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Untargeted serum metabolomic profiles and breast density in young women.

Authors
  • Jung, Seungyoun1, 2
  • Silva, Sarah3
  • Dallal, Cher M4
  • LeBlanc, Erin5
  • Paris, Kenneth6
  • Shepherd, John7
  • Snetselaar, Linda G8
  • Van Horn, Linda9
  • Zhang, Yuji10
  • Dorgan, Joanne F11
  • 1 Department of Nutritional Science and Food Management, Ewha Womans University, Seoul, South Korea. , (North Korea)
  • 2 Graduate Program in System Health Science and Engineering, Ewha Womans University, Seoul, South Korea. , (North Korea)
  • 3 University of Maryland School of Medicine, Baltimore, MD, USA.
  • 4 Department of Epidemiology and Biostatistics, School of Public Health, University of Maryland, College Park, MD, USA.
  • 5 Kaiser Permanente Center for Health Research, Portland, OR, USA.
  • 6 Department of Pediatrics, Louisiana State University School of Medicine, New Orleans, LA, USA.
  • 7 University of Hawaii Cancer Center, Honolulu, HI, USA.
  • 8 Department of Epidemiology, University of Iowa, Iowa City, IA, USA.
  • 9 Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • 10 Division of Cancer Epidemiology, Department of Epidemiology and Public Health, University of Maryland School of Medicine, 660 West Redwood St., Howard Hall, Room 102E, Baltimore, MD, 21201, USA.
  • 11 Division of Cancer Epidemiology, Department of Epidemiology and Public Health, University of Maryland School of Medicine, 660 West Redwood St., Howard Hall, Room 102E, Baltimore, MD, 21201, USA. [email protected].
Type
Published Article
Journal
Cancer Causes & Control
Publisher
Springer-Verlag
Publication Date
Feb 01, 2024
Volume
35
Issue
2
Pages
323–334
Identifiers
DOI: 10.1007/s10552-023-01793-w
PMID: 37737303
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Breast density is an established risk factor for breast cancer. However, little is known about metabolic influences on breast density phenotypes. We conducted untargeted serum metabolomics analyses to identify metabolic signatures associated with breast density phenotypes among young women. In a cross-sectional study of 173 young women aged 25-29 who participated in the Dietary Intervention Study in Children 2006 Follow-up Study, 449 metabolites were measured in fasting serum samples using ultra-high-performance liquid chromatography-tandem mass spectrometry. Multivariable-adjusted mixed-effects linear regression identified metabolites associated with magnetic resonance imaging measured breast density phenotypes: percent dense breast volume (%DBV), absolute dense breast volume (ADBV), and absolute non-dense breast volume (ANDBV). Metabolite results were corrected for multiple comparisons using a false discovery rate adjusted p-value (q). The amino acids valine and leucine were significantly inversely associated with %DBV. For each 1 SD increase in valine and leucine, %DBV decreased by 20.9% (q = 0.02) and 18.4% (q = 0.04), respectively. ANDBV was significantly positively associated with 16 lipid and one amino acid metabolites, whereas no metabolites were associated with ADBV. Metabolite set enrichment analysis also revealed associations of distinct metabolic signatures with %DBV, ADBV, and ANDBV; branched chain amino acids had the strongest inverse association with %DBV (p = 0.002); whereas, diacylglycerols and phospholipids were positively associated with ANDBV (p ≤ 0.002), no significant associations were observed for ADBV. Our results suggest an inverse association of branched chain amino acids with %DBV. Larger studies in diverse populations are needed. © 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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