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DC Field | Value | Language |
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dc.contributor.author | Farhat, Ghada N. | en_US |
dc.contributor.author | Cummings, Steven R. | en_US |
dc.contributor.author | Chlebowski, Rowan T. | en_US |
dc.contributor.author | Parimi, Neeta | en_US |
dc.contributor.author | Cauley, Jane A | en_US |
dc.contributor.author | Rohan, Thomas E. | en_US |
dc.contributor.author | Huang, Alison J. | en_US |
dc.contributor.author | Vitolins, Mara | en_US |
dc.contributor.author | Hubbell, F. Allan | en_US |
dc.date.accessioned | 2020-12-23T09:15:14Z | - |
dc.date.available | 2020-12-23T09:15:14Z | - |
dc.date.issued | 2011 | - |
dc.identifier.uri | https://scholarhub.balamand.edu.lb/handle/uob/2534 | - |
dc.description.abstract | Background Endogenous sex hormone levels are associated with risks of breast cancer overall and estrogen receptor (ER)–positive breast tumors; however, their associations with ER-negative tumors remain unclear. Methods In a case–cohort study within the Womens Health Initiative Observational Study among postmenopausal women aged 50–79 years, we examined associations between endogenous testosterone and estradiol levels and the risks of ER-negative and ER-positive breast cancers. Serum levels of bioavailable testosterone and estradiol were assessed at the baseline visit in 317 invasive breast cancer case subjects and in a subcohort of 594 women. Bioavailable sex hormone levels were calculated using the total hormone level and the sex hormone–binding globulin concentration (measured by radioimmunoassays and a chemiluminescent immunoassay, respectively). Cox proportional hazards regression was used for statistical analysis. All statistical tests were two-sided. Result The unadjusted absolute rates of ER-negative breast cancer for testosterone quartiles 1–4 were 0.34, 0.20, 0.23, and 0.21 per 10 000 person-years, respectively. Compared with women in the lowest quartile of testosterone level, those in quartile 2 had a 56% lower risk of ER-negative cancer (hazard ratio [HR] = 0.44, 95% confidence interval [CI] = 0.23 to 0.85), those in quartile 3 had a 45% lower risk (HR = 0.55, 95% CI = 0.30 to 1.01), and those in quartile 4 had a 49% lower risk (HR = 0.51, 95% CI = 0.28 to 0.94), independent of other risk factors. Estradiol level was not associated with ER-negative breast cancer. ER-positive breast cancer risk increased with higher testosterone levels ( Ptrend = .04), but this trend was not statistically significant after adjustment for estradiol ( Ptrend = .15). ER-positive cancer risk was approximately twofold higher in women with estradiol levels in quartiles 2–4 compared with women in quartile 1, independent of risk factors. Conclusion Higher serum level. | en_US |
dc.format.extent | 9 p. | en_US |
dc.language.iso | eng | en_US |
dc.subject | Testosterone | en_US |
dc.subject | Estradiol | en_US |
dc.subject | Gonadal steroid hormones | en_US |
dc.subject | Testosterone measurement | en_US |
dc.subject | Estrogen receptor negative | en_US |
dc.subject | Breast cancer risk | en_US |
dc.subject.lcsh | Cancer | en_US |
dc.subject.lcsh | Breast cancer | en_US |
dc.title | Sex hormone levels and risks of estrogen receptor-negative and estrogen receptor-positive breast cancers | en_US |
dc.type | Journal Article | en_US |
dc.identifier.doi | 10.1093/jnci/djr031 | - |
dc.contributor.affiliation | Department of Public Health | en_US |
dc.description.volume | 103 | en_US |
dc.description.issue | 7 | en_US |
dc.description.startpage | 562 | en_US |
dc.description.endpage | 570 | en_US |
dc.date.catalogued | 2018-10-23 | - |
dc.description.status | Published | en_US |
dc.identifier.ezproxyURL | http://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1093/jnci/djr031 | en_US |
dc.identifier.OlibID | 186735 | - |
dc.relation.ispartoftext | Journal of the national cancer institute | en_US |
dc.provenance.recordsource | Olib | en_US |
Appears in Collections: | Department of Public Health |
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