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Gut Microbiota Alterations in Postmenopausal Women with Osteoporosis and Osteopenia from Shanghai, China

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Journal PeerJ
Date 2024 Jun 4
PMID 38832037
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Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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).

Citing Articles

Mechanisms of gut homeostasis regulating Th17/Treg cell balance in PMOP.

Qi P, Xie R, Liu H, Zhang Z, Cheng Y, Ma J Front Immunol. 2024; 15:1497311.

PMID: 39735544 PMC: 11671525. DOI: 10.3389/fimmu.2024.1497311.

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