Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Feb;36(2):167-191.
doi: 10.1007/s00198-024-07320-0. Epub 2024 Dec 7.

Gut microbiome and bone health: update on mechanisms, clinical correlations, and possible treatment strategies

Affiliations

Gut microbiome and bone health: update on mechanisms, clinical correlations, and possible treatment strategies

Andrea Ticinesi et al. Osteoporos Int. 2025 Feb.

Abstract

The intestinal microbiome is increasingly regarded as a relevant modulator of the pathophysiology of several age-related conditions, including frailty, sarcopenia, and cognitive decline. Aging is in fact associated with alteration of the equilibrium between symbiotic bacteria and opportunistic pathogens, leading to dysbiosis. The microbiome is able to regulate intestinal permeability and systemic inflammation, has a central role in intestinal amino acid metabolism, and produces a large number of metabolites and byproducts, with either beneficial or detrimental consequences for the host physiology. Recent evidence, from both preclinical animal models and clinical studies, suggests that these microbiome-centered pathways could contribute to bone homeostasis, regulating the balance between osteoblast and osteoclast function. In this systematic review, we provide an overview of the mechanisms involved in the gut-bone axis, with a particular focus on microbiome function and microbiome-derived mediators including short-chain fatty acids. We also review the current evidence linking gut microbiota dysbiosis with osteopenia and osteoporosis, and the results of the intervention studies on pre-, pro-, or post-biotics targeting bone mineral density loss in both animal models and human beings, indicating knowledge gaps and highlighting possible avenues for future research.

Keywords: Dysbiosis; Gut–bone axis; Osteoblast; Osteoclast; Probiotic; SCFA.

PubMed Disclaimer

Conflict of interest statement

Declarations. Conflict of interest: The authors declare no competing interests.

References

    1. Fan Y, Pedersen O (2021) Gut microbiota in human metabolic health and disease. Nat Rev Microbiol 19(1):55–71 - PubMed
    1. Gacesa R, Kurilshikov A, Vich Vila A et al (2022) Environmental factors shaping the gut microbiome in a Dutch population. Nature 604(7907):732–739 - PubMed
    1. Mancabelli L, Milani C, De Biase R et al (2024) Taxonomic and metabolic development of the human gut microbiome across life stages: a worldwide metagenomic investigation. mSystems 9((4)):e0129423 - PubMed
    1. Kurilshikov A, Medina-Gomez C, Bacigalupe R et al (2021) Large-scale association analyses identify host factors influencing human gut microbiome composition. Nat Genet 53(2):156–165 - PubMed - PMC
    1. Geuking MB, Köller Y, Rupp S, McCoy KD (2014) The interplay between the gut microbiota and the immune system. Gut Microbes 5(3):411–418 - PubMed - PMC

Publication types

LinkOut - more resources