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Associations of Circulating Estrogens and Estrogen Metabolites with Fecal and Oral Microbiome in Postmenopausal Women in the Ghana Breast Health Study

  • Zeni Wu
  • , Ruth M. Pfeiffer
  • , Doratha A. Byrd
  • , Yunhu Wan
  • , Daniel Ansong
  • , Joe Nat Clegg-Lamptey
  • , Beatrice Wiafe-Addai
  • , Lawrence Edusei
  • , Ernest Adjei
  • , Nicholas Titiloye
  • , Florence Dedey
  • , Francis Aitpillah
  • , Joseph Oppong
  • , Verna Vanderpuye
  • , Ernest Osei-Bonsu
  • , Casey L. Dagnall
  • , Kristine Jones
  • , Amy Hutchinson
  • , Belynda D. Hicks
  • , Thomas U. Ahearn
  • Rob Knight, Richard Biritwum, Joel Yarney, Seth Wiafe, Baffour Awuah, Kofi Nyarko, Montserrat Garcia-Closas, Rashmi Sinha, Jonine D. Figueroa, Louise A. Brinton, Britton Trabert, Emily Vogtmann
  • National Institutes of Health
  • Moffitt Cancer Center
  • Komfo Anokye Teaching Hospital
  • Korle Bu Teaching Hospital
  • Peace and Love Hospital
  • US Department of Health and Human Services
  • University of California at San Diego
  • University of Ghana
  • Loma Linda University Health
  • University of Edinburgh
  • University of Utah School of Medicine

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Abstract

The human fecal and oral microbiome may play a role in the etiology of breast cancer through modulation of endogenous estrogen metabolism. This study aimed to investigate associations of circulating estrogens and estrogen metabolites with the fecal and oral microbiome in postmenopausal African women. A total of 117 women with fecal (N = 110) and oral (N = 114) microbiome data measured by 16S rRNA gene sequencing, and estrogens and estrogen metabolites data measured by liquid chromatography tandem mass spectrometry were included. The outcomes were measures of the microbiome and the independent variables were the estrogens and estrogen metabolites. Estrogens and estrogen metabolites were associated with the fecal microbial Shannon index (global P < 0.01). In particular, higher levels of estrone (b = 0.36, P = 0.03), 2-hydroxyestradiol (b = 0.30, P = 0.02), 4-methoxyestrone (b = 0.51, P = 0.01), and estriol (b = 0.36, P = 0.04) were associated with higher levels of the Shannon index, while 16alpha-hydroxyestrone (b = 20.57, P , 0.01) was inversely associated with the Shannon index as indicated by linear regression. Conjugated 2-methoxyestrone was associated with oral microbial unweighted UniFrac as indicated by MiRKAT (P < 0.01) and PERMANOVA, where conjugated 2-methoxyestrone explained 2.67% of the oral microbial variability, but no other estrogens or estrogen metabolites were associated with any other beta diversity measures. The presence and abundance of multiple fecal and oral genera, such as fecal genera from families Lachnospiraceae and Ruminococcaceae, were associated with several estrogens and estrogen metabolites as indicated by zero-inflated negative binomial regression. Overall, we found several associations of specific estrogens and estrogen metabolites and the fecal and oral microbiome.

Original languageEnglish
JournalMicrobiology spectrum
Volume11
Issue number4
DOIs
Publication statusPublished - Aug 2023
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • estrogens
  • fecal microbiome
  • oral microbiome
  • postmenopausal African women

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