconsistent. The objective of this study was to investigate if circulating levels of endogenous estrone, estradiol, sex hormone binding globulin (SHBG), testosterone, and androsten...

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Veröffentlicht in:Cancer causes & control 2020-02, Vol.31 (2), p.161-171
Hauptverfasser: Friedenreich, Christine M., Derksen, Jeroen W. G., Speidel, Thomas, Brenner, Darren R., Heer, Emily, Courneya, Kerry S., Cook, Linda S.
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container_end_page 171
container_issue 2
container_start_page 161
container_title Cancer causes & control
container_volume 31
creator Friedenreich, Christine M.
Derksen, Jeroen W. G.
Speidel, Thomas
Brenner, Darren R.
Heer, Emily
Courneya, Kerry S.
Cook, Linda S.
description Background Epidemiologic evidence regarding the role of endogenous sex hormones in endometrial cancer etiology remains inconsistent. The objective of this study was to investigate if circulating levels of endogenous estrone, estradiol, sex hormone binding globulin (SHBG), testosterone, and androstenedione are associated with endometrial cancer risk. Methods We conducted a population-based case–control study of 522 incident endometrial cancer cases and 976 population controls, in Alberta, Canada from 2002 to 2006. Study participants completed in-person interviews and provided fasting blood samples. Sex hormone levels were determined by enzyme-linked immunosorbent assays. Results Higher levels of androstenedione were associated with increased endometrial cancer risk (OR 1.44, 95% CI 1.04–2.02). Endometrial cancer risk in pre- and peri-menopausal women was reduced for the highest versus lowest quartiles of estrone (OR 0.44, 95% CI 0.22–0.88) and estradiol (OR 0.30, 95% CI 0.14–0.65), but in post-menopausal women, the endometrial cancer risk was increased for the highest versus lowest quartile of androstenedione (OR 1.82, 95% CI 1.25–2.65). In addition, endometrial cancer risk in normal/underweight women was decreased for the highest versus lowest quartile of serum SHBG (OR 0.39, 95% CI 0.19–0.84). Conclusions Overall, positive associations were found for androstenedione concentrations, while sub-group analyses revealed = inverse associations with estrogens and SHBG. Results of this study provide empirical evidence for the role of circulating sex hormones in endometrial cancer etiology and highlight the importance of modifiable factors that contribute to changes in sex hormone concentration levels.
doi_str_mv 10.1007/s10552-019-01260-5
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G. ; Speidel, Thomas ; Brenner, Darren R. ; Heer, Emily ; Courneya, Kerry S. ; Cook, Linda S.</creator><creatorcontrib>Friedenreich, Christine M. ; Derksen, Jeroen W. G. ; Speidel, Thomas ; Brenner, Darren R. ; Heer, Emily ; Courneya, Kerry S. ; Cook, Linda S.</creatorcontrib><description>Background Epidemiologic evidence regarding the role of endogenous sex hormones in endometrial cancer etiology remains inconsistent. The objective of this study was to investigate if circulating levels of endogenous estrone, estradiol, sex hormone binding globulin (SHBG), testosterone, and androstenedione are associated with endometrial cancer risk. Methods We conducted a population-based case–control study of 522 incident endometrial cancer cases and 976 population controls, in Alberta, Canada from 2002 to 2006. Study participants completed in-person interviews and provided fasting blood samples. Sex hormone levels were determined by enzyme-linked immunosorbent assays. Results Higher levels of androstenedione were associated with increased endometrial cancer risk (OR 1.44, 95% CI 1.04–2.02). Endometrial cancer risk in pre- and peri-menopausal women was reduced for the highest versus lowest quartiles of estrone (OR 0.44, 95% CI 0.22–0.88) and estradiol (OR 0.30, 95% CI 0.14–0.65), but in post-menopausal women, the endometrial cancer risk was increased for the highest versus lowest quartile of androstenedione (OR 1.82, 95% CI 1.25–2.65). In addition, endometrial cancer risk in normal/underweight women was decreased for the highest versus lowest quartile of serum SHBG (OR 0.39, 95% CI 0.19–0.84). Conclusions Overall, positive associations were found for androstenedione concentrations, while sub-group analyses revealed = inverse associations with estrogens and SHBG. Results of this study provide empirical evidence for the role of circulating sex hormones in endometrial cancer etiology and highlight the importance of modifiable factors that contribute to changes in sex hormone concentration levels.</description><identifier>ISSN: 0957-5243</identifier><identifier>EISSN: 1573-7225</identifier><identifier>DOI: 10.1007/s10552-019-01260-5</identifier><identifier>PMID: 31865473</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>17β-Estradiol ; Aged ; Alberta - epidemiology ; Androstenedione ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Cancer Research ; Case-Control Studies ; Empirical analysis ; Endometrial cancer ; Endometrial Neoplasms - epidemiology ; Endometrium ; Epidemiology ; Estrogens ; Estrone ; Etiology ; Female ; Globulins ; Gonadal Steroid Hormones - blood ; Health risk assessment ; Health risks ; Hematology ; Hormone replacement therapy ; Hormones ; Humans ; Immunoassays ; Menopause ; Middle Aged ; Oncology ; Original Paper ; Population studies ; Post-menopause ; Prospective Studies ; Public Health ; Quartiles ; Risk ; Sex Hormone-Binding Globulin - analysis ; Sex hormones ; Steroid hormones ; Steroids ; Testosterone ; Underweight</subject><ispartof>Cancer causes &amp; control, 2020-02, Vol.31 (2), p.161-171</ispartof><rights>Springer Nature Switzerland AG 2019</rights><rights>Cancer Causes &amp; Control is a copyright of Springer, (2019). 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G.</creatorcontrib><creatorcontrib>Speidel, Thomas</creatorcontrib><creatorcontrib>Brenner, Darren R.</creatorcontrib><creatorcontrib>Heer, Emily</creatorcontrib><creatorcontrib>Courneya, Kerry S.</creatorcontrib><creatorcontrib>Cook, Linda S.</creatorcontrib><title>Case–control study of endogenous sex steroid hormones and risk of endometrial cancer</title><title>Cancer causes &amp; control</title><addtitle>Cancer Causes Control</addtitle><addtitle>Cancer Causes Control</addtitle><description>Background Epidemiologic evidence regarding the role of endogenous sex hormones in endometrial cancer etiology remains inconsistent. The objective of this study was to investigate if circulating levels of endogenous estrone, estradiol, sex hormone binding globulin (SHBG), testosterone, and androstenedione are associated with endometrial cancer risk. Methods We conducted a population-based case–control study of 522 incident endometrial cancer cases and 976 population controls, in Alberta, Canada from 2002 to 2006. Study participants completed in-person interviews and provided fasting blood samples. Sex hormone levels were determined by enzyme-linked immunosorbent assays. Results Higher levels of androstenedione were associated with increased endometrial cancer risk (OR 1.44, 95% CI 1.04–2.02). Endometrial cancer risk in pre- and peri-menopausal women was reduced for the highest versus lowest quartiles of estrone (OR 0.44, 95% CI 0.22–0.88) and estradiol (OR 0.30, 95% CI 0.14–0.65), but in post-menopausal women, the endometrial cancer risk was increased for the highest versus lowest quartile of androstenedione (OR 1.82, 95% CI 1.25–2.65). In addition, endometrial cancer risk in normal/underweight women was decreased for the highest versus lowest quartile of serum SHBG (OR 0.39, 95% CI 0.19–0.84). Conclusions Overall, positive associations were found for androstenedione concentrations, while sub-group analyses revealed = inverse associations with estrogens and SHBG. 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G.</au><au>Speidel, Thomas</au><au>Brenner, Darren R.</au><au>Heer, Emily</au><au>Courneya, Kerry S.</au><au>Cook, Linda S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Case–control study of endogenous sex steroid hormones and risk of endometrial cancer</atitle><jtitle>Cancer causes &amp; control</jtitle><stitle>Cancer Causes Control</stitle><addtitle>Cancer Causes Control</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>31</volume><issue>2</issue><spage>161</spage><epage>171</epage><pages>161-171</pages><issn>0957-5243</issn><eissn>1573-7225</eissn><abstract>Background Epidemiologic evidence regarding the role of endogenous sex hormones in endometrial cancer etiology remains inconsistent. The objective of this study was to investigate if circulating levels of endogenous estrone, estradiol, sex hormone binding globulin (SHBG), testosterone, and androstenedione are associated with endometrial cancer risk. Methods We conducted a population-based case–control study of 522 incident endometrial cancer cases and 976 population controls, in Alberta, Canada from 2002 to 2006. Study participants completed in-person interviews and provided fasting blood samples. Sex hormone levels were determined by enzyme-linked immunosorbent assays. Results Higher levels of androstenedione were associated with increased endometrial cancer risk (OR 1.44, 95% CI 1.04–2.02). Endometrial cancer risk in pre- and peri-menopausal women was reduced for the highest versus lowest quartiles of estrone (OR 0.44, 95% CI 0.22–0.88) and estradiol (OR 0.30, 95% CI 0.14–0.65), but in post-menopausal women, the endometrial cancer risk was increased for the highest versus lowest quartile of androstenedione (OR 1.82, 95% CI 1.25–2.65). In addition, endometrial cancer risk in normal/underweight women was decreased for the highest versus lowest quartile of serum SHBG (OR 0.39, 95% CI 0.19–0.84). Conclusions Overall, positive associations were found for androstenedione concentrations, while sub-group analyses revealed = inverse associations with estrogens and SHBG. Results of this study provide empirical evidence for the role of circulating sex hormones in endometrial cancer etiology and highlight the importance of modifiable factors that contribute to changes in sex hormone concentration levels.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>31865473</pmid><doi>10.1007/s10552-019-01260-5</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4783-1966</orcidid></addata></record>
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subjects 17β-Estradiol
Aged
Alberta - epidemiology
Androstenedione
Biomedical and Life Sciences
Biomedicine
Cancer
Cancer Research
Case-Control Studies
Empirical analysis
Endometrial cancer
Endometrial Neoplasms - epidemiology
Endometrium
Epidemiology
Estrogens
Estrone
Etiology
Female
Globulins
Gonadal Steroid Hormones - blood
Health risk assessment
Health risks
Hematology
Hormone replacement therapy
Hormones
Humans
Immunoassays
Menopause
Middle Aged
Oncology
Original Paper
Population studies
Post-menopause
Prospective Studies
Public Health
Quartiles
Risk
Sex Hormone-Binding Globulin - analysis
Sex hormones
Steroid hormones
Steroids
Testosterone
Underweight
title Case–control study of endogenous sex steroid hormones and risk of endometrial cancer
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