Relationship of Serum Progesterone and Progesterone Metabolites with Mammographic Breast Density and Terminal Ductal Lobular Unit Involution among Women Undergoing Diagnostic Breast Biopsy.

breast cancer breast density liquid chromatography-tandem mass spectrometry mammographic density progesterone serum progesterone assay

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
17 Jan 2020
Historique:
received: 14 11 2019
revised: 06 01 2020
accepted: 09 01 2020
entrez: 23 1 2020
pubmed: 23 1 2020
medline: 23 1 2020
Statut: epublish

Résumé

The association of progesterone/progesterone metabolites with elevated mammographic breast density (MBD) and delayed age-related terminal duct lobular unit (TDLU) involution, strong breast cancer risk factors, has received limited attention. Using a reliable liquid chromatography-tandem mass-spectrometry assay, we quantified serum progesterone/progesterone metabolites and explored cross-sectional relationships with MBD and TDLU involution among women, ages 40-65, undergoing diagnostic breast biopsy. Quantitative MBD measures were estimated in pre-biopsy digital mammograms. TDLU involution was quantified in diagnostic biopsies. Adjusted partial correlations and trends across MBD/TDLU categories were calculated. Pregnenolone was positively associated with percent MBD-area (MBD-A, rho: 0.30; p-trend = 0.01) among premenopausal luteal phase women. Progesterone tended to be positively associated with percent MBD-A among luteal phase (rho: 0.26; p-trend = 0.07) and postmenopausal (rho: 0.17; p-trend = 0.04) women. Consistent with experimental data, implicating an elevated 5α-pregnanes/3α-dihydroprogesterone (5αP/3αHP) metabolite ratio in breast cancer, higher 5αP/3αHP was associated with elevated percent MBD-A among luteal phase (rho: 0.29; p-trend = 0.08), but not postmenopausal women. This exploratory analysis provided some evidence that endogenous progesterone and progesterone metabolites might be correlated with MBD, a strong breast cancer risk factor, in both pre- and postmenopausal women undergoing breast biopsy. Additional studies are needed to understand the role of progesterone/progesterone metabolites in breast tissue composition and breast cancer risk.

Identifiants

pubmed: 31963437
pii: jcm9010245
doi: 10.3390/jcm9010245
pmc: PMC7019918
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Manila Hada (M)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Hannah Oh (H)

Division of Health Policy and Management, College of Health Science, Korea University, Seoul 02841, Korea.

Shaoqi Fan (S)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Roni T Falk (RT)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Berta Geller (B)

Department of Family Medicine, University of Vermont and Vermont Cancer Center, Burlington, VT 05401, USA.

Pamela Vacek (P)

Department of Medical Biostatistics, University of Vermont and Vermont Cancer Center, Burlington, VT 05401, USA.

Donald Weaver (D)

Department of Pathology, University of Vermont and Vermont Cancer Center, Burlington, VT 05401, USA.

John Shepherd (J)

Population Sciences in the Pacific Program (Cancer Epidemiology), University of Hawaii Cancer Center, Honolulu, HI 96813, USA.

Jeff Wang (J)

Graduate School of Medicine, Hokkaido University, Sapporo 060-080, Japan.

Bo Fan (B)

Department of Radiology & Biomedical Imaging, University of California, San Francisco, CA 94115, USA.

Sally Herschorn (S)

Department of Radiology, University of Vermont and Vermont Cancer Center, Burlington, VT 05401, USA.

Louise A Brinton (LA)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Xia Xu (X)

Frederick National Laboratory for Cancer Research, Frederick, MD 21701, USA.

Mark E Sherman (ME)

Mayo Clinic, Jacksonville, FL 32224, USA.

Britton Trabert (B)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Gretchen L Gierach (GL)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Classifications MeSH