TY - JOUR
T1 - Baseline estrogen levels in postmenopausal women participating in the MAP.3 breast cancer chemoprevention trial
AU - Richardson, Harriet
AU - Ho, Vikki
AU - Pasquet, Romain
AU - Singh, Ravinder J.
AU - Goetz, Matthew P.
AU - Tu, Dongsheng
AU - Goss, Paul E.
AU - Ingle, James N.
N1 - Funding Information:
Received January 12, 2020; revised and accepted March 20, 2020. From the 1Department of Public Health Sciences and Canadian Cancer Trials Group, Queen’s University, Kingston, Ontario, Canada; 2Centre de Recherche du CHUM (CRCHUM), Montréal, Québec, Canada; 3Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN; 4Division of Medical Oncology, Mayo Clinic, Rochester, MN; and 5Harvard Medical School, MGH Cancer Centre, Boston, MA. Presented, in part, at The North American Menopause Society Workshop on Normal Ranges for Estradiol in Postmenopausal Women, Chicago, IL, September 23, 2019. Funding/support: This study was supported in part by NIH (NCI) grants P50CA116201 (Mayo Clinic Breast Cancer Specialized Program of Research Excellence) and QUE-182363 (Subaward to Queen’s University). Financial disclosure/conflicts of interest: None reported. Address correspondence to: Harriet Richardson, PhD, Queen’s Cancer Research Institute, Canadian Cancer Trials Group, 10 Stuart St, Kingston, Ontario, Canada K7L3N6. E-mail: hrichardson@ctg.queensu.ca
Publisher Copyright:
© 2020 Lippincott Williams and Wilkins. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Objective:The aim of the study was to quantify baseline estradiol (E2) and estrone (E1) concentrations according to selected patient characteristics in a substudy nested within the MAP.3 chemoprevention trial.Methods:E2 and E1 levels were measured in 4,068 postmenopausal women using liquid chromatography-tandem mass spectrometry. Distributions were described by age, years since menopause, race, body mass index (BMI), smoking status, and use and duration of hormone therapy using the Kruskal-Wallis test. Multivariable linear regression was also used to identify characteristics associated with estrogen levels.Results:After truncation at the 97.5th percentile, the mean (SD)/median (IQR) values for E2 and E1 were 5.41 (4.67)/4.0 (2.4-6.7) pg/mL and 24.7 (14.1)/21 (15-31) pg/mL, respectively. E2 and E1 were strongly correlated (Pearson correlation [r] = 0.8, P < 0.01). The largest variation in E2 and E1 levels was by BMI; mean E2 and E1 levels were 3.5 and 19.1 pg/mL, respectively for women with BMI less than 25 and 7.5 and 30.6 pg/mL, respectively, for women with BMI greater than 30. E2 and E1 varied by age, BMI, smoking status, and prior hormone therapy in multivariable models (P < 0.01).Conclusions:There was large interindividual variability observed for E2 and E1 that varied significantly by participant characteristics, but with small absolute differences except in the case of BMI. Although the majority of participant characteristics were independently associated with E1 and E2, together, these factors only explained about 20% of the variation in E1 and E2 levels.
AB - Objective:The aim of the study was to quantify baseline estradiol (E2) and estrone (E1) concentrations according to selected patient characteristics in a substudy nested within the MAP.3 chemoprevention trial.Methods:E2 and E1 levels were measured in 4,068 postmenopausal women using liquid chromatography-tandem mass spectrometry. Distributions were described by age, years since menopause, race, body mass index (BMI), smoking status, and use and duration of hormone therapy using the Kruskal-Wallis test. Multivariable linear regression was also used to identify characteristics associated with estrogen levels.Results:After truncation at the 97.5th percentile, the mean (SD)/median (IQR) values for E2 and E1 were 5.41 (4.67)/4.0 (2.4-6.7) pg/mL and 24.7 (14.1)/21 (15-31) pg/mL, respectively. E2 and E1 were strongly correlated (Pearson correlation [r] = 0.8, P < 0.01). The largest variation in E2 and E1 levels was by BMI; mean E2 and E1 levels were 3.5 and 19.1 pg/mL, respectively for women with BMI less than 25 and 7.5 and 30.6 pg/mL, respectively, for women with BMI greater than 30. E2 and E1 varied by age, BMI, smoking status, and prior hormone therapy in multivariable models (P < 0.01).Conclusions:There was large interindividual variability observed for E2 and E1 that varied significantly by participant characteristics, but with small absolute differences except in the case of BMI. Although the majority of participant characteristics were independently associated with E1 and E2, together, these factors only explained about 20% of the variation in E1 and E2 levels.
KW - Estradiol
KW - Estrone
KW - Postmenopausal women
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U2 - 10.1097/GME.0000000000001568
DO - 10.1097/GME.0000000000001568
M3 - Article
C2 - 32433262
AN - SCOPUS:85085586245
SN - 1072-3714
VL - 27
SP - 693
EP - 700
JO - Menopause
JF - Menopause
IS - 6
ER -