TY - JOUR
T1 - Associations of Circulating Estrogens and Estrogen Metabolites with Fecal and Oral Microbiome in Postmenopausal Women in the Ghana Breast Health Study
AU - Wu, Zeni
AU - Pfeiffer, Ruth M.
AU - Byrd, Doratha A.
AU - Wan, Yunhu
AU - Ansong, Daniel
AU - Clegg-Lamptey, Joe Nat
AU - Wiafe-Addai, Beatrice
AU - Edusei, Lawrence
AU - Adjei, Ernest
AU - Titiloye, Nicholas
AU - Dedey, Florence
AU - Aitpillah, Francis
AU - Oppong, Joseph
AU - Vanderpuye, Verna
AU - Osei-Bonsu, Ernest
AU - Dagnall, Casey L.
AU - Jones, Kristine
AU - Hutchinson, Amy
AU - Hicks, Belynda D.
AU - Ahearn, Thomas U.
AU - Knight, Rob
AU - Biritwum, Richard
AU - Yarney, Joel
AU - Wiafe, Seth
AU - Awuah, Baffour
AU - Nyarko, Kofi
AU - Garcia-Closas, Montserrat
AU - Sinha, Rashmi
AU - Figueroa, Jonine D.
AU - Brinton, Louise A.
AU - Trabert, Britton
AU - Vogtmann, Emily
N1 - Publisher Copyright:
© 2023 American Society for Microbiology. All rights reserved.
PY - 2023/8
Y1 - 2023/8
N2 - 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.
AB - 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.
KW - estrogens
KW - fecal microbiome
KW - oral microbiome
KW - postmenopausal African women
UR - http://www.scopus.com/inward/record.url?scp=85168242312&partnerID=8YFLogxK
U2 - 10.1128/spectrum.01572-23
DO - 10.1128/spectrum.01572-23
M3 - Article
C2 - 37341612
AN - SCOPUS:85168242312
SN - 2165-0497
VL - 11
JO - Microbiology spectrum
JF - Microbiology spectrum
IS - 4
ER -