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Gut microbiota and metabolite alterations associated with reduced bone mineral density or bone metabolic indexes in postmenopausal osteoporosis

机译:绝经后骨质疏松症的肠道菌群和代谢物改变与降低的骨矿物质密度或骨代谢指标有关

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摘要

Reduced bone mineral density (BMD) is associated with an altered microbiota in senile osteoporosis. However, the relationship among gut microbiota, BMD and bone metabolic indexes remains unknown in postmenopausal osteoporosis. In this study, fecal microbiota profiles for 106 postmenopausal individuals with osteopenia (n=33) or osteoporosis (n=42) or with normal BMD (n=31) were determined. An integrated 16S rRNA gene sequencing and LC-MS-based metabolomics approach was applied to explore the association of estrogen-reduced osteoporosis with the gut microbiota and fecal metabolic phenotype. Adjustments were made using several statistical models for potential confounding variables identified from the literature. The results demonstrated decreased bacterial richness and diversity in postmenopausal osteoporosis. Additionally, showed significant differences in abundance levels among phyla and genera in the gut microbial community were found. Moreover, postmenopausal osteopenia-enriched N-acetylmannosamine correlated negatively with BMD, and distinguishing metabolites were closely associated with gut bacterial variation. Both serum procollagen type I N propeptide (P1NP) and C-terminal telopeptide of type I collagen (CTX-1) correlated positively with osteopenia-enriched , and . However, we did not find a significant correlation between bacterial diversity and estrogen. These observations will lead to a better understanding of the relationship between bone homeostasis and the microbiota in postmenopausal osteoporosis.
机译:降低的骨矿物质密度(BMD)与老年性骨质疏松症中的微生物群改变有关。然而,绝经后骨质疏松症中肠道菌群,骨密度和骨代谢指标之间的关系仍然未知。在这项研究中,确定了106名绝经后患有骨质疏松症(n = 33)或骨质疏松症(n = 42)或BMD正常(n = 31)的人的粪便微生物区系。整合的16S rRNA基因测序和基于LC-MS的代谢组学方法被用于探讨雌激素减少的骨质疏松症与肠道菌群和粪便代谢表型的关系。使用几种统计模型对从文献中识别出的潜在混杂变量进行了调整。结果表明,绝经后骨质疏松症的细菌丰富度和多样性降低。此外,发现肠道微生物群落的门和属之间的丰度水平存在显着差异。此外,绝经后富含骨质减少的N-乙酰甘露糖胺与BMD呈负相关,并且可区分的代谢产物与肠道细菌变异密切相关。血清I型胶原蛋白原胶原(P1NP)和I型胶原蛋白的C末端端肽(CTX-1)与骨质疏松症增生呈正相关。但是,我们没有发现细菌多样性和雌激素之间的显着相关性。这些观察结果将使人们更好地了解绝经后骨质疏松症中骨稳态与微生物群之间的关系。

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