Department of Orthopedics, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Orthopedics, Luodian Hospital, Baoshan District, Shanghai, China.
PeerJ. 2024 May 31;12:e17416. doi: 10.7717/peerj.17416. eCollection 2024.
The importance of the gut microbiota in maintaining bone homeostasis has been increasingly emphasized by recent research. This study aimed to identify whether and how the gut microbiome of postmenopausal women with osteoporosis and osteopenia may differ from that of healthy individuals.
Fecal samples were collected from 27 individuals with osteoporosis (OP), 44 individuals with osteopenia (ON), and 23 normal controls (NC). The composition of the gut microbial community was analyzed by 16S rRNA gene sequencing.
No significant difference was found in the microbial composition between the three groups according to alpha and beta diversity. At the phylum level, and were significantly higher and was significantly lower in the ON group than in the NC group. At the genus level, ter and differed between the OP and NC groups as well as between the ON and NC groups ( < 0.05). Linear discriminant effect size (LEfSe) analysis results showed that one phylum community and eighteen genus communities were enriched in the NC, ON and OP groups, respectively. Spearman correlation analysis showed that the abundance of the genus was positively correlated with BMD and T score at the lumbar spine ( < 0.05). Functional predictions revealed that pathways relevant to amino acid biosynthesis, vitamin biosynthesis, and nucleotide metabolism were enriched in the NC group. On the other hand, pathways relevant to metabolites degradation and carbohydrate metabolism were mainly enriched in the ON and OP groups respectively.
Our findings provide new epidemiologic evidence regarding the relationship between the gut microbiota and postmenopausal bone loss, laying a foundation for further exploration of therapeutic targets for the prevention and treatment of postmenopausal osteoporosis (PMO).
最近的研究越来越强调肠道微生物群在维持骨稳态中的重要性。本研究旨在确定绝经后骨质疏松症和骨量减少患者的肠道微生物群是否以及如何与健康个体的肠道微生物群不同。
收集了 27 名骨质疏松症(OP)患者、44 名骨量减少(ON)患者和 23 名正常对照者(NC)的粪便样本。通过 16S rRNA 基因测序分析肠道微生物群落的组成。
根据 alpha 和 beta 多样性,三组之间的微生物组成没有显著差异。在门水平上,ON 组的 和 显著高于 NC 组, 显著低于 NC 组。在属水平上,OP 组和 NC 组以及 ON 组和 NC 组之间的 ter 和 不同(<0.05)。线性判别效应量(LEfSe)分析结果表明,一个门社区和十八个属社区分别在 NC、ON 和 OP 组中富集。Spearman 相关分析表明, 属的丰度与腰椎 BMD 和 T 评分呈正相关(<0.05)。功能预测显示,NC 组中与氨基酸合成、维生素合成和核苷酸代谢相关的途径富集,而 ON 和 OP 组中主要富集与代谢物降解和碳水化合物代谢相关的途径。
本研究结果为肠道微生物群与绝经后骨丢失之间的关系提供了新的流行病学证据,为进一步探索预防和治疗绝经后骨质疏松症(PMO)的治疗靶点奠定了基础。