Association of ß-glucuronidase activity with menopausal status, ethnicity, adiposity, and inflammation in women.


Journal

Menopause (New York, N.Y.)
ISSN: 1530-0374
Titre abrégé: Menopause
Pays: United States
ID NLM: 9433353

Informations de publication

Date de publication:
01 02 2023
Historique:
pmc-release: 20 11 2024
entrez: 25 1 2023
pubmed: 26 1 2023
medline: 28 1 2023
Statut: ppublish

Résumé

Many dietary polyphenols with potential health-promoting benefits undergo hepatic conjugation and circulate as inactive glucuronides that can be cleaved by ß-glucuronidase to reform the bioactive aglycone. Although indirect evidence suggests estrogen may induce ß-glucuronidase, little is known about ß-glucuronidase regulation across women's reproductive lifespan. Correlates of serum ß-glucuronidase activity in healthy premenopausal versus postmenopausal women were therefore examined. ß-Glucuronidase activity and C-reactive protein (CRP) were assayed in stored serum from the Women's Breast and Bone Density Study, and dual-energy x-ray absorptiometry and anthropometry assessed body composition. Participants were premenopausal (n = 133) or postmenopausal (n = 89), and Hispanic (37%) or non-Hispanic White (63%). Multivariate linear regression models tested associations between ß-glucuronidase and menopausal status, ethnicity, CRP, and body composition metrics, overall and stratified by menopausal status. Postmenopausal (vs premenopausal) women were older (60.4 ± 3.7 vs 44.8 ± 2.4 y) with a lower Hispanic ethnicity prevalence (27% vs 44%), and higher serum ß-glucuronidase activity (1.5 ± 0.8 vs 1.3 ± 0.5 U/L) and CRP (4.2 ± 4.4 vs 3.3 ± 4.7 mg/L). Adjusting for confounders, ß-glucuronidase was positively associated with Hispanic ethnicity, CRP, body mass index, and total fat mass (all, P < 0.01), but not menopausal status nor lean mass. Central adiposity measures were also positively associated with ß-glucuronidase with the same covariates. ß-Glucuronidase enzyme activity, upon which polyphenol health-related benefits may depend, is not associated with menopausal status. Future studies are required to determine clinical significance and mechanisms driving ß-glucuronidase associations with ethnicity, inflammation, and adiposity in women.

Identifiants

pubmed: 36696643
doi: 10.1097/GME.0000000000002106
pii: 00042192-202302000-00012
pmc: PMC9886315
mid: NIHMS1836621
doi:

Substances chimiques

C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

186-192

Subventions

Organisme : NCI NIH HHS
ID : P30 CA023074
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA174926
Pays : United States
Organisme : NIAMS NIH HHS
ID : R21 AR078424
Pays : United States
Organisme : NCI NIH HHS
ID : R25 CA217725
Pays : United States

Informations de copyright

Copyright © 2022 by The North American Menopause Society.

Déclaration de conflit d'intérêts

Financial disclosure/conflicts of interest: J.L.F. received a past research grant from Metavivor Foundation. J.W.B. received grant funding from Disarm Therapeutics to her institution for an unrelated IIT to study biomarkers of chemotherapy-induced peripheral neuropathy. She is also a board member of Global Health and Body Composition Institute. The other authors have nothing to disclose.

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Auteurs

Betsy C Wertheim (BC)

University of Arizona Cancer Center, University of Arizona, Tucson, AZ.

Jennifer B Frye (JB)

From the Department of Medicine, College of Medicine, University of Arizona, Tucson, AZ.

Jennifer Skye Nicholas (JS)

Department of Epidemiology and Biostatistics Department, Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, AZ.

Zhao Chen (Z)

Department of Epidemiology and Biostatistics Department, Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, AZ.

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