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Association of gut microbiota composition and function with an aged rat model of senile osteoporosis using 16S rRNA and metagenomic sequencing analysis

机译:肠道微生物群组成和功能与老年大鼠骨质疏松症的16S rRNA和宏基因组测序分析的关联

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摘要

Recently, more interest has been paid to the association between bone mass and gut microecological dysbiosis. The results of clinical studies comparing gut microbiota (GM) in osteoporosis patients have been inconsistent due to different inclusion and exclusion criteria. To date, the association between the GM and senile osteoporosis remains poorly understood. Here, we utilized an aged rat model (22 months old) of senile osteoporosis to study the association of the composition and function of the GM with osteoporosis by 16S rRNA and metagenomic sequencing. The results showed that there was a significant reduction in alpha diversity and the F/B ( ) ratio in aged rats. At the genus level, the enrichment of was potentially related to osteoporosis as a risk factor. Metagenomics results based on two databases indicated that shifts in the GM contribute to senile osteoporosis through metabolic pathways and subsequent immune disorders. In conclusion, our study reveals the association of gut microbiota composition and function with senile osteoporosis in an aged rat model in a brand new way, and variations in the GM might contribute to senile osteoporosis through metabolic pathways.
机译:最近,人们对骨量与肠道微生态失调之间的联系有了更多的兴趣。由于纳入和排除标准的不同,比较骨质疏松症患者肠道菌群(GM)的临床研究结果不一致。迄今为止,对转基因与老年性骨质疏松症之间的关联仍然知之甚少。在这里,我们利用老年大鼠骨质疏松症的一个老年大鼠模型(22个月大)通过16S rRNA和宏基因组测序研究了GM与骨质疏松症的组成和功能的关联。结果表明,老年大鼠的α多样性和F / B()比有显着降低。在属水平上,的富集可能与骨质疏松症有关,是危险因素。基于两个数据库的元基因组学结果表明,GM的变化通过代谢途径和随后的免疫疾病导致了老年性骨质疏松症。总之,我们的研究以全新的方式揭示了老年大鼠模型中肠道菌群组成和功能与老年性骨质疏松的关系,而GM的变化可能通过代谢途径促进老年性骨质疏松。

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