Department of Biomedical Engineering, University of Massachusetts Amherst, Amherst, MA, United States.
Institute for Applied Life Sciences, University of Massachusetts Amherst, Amherst, MA, United States.
Front Endocrinol (Lausanne). 2023 Oct 9;14:1229796. doi: 10.3389/fendo.2023.1229796. eCollection 2023.
The gut microbiome has been implicated in a multitude of human diseases, with emerging evidence linking its microbial diversity to osteoporosis. This review article will explore the molecular mechanisms underlying perturbations in the gut microbiome and their influence on osteoporosis incidence in individuals with chronic diseases. The relationship between gut microbiome diversity and bone density is primarily mediated by microbiome-derived metabolites and signaling molecules. Perturbations in the gut microbiome, induced by chronic diseases can alter bacterial diversity and metabolic profiles, leading to changes in gut permeability and systemic release of metabolites. This cascade of events impacts bone mineralization and consequently bone mineral density through immune cell activation. In addition, we will discuss how orally administered medications, including antimicrobial and non-antimicrobial drugs, can exacerbate or, in some cases, treat osteoporosis. Specifically, we will review the mechanisms by which non-antimicrobial drugs disrupt the gut microbiome's diversity, physiology, and signaling, and how these events influence bone density and osteoporosis incidence. This review aims to provide a comprehensive understanding of the complex interplay between orally administered drugs, the gut microbiome, and osteoporosis, offering new insights into potential therapeutic strategies for preserving bone health.
肠道微生物群与多种人类疾病有关,越来越多的证据表明其微生物多样性与骨质疏松症有关。这篇综述文章将探讨肠道微生物群失调的分子机制及其对慢性病患者骨质疏松症发病率的影响。肠道微生物多样性与骨密度之间的关系主要由微生物衍生的代谢物和信号分子介导。慢性病引起的肠道微生物群失调会改变细菌多样性和代谢谱,导致肠道通透性改变和代谢物全身性释放。这一连串事件通过免疫细胞激活影响骨矿化,进而影响骨密度。此外,我们还将讨论口服药物(包括抗菌和非抗菌药物)如何加重或在某些情况下治疗骨质疏松症。具体来说,我们将回顾非抗菌药物破坏肠道微生物群多样性、生理学和信号转导的机制,以及这些事件如何影响骨密度和骨质疏松症发病率。本综述旨在全面了解口服药物、肠道微生物群和骨质疏松症之间的复杂相互作用,为保护骨骼健康提供新的治疗策略。