# Differential Gastric Motility, Gut Hormone, and Appetite Changes Following A Mixed Meal in People With Obesity and Healthy Controls

**Authors:** Darius Javidi, Dominic‐Luc Webb, Hetzel Olenia Diaz, Moeen Ud‐din, Khalid Elias, Magnus Sundbom, Per M. Hellström

PMC · DOI: 10.1111/nmo.70163 · Neurogastroenterology and Motility · 2025-09-17

## TL;DR

This study compares how gut hormones and stomach movement differ after eating in people with obesity and healthy individuals, revealing altered responses in those with obesity.

## Contribution

The study identifies distinct gastric motility and hormone responses in obesity compared to healthy controls after a meal.

## Key findings

- People with obesity showed faster gastric emptying than healthy individuals.
- In healthy individuals, gastric motility correlated with ghrelin and motilin but not in those with obesity.
- GIP and GLP-1 were linked to satiety in both groups, but hormone-motility relationships were disrupted in obesity.

## Abstract

Understanding meal‐induced changes of gut hormones, gastric motility, and appetite is crucial for developing therapies for obesity. We investigated glucose‐dependent insulinotropic peptide (GIP), glucagon‐like peptide‐1 (GLP‐1), ghrelin, and motilin influences on gastric motility and appetite, to compare healthy individuals and people with obesity.

Subjects (healthy n = 41; obesity n = 32) consumed a 270‐kcal meal and a wireless motility capsule. GIP, active GLP‐1, acyl‐ghrelin, and motilin were measured by electrochemiluminescence. MotiliGI and GIMS software were used for motility analysis, while visual analog scoring measured appetite.

Gastric emptying was more rapid in people with obesity than in healthy individuals (p < 0.01). Gastric emptying time was negatively associated with motility index and hunger contractions (p < 0.01, p < 0.05) in healthy individuals, but not in individuals with obesity. In controls, gastric motility index correlated positively with acyl‐ghrelin (p < 0.01) and motilin (p < 0.0001), and negatively with GIP (p < 0.05), but not aGLP‐1. In people with obesity, no gut hormones correlated with the motility index. In both groups, GIP and aGLP‐1 correlated with decreased hunger (p < 0.0001, p = 0.001) and (p < 0.0001, p < 0.05), along with increased satiety in controls (p < 0.0001, p = 0.001) and people with obesity (p = 0.049, p = 0.01). Acyl‐ghrelin correlated positively with hunger (p < 0.0001) and negatively with satiety (p = 0.049) in controls, but not in obesity. Motilin was neither associated with hunger nor satiety.

In the gastric phase, people with obesity show rapid gastric emptying with altered hormone and motility meal responses. In healthy individuals, GIP promotes satiety, and ghrelin and motilin promote hunger through actions on motility. Like GIP, GLP‐1 promotes satiety along with trending suppression of gastric motility.

During the gastric emptying phase after food intake, people with obesity show rapid gastric emptying as compared to healthy subjects. They also display low gut hormone excursions and flatline gastric motility responses. In subjects with obesity, the relationships between gastric motility, GIP, and GLP‐1 versus hunger and satiety were preserved, but disrupted for gastric stimulation by ghrelin and motilin.

## Linked entities

- **Proteins:** GIP (gastric inhibitory polypeptide), GCG (glucagon), GHRL (ghrelin and obestatin prepropeptide), mlnl (motilin-like)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], MLN (motilin) [NCBI Gene 4295]
- **Diseases:** Obesity (MESH:D009765)
- **Chemicals:** Gut Hormone (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12534588/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12534588/full.md

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Source: https://tomesphere.com/paper/PMC12534588