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Menopausal Hormone Therapy and Breast Cancer Risk: Effect Modification by Body Mass Through Life

Overview
Journal Eur J Epidemiol
Specialty Public Health
Date 2018 Aug 8
PMID 30083811
Citations 2
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Abstract

It is not known whether increased breast cancer risk caused by menopausal hormone therapy (HT) depends on body mass patterns through life. In a prospective study of 483,241 Norwegian women aged 50-69 years at baseline, 7656 women developed breast cancer during follow-up (2006-2013). We combined baseline information on recalled body mass in childhood/adolescence and current (baseline) body mass index (BMI) to construct mutually exclusive life-course body mass patterns. We assessed associations of current HT use with breast cancer risk according to baseline BMI and life-course patterns of body mass, and estimated relative excess risk due to interaction (RERI). Within all levels of baseline BMI, HT use was associated with increased risk. Considering life-course body mass patterns as a single exposure, we used women who "remained at normal weight" through life as the reference, and found that being "overweight as young" was associated with lower risk (hazard ratio (HR) 0.85, 95% confidence interval (CI) 0.76-0.94), whereas women who "gained weight" had higher risk (HR 1.20, 95% CI 1.12-1.28). Compared to never users of HT who were "overweight as young", HT users who either "remained at normal weight" or "gained weight" in adulthood were at higher risk than expected when adding the separate risks (RERI 0.52, 95% CI 0.09-0.95, and RERI 0.37, 95% CI - 0.07-0.80), suggesting effect modification. Thus, we found that women who remain at normal weight or gain weight in adulthood may be more susceptible to the risk increasing effect of HT compared to women who were overweight as young.

Citing Articles

Is Breast Cancer Risk Associated with Menopausal Hormone Therapy Modified by Current or Early Adulthood BMI or Age of First Pregnancy?.

Leventea E, Harkness E, Brentnall A, Howell A, Evans D, Harvie M Cancers (Basel). 2021; 13(11).

PMID: 34072619 PMC: 8199436. DOI: 10.3390/cancers13112710.


Objectives, design and main findings until 2020 from the Rotterdam Study.

Ikram M, Brusselle G, Ghanbari M, Goedegebure A, Ikram M, Kavousi M Eur J Epidemiol. 2020; 35(5):483-517.

PMID: 32367290 PMC: 7250962. DOI: 10.1007/s10654-020-00640-5.

References
1.
Chlebowski R, Hendrix S, Langer R, Stefanick M, Gass M, Lane D . Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women: the Women's Health Initiative Randomized Trial. JAMA. 2003; 289(24):3243-53. DOI: 10.1001/jama.289.24.3243. View

2.
Stuenkel C, Davis S, Gompel A, Lumsden M, Murad M, Pinkerton J . Treatment of Symptoms of the Menopause: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2015; 100(11):3975-4011. DOI: 10.1210/jc.2015-2236. View

3.
Moyer V . Medications to decrease the risk for breast cancer in women: recommendations from the U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2013; 159(10):698-708. DOI: 10.7326/0003-4819-159-10-201311190-00717. View

4.
Teraoka H, Tsukada K . Biosynthesis of mammalian DNA ligase. J Biol Chem. 1985; 260(5):2937-40. View

5.
Hou N, Hong S, Wang W, Olopade O, Dignam J, Huo D . Hormone replacement therapy and breast cancer: heterogeneous risks by race, weight, and breast density. J Natl Cancer Inst. 2013; 105(18):1365-72. PMC: 3776262. DOI: 10.1093/jnci/djt207. View