School of Electronics and Information, Northwestern Polytechnical University, Xi'an, China.
Clinical Laboratory of Honghui Hospital, Xi'an Jiaotong University, Xi'an, China.
Front Cell Infect Microbiol. 2022 Mar 31;12:827575. doi: 10.3389/fcimb.2022.827575. eCollection 2022.
Osteoporosis (OP), clinically featured with a low bone mineral density (BMD) and high risk of bone fracture, has become a major risk factor of disability and death in the elders, especially in postmenopausal women. The gut microbiome (GM) is thought to be implicated in bone metabolism. Herein, we clarified the composition signature and gene functional profile of GM in older people with normal and low BMD.
A total of 455 participants underwent the BMD measurement and biochemical detection. GM analysis was further performed on 113 cases of postmenopausal women and men aged over 50, including both 16S rRNA and metagenomic sequencing.
Generally, the BMD value was significantly lower in the older age groups, especially in the postmenopausal women. Consistently, we observed obvious vitamin D deficiency or insufficiency in females (compared to the male, < 0.0001). The results from 16S rRNA sequencing revealed higher numbers of OTUs and diversity indexes in females than in males. The abundance in composition of and were correlated with the BMD values in females. LEfSe analysis discovered several enriched bacteria taxons in OP and normal control (NC) subgroups. A positive correlation between the number of genes and BMD values was observed in females based on metagenomic sequencing analysis. Furthermore, we identified the connecting modules among the GM composition - gene functional signature - BMD value/T score in both females and males.
This study provides evidences upon which to understand the mechanisms of the effects of GM on bone health, consequently revealing the physiology status and potential diagnostic/therapeutic targets based on GM for OP and postmenopausal osteoporosis (PMOP). Besides, the status of vitamin D deficiency or insufficiency need to be concerned and improved in the Chinese people.
骨质疏松症(OP)的临床特征是骨矿物质密度(BMD)低,骨折风险高,已成为老年人,尤其是绝经后妇女残疾和死亡的主要危险因素。肠道微生物群(GM)被认为与骨代谢有关。本研究旨在阐明骨密度正常和低的老年人肠道微生物群的组成特征和基因功能谱。
共 455 名参与者接受了 BMD 测量和生化检测。进一步对 113 名年龄在 50 岁以上的绝经后妇女和男性进行 GM 分析,包括 16S rRNA 和宏基因组测序。
一般来说,随着年龄的增长,BMD 值明显降低,尤其是绝经后女性。同样,我们观察到女性维生素 D 缺乏或不足明显(与男性相比,<0.0001)。16S rRNA 测序结果显示,女性的 OTU 数量和多样性指数明显高于男性。和的组成丰度与女性的 BMD 值相关。LEfSe 分析发现 OP 和正常对照组(NC)亚组中存在几种富集细菌分类群。基于宏基因组测序分析,女性的基因数量与 BMD 值呈正相关。此外,我们在女性和男性中确定了 GM 组成-基因功能特征-BMD 值/T 评分之间的连接模块。
本研究为理解 GM 对骨骼健康影响的机制提供了依据,从而揭示了基于 GM 的 OP 和绝经后骨质疏松症(PMOP)的生理状态和潜在诊断/治疗靶点。此外,中国人需要关注和改善维生素 D 缺乏或不足的状况。