# The Rate of Cortisol Decline After Consuming a High-Fat Test Meal for Breakfast Partially Explained Sex-Dependent Variation in Post Ingestive Cardiovascular Status

**Authors:** Kevin D Laugero, Ryan G Snodgrass, Nancy L Keim

PMC · DOI: 10.1016/j.cdnut.2026.107655 · Current Developments in Nutrition · 2026-02-06

## TL;DR

This study found that how quickly cortisol drops after breakfast differs between men and women, which may explain some sex-based differences in cardiovascular responses later in the day.

## Contribution

The study identifies postprandial cortisol decline as a potential mediator of sex-based differences in cardiovascular reactivity.

## Key findings

- Females showed a sharper decline in salivary cortisol after a high-fat meal compared to males.
- Higher postprandial cortisol was linked to increased cardiovascular reactivity during anger induction.
- Postprandial cortisol partially explained sex-based differences in cardiovascular status.

## Abstract

Circulating cortisol concentrations are connected to diet and the neurological systems that regulate food intake. Skipping breakfast can diminish the typical drop in circulating cortisol concentrations.

Determine 1) whether overnight fasted males and females differ in salivary cortisol (CORT) dynamics after consuming a high-fat test meal, 2) if these differences in postprandial (PP) CORT explain variation in cardiovascular status later in the day, and 3) whether PP CORT mediates sex-based differences in cardiovascular status.

This cross-sectional study examined >300 male and female participants. The recruitment sampling scheme consisted of sex (male and female) × age (18‒33 y, 34‒49 y, 50‒65 y) × BMI (normal weight: 18.5‒24.99, overweight: 25‒29.99, and obese: 30‒39.99). The study test visit was conducted at the USDA Western Human Nutrition Research Center and included a high-fat test meal, an emotion-induction (anger recall) task, and collection of blood, saliva, self-reported mood, and physiological information under fasted, PP, and post anger-recall conditions.

After an overnight fast and following the test meal, PP CORT descended significantly (Ptime × sex = 0.00008) more sharply in females compared with males. Fasting CORT did not differ (P = 0.620) between males and females, but females displayed lower CORT at 30 min (P < 0.007), 60 min (P < 0.005), and 90 min (P < 0.010) following the test meal. Higher PP CORT associated with elevated anger-induced heart rate (β: 0.050 ± 0.022; P = 0.0232), elevated anger-induced sympathetic tone (β: 0.232 ± 0.105; P = 0.0282), and lower endothelial function (β: ‒0.1637 ± 0.0698; P = 0.0197). Endothelial function, and anger-induced heart rate and sympathetic tone differed between males and females, with variation in PP CORT partially explaining these sex-based differences.

The magnitude of CORT decline after consuming the first daily meal may contribute to sex-based differences in downstream cardiovascular reactivity.

## Full-text entities

- **Genes:** POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, CRH (corticotropin releasing hormone) [NCBI Gene 1392] {aka CRF, CRH1}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** Cushing's syndrome (MESH:D003480), type 2 diabetes (MESH:D003924), obese (MESH:D009765), overweight (MESH:D050177), hyperemia (MESH:D006940), psychiatric disease (MESH:D001523), cardiovascular disease (MESH:D002318), diabetic (MESH:D003920), insulin resistance (MESH:D007333), Inflammatory (MESH:D007249), arterial occlusion (MESH:D001157)
- **Chemicals:** norepinephrine (MESH:D009638), steroid (MESH:D013256), lipid (MESH:D008055), sucrose (MESH:D013395), glycogen (MESH:D006003), palm oil (MESH:D000073878), CORT (MESH:D006854), EDTA (MESH:D004492), corticosterone (MESH:D003345), carbohydrate (MESH:D002241), SNStone (-), fat (MESH:D005223), metyrapone (MESH:D008797)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966908/full.md

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Source: https://tomesphere.com/paper/PMC12966908