# The brain–bone–gut axis: a microbial bridge underlying multisystem comorbidities

**Authors:** Xingli Xu, Qinghan Ma, Peijie You, Jiong Wu

PMC · DOI: 10.3389/fendo.2026.1755305 · Frontiers in Endocrinology · 2026-02-26

## TL;DR

This paper explores how the brain, bones, and gut interact through a microbial bridge, offering a new way to understand and manage multi-system health issues.

## Contribution

The paper introduces the brain–bone–gut axis as a novel integrative framework for understanding multisystem comorbidities.

## Key findings

- The brain–bone–gut axis links the central nervous system, bone metabolism, and gut microbiota through neural, endocrine, and immune pathways.
- Immune-inflammatory processes serve as a central hub connecting gut dysbiosis with bone and brain dysfunction.
- Combining microecological interventions with nutrition and exercise can improve gut, bone, and brain health.

## Abstract

Multi-axis interactions among the skeletal system, immune system, and gut microbiota (GM) have become a prominent focus of interdisciplinary research. The brain–bone–gut axis, proposed in recent years, provides an integrative physiological framework describing a bidirectional regulatory network linking the central nervous system, bone metabolism, and the GM via neural, endocrine, and immune pathways, thereby offering a unified perspective on multi-organ comorbidities. This article systematically examines the interconnections and synergistic effects across three core pathways within this framework: the brain–bone axis, the gut–bone axis, and the gut–brain axis. It further emphasizes immune-inflammatory processes as a central hub that connects gut dysbiosis with bone metabolic disturbances and alterations in brain function. On this basis, we propose an integrated approach that combines microecological interventions with nutritional and exercise management to improve gut homeostasis, preserve skeletal health, and support brain function, with the overarching aim of generating coordinated benefits across organ systems.

## Full-text entities

- **Diseases:** dysbiosis (MESH:D064806), disturbances (MESH:D014832), inflammatory (MESH:D007249)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12979103/full.md

## References

122 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979103/full.md

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Source: https://tomesphere.com/paper/PMC12979103