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Important Role of Menarche in Development of Estrogen Receptor-Negative Breast Cancer in African American Women.

Authors :
Ambrosone CB
Zirpoli G
Hong CC
Yao S
Troester MA
Bandera EV
Schedin P
Bethea TN
Borges V
Park SY
Chandra D
Rosenberg L
Kolonel LN
Olshan AF
Palmer JR
Source :
Journal of the National Cancer Institute [J Natl Cancer Inst] 2015 Jun 17; Vol. 107 (9). Date of Electronic Publication: 2015 Jun 17 (Print Publication: 2015).
Publication Year :
2015

Abstract

Background: Menarche is a critical time point for diverging fates of mammary cells of origin. African American women have young age at menarche, which could be associated with their high rates of estrogen receptor-negative (ER-) breast cancer.<br />Methods: In the AMBER Consortium, using harmonized data from 4426 African American women with breast cancer and 17 474 controls, we used polytomous logistic regression to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for ages at menarche and first live birth (FLB), and the interval between, in relation to ER+ and ER- breast cancer. All statistical tests were two-sided.<br />Results: Risk of ER- breast cancer was reduced with later age at menarche among both parous and nulliparous women (≥15 vs <11 years OR = 0.62, 95% CI = 0.48 to 0.81 and OR = 0.56, 95% CI = 0.29 to 1.10, respectively), with no effect of age at FLB. For ER+ breast cancer, the inverse association was weaker among nulliparous women. While longer intervals between menarche and FLB were associated with increased risk of ER+ breast cancer in a dose-response fashion (OR for 20 year interval = 1.39, 95% CI = 1.08 to 1.79, P trend = .003), ER- risk was only increased for intervals up to 14 years and not beyond (P trend = .33).<br />Conclusions: While ER- breast cancer risk was markedly reduced in women with a late age at menarche, there was not a clear pattern of increased risk with longer interval between menarche and FLB, as was observed for ER+ breast cancer. These findings indicate that etiologic pathways involving adolescence and pregnancy may differ for ER- and ER+ breast cancer.<br /> (© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1460-2105
Volume :
107
Issue :
9
Database :
MEDLINE
Journal :
Journal of the National Cancer Institute
Publication Type :
Academic Journal
Accession number :
26085483
Full Text :
https://doi.org/10.1093/jnci/djv172