Shenzhen Guangming District People's Hospital, Shenzhen, China.
First Affiliated Hospital, Heilongjiang University of Chinese Medicine, Harbin, China.
Medicine (Baltimore). 2024 Aug 23;103(34):e39471. doi: 10.1097/MD.0000000000039471.
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.
骨质疏松症是一种全身性骨骼疾病,其特征是骨密度低和微结构恶化,导致骨折风险增加。随着人口老龄化,骨质疏松症在全球造成了沉重负担。目前的药物治疗方法,如双磷酸盐类药物,可以降低骨折风险,但存在局限性。新的研究表明,肠道微生物群通过多种机制调节骨骼代谢。膳食纤维经微生物发酵产生的短链脂肪酸(SCFAs)对骨骼健康有益。临床前研究表明,丁酸盐和丙酸盐等 SCFAs 通过抑制破骨细胞生成和免疫调节来预防骨质疏松症模型中的骨质流失。早期临床数据还表明,SCFA 补充剂可能改善绝经后妇女的骨转换标志物。SCFAs 可能通过抑制破骨细胞分化、刺激成骨细胞活性、调节 T 细胞和其他途径发挥作用。然而,最佳剂量、给药方法和长期安全性仍需要进一步研究。通过补充、益生元/益生菌、饮食和生活方式干预来调节肠道-骨骼轴,为骨质疏松症提供了一种创新的治疗方法。利用微生物组、代谢、免疫和骨骼之间的相互作用,可能为未来管理骨质疏松症提供新的方向。