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Circulating inflammatory markers linked to dysregulated postprandial metabolism in postmenopausal women

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Author(s):
Donado-Pestana, Carlos M. ; Vasconcelos, Amanda D. ; Mantovam, Vinicius B. ; de Lima, Gustavo C. ; Rodrigues, Larissa ; Barbeiro, Hermes, V ; Fock, Ricardo ; de Souza, Heraldo P. ; Franco, Bernadette D. G. de M. ; Fiamoncini, Jarlei
Total Authors: 10
Document type: Journal article
Source: JOURNAL OF NUTRITIONAL BIOCHEMISTRY; v. 143, p. 9-pg., 2025-09-01.
Abstract

Menopause induces physiological alterations predisposing women to the development of chronic diseases. The evaluation of postprandial responses allows for a comprehensive assessment of metabolism and biomarkers that may predispose to chronic disease risk. By applying a dietary challenge consisting of the ingestion of a liquid, energy-dense mixed meal, followed by blood sampling over a 6-hour period, we conducted a cross-sectional study to investigate the postprandial metabolism in postmenopausal women (PM) aged 50-70 years and women of reproductive age (RA) aged 20 and 40 years. PM body weight was only 10% higher than RA, but the first displayed twice as much (more than 20%) intrabdominal adipose tissue. PM also displayed elevated fasting and postprandial glycemia (similar to 20%) and lipidemia compared to RA. Differences were also observed in the postprandial levels of lactate. Both groups displayed a similar increase in white blood cell count during the challenge, despite large differences in peripheral blood mononuclear cells (PBMC) gene expression in both fasting and postprandial states, suggesting a pro-inflammatory state and HIF-alpha and glycolytic pathway activation in PM. Plasma levels of monocyte chemoattractant protein-1 (MCP-1) and tumor necrosis factor-alpha (TNF-alpha) were increased in PM (37 and 52%, respectively). Postprandial plasma levels of incretins presented different kinetics to each group. Our findings reveal that PM display a proinflammatory signature and markers of metabolic deterioration after a 12-h fasting and in the postprandial period when compared to RA. (c) 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. (AU)

FAPESP's process: 23/02522-6 - Characterization of the postprandial profile of endocannabinoids in women: Effects of aging
Grantee:Vinicius Bonfieti Mantovam
Support Opportunities: Scholarships in Brazil - Master
FAPESP's process: 21/09237-0 - Postprandial metabolism and inflammation: the role of bile acids as signaling molecules
Grantee:Larissa Rodrigues
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 22/02941-6 - Bile acids as determinants of postprandial metabolism and intestinal microbial colonization in newborns
Grantee:Jarlei Fiamoncini
Support Opportunities: Research Grants - Initial Project
FAPESP's process: 22/08109-0 - Evaluation of the aging effects on postprandial responses: comparison between reproductive-age and postmenopausal women.
Grantee:Amanda Domingos Vasconcelos
Support Opportunities: Scholarships in Brazil - Master
FAPESP's process: 20/16542-0 - Relationship between inflammation and primary metabolism in the postprandial period
Grantee:Carlos Mario Donado Pestana
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 13/07914-8 - FoRC - Food Research Center
Grantee:Bernadette Dora Gombossy de Melo Franco
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC