Affiliation:
1. Shenzhen Guangming District People’s Hospital, Shenzhen, China
2. First Affiliated Hospital, Heilongjiang University of Chinese Medicine, Harbin, China
3. Chemical Analysis and Physical Testing Institute, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
Abstract
Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural deterioration, resulting in increased fracture risk. With an aging population, osteoporosis imposes a heavy burden worldwide. Current pharmacotherapies such as bisphosphonates can reduce fracture risk but have limitations. Emerging research suggests that gut microbiota regulates bone metabolism through multiple mechanisms. Short-chain fatty acids (SCFAs) produced from microbial fermentation of dietary fiber beneficially impact bone health. Preclinical studies indicate that SCFAs such as butyrate and propionate prevent bone loss in osteoporosis models by inhibiting osteoclastogenesis and immune modulation. Early clinical data also suggest that SCFA supplementation may improve bone turnover markers in postmenopausal women. SCFAs likely act via inhibition of osteoclast differentiation, stimulation of osteoblast activity, regulation of T cells, and other pathways. However, optimal dosing, delivery methods, and long-term safety require further investigation. Modulating the gut-bone axis via supplementation, prebiotics/probiotics, diet, and lifestyle interventions represents an innovative therapeutic approach for osteoporosis. Harnessing the interplay between microbiome, metabolism, immunity, and bone may provide new directions for managing osteoporosis in the future.
Funder
Guangdong Basic and Applied Basic Research Foundation
Shenzhen Science and Technology Program
Shenzhen Postdoctoral Research Fund for Staying in Shenzhen
Publisher
Ovid Technologies (Wolters Kluwer Health)